Dome Patent, L.P. v. Rea

UNITED STATES DISTRICT COURT
FOR THE DISTRICT OF COLUMBIA

_________________________________________
)
DOME PATENT, L.P., )
)
Plaintiff, )
)
v. ) Civil Action No. 07-1695 (PLF)
)
TERESA STANEK REA, Acting Under Secretary )
of Commerce for Intellectual Property and )
Acting Director of the United States Patent )
and Trademark Office, )
)
Defendant.1 )
_________________________________________ )

OPINION, FINDINGS OF FACT AND CONCLUSIONS OF LAW

Dome Patent L.P. owns United States Patent No. 4,306,042 (the “Neefe Patent”),

which was issued on December 15, 1981. The Neefe Patent is entitled “Method of Making a

Contact Lens Material With Increased Oxygen Permeability,” and it is based on an application

filed by Russell A. Neefe. See JTX-1. In 2007, the United States Patent and Trademark Office

(the “PTO”) found that claim 1 of the Neefe Patent should be cancelled as obvious in light of the

prior art. Dome timely filed a civil complaint under 35 U.S.C. §§ 145 and 306, requesting that

this Court set aside the PTO’s decision. See Compl. ¶ 20. After considering the parties’

arguments, the administrative record, the decision of the PTO’s Board of Patent Appeals and

Interferences, the evidence presented during a three-day bench trial, and the relevant legal

authorities, the Court concludes that the process recited in claim 1 of the Neefe Patent is

1
Pursuant to Rule 25(d) of the Federal Rules of Civil Procedure, the Court
substitutes as defendant the acting Under Secretary, Teresa Stanek Rea, for the former Under
Secretary, David J. Kappos.
unpatentable, as it would have been obvious to a person of ordinary skill in the art at the time the

patent application was filed. The Court therefore will enter judgment in favor of the defendant,

Teresa Stanek Rea (“the Director”), Acting Under Secretary of Commerce for Intellectual

Property and Acting Director of the PTO.1

I. BACKGROUND

A. The Neefe Patent and the Procedural History

The Neefe Patent contains four claims, the first of which is relevant to this action.

Claim 1 recites:

1
The exhibits presented at trial – Joint Trial Exhibits (“JTX”) 1-34, Plaintiff’s Trial
Exhibits (“PTX”) 1-6, and Defendant’s Trial Exhibits (“DTX”) 1-2 – are listed in the appendix to
this decision. In addition, the Court reviewed the following papers in connection with this
matter: the complaint (“Compl.”) [Dkt. No. 1]; defendant’s answer [Dkt. No. 4]; plaintiff’s trial
brief (“Dome’s Trial Brief”) [Dkt. Nos. 54/52 (sealed/public)]; defendant’s response to
plaintiff’s trial brief (“Director’s Trial Brief”) [Dkt. Nos. 57/59]; plaintiff’s reply trial brief [Dkt.
Nos. 65/71]; the parties’ joint pretrial statement (“Jt. Pretrial Stmt.”) [Dkt. Nos. 61/62];
defendant’s motion in limine to exclude the testimony of Dr. Melamed pursuant to Fed. R. Evid.
702 [Dkt. Nos. 70/67]; plaintiff’s opposition to defendant’s motion to exclude the testimony of
Dr. Melamed [Dkt. Nos. 76/79]; defendant’s reply in support of her motion in limine to exclude
the testimony of Dr. Melamed [Dkt. Nos. 82/85]; defendant’s motion in limine to exclude the
testimony of Dr. Melamed and portions of the testimony of Dr. Long pursuant to Fed. R. Evid.
401 [Dkt. Nos. 69/66]; plaintiff’s opposition to motion in limine to exclude the testimony of Dr.
Melamed and portions of the testimony of Dr. Long [Dkt. Nos. 77/80]; defendant’s reply to
opposition to motion in limine to exclude the testimony of Dr. Melamed and portions of the
testimony of Dr. Long [Dkt. Nos. 83/84]; plaintiff’s surreply in opposition to motion in limine to
exclude testimony of Dr. Melamed and portions of the testimony of Dr. Long [Dkt. Nos. 89, 88];
plaintiff’s supplemental trial brief [Dkt. No. 81]; defendant’s brief in response to plaintiff’s
supplemental trial brief [Dkt. No. 87]; plaintiff’s reply supplemental trial brief [Dkt. No. 91];
defendant’s proposed findings of fact and conclusions of law (“Director’s PFF.” or “Director’s
Prop. Concl. of Law,” as appropriate) [Dkt. No. 100]; plaintiff’s proposed findings of fact and
conclusions of law (“Dome’s PFF.” or “Dome’s Prop. Concl. of Law,” as appropriate);
defendant’s response to plaintiff’s proposed findings of fact and conclusions of law (“Director’s
Resp. PFF.” or “Director’s Resp. Concl. of Law,” as appropriate) [Dkt. No. 104]; plaintiff’s
response to defendant’s proposed findings of fact and conclusions of law (“Dome’s Resp. PFF.”
or “Dome’s Resp. Concl. of Law,” as appropriate) [Dkt. No. 105]; and transcripts of the January
15, 2013 pretrial conference and of the bench trial held from January 28 through January 30,
2013, designated by way of example as “Jan. 28 AM Tr.”.
2
 A method of making an oxygen permeable material for the
manufacture of contact lens [sic] by the synthesization of the
monomer 1,1,1-tris(methylsiloxy)methacryloxypropylsilane (a
siloxanyl alkyl ester) by the following procedures:

(a) a mixture is prepared having the relationship of one
mole of methacryloxypropyltrimethoxysilane with three to forty
moles of trimethylchlorosilane;

(b) the mixture is then added to water whose volume is
from 3 to 10 times that of the mixture;

(c) agitation is maintained for 30 minutes to 48 hours;

(d) then allow the mixture to separate into layers, remove
and filter the upper organic layer;

(e) the unwanted by-product (hexamethyldisiloxane) is then
removed by vacuum distillation;

(f) forming an oxygen permeable contact lens material by
copolymerizing from 5% to 90% by weight of the 1,1,1
tris(trimethylsiloxy)methacryloxypropyl-silane prepared above;
3% to 90% by weight of an ester of acrylic or methacrylic acid;
from 0.5% to 90% by weight of a surface wetting agent, from
0.01% to 90% by weight of an oxygen permeable crosslinking
agent selected from the class of multifunctional siloxanyl alkyl
esters in the presence of a free radical or a photo initiator.

JTX-1 at col.5 lines 38-64 (emphasis added); id., Certificate of Correction. Steps (a) through (e)

of this claim recite a process for manufacturing a chemical compound commonly known as

“Tris.” Step (f) describes a process for synthesizing Tris with three other compounds to create a

rigid, gas permeable material suitable for manufacturing a contact lens.2

In December 1997, Dome sought to enforce the Neefe Patent in an infringement

action against several defendants. See Dome Patent L.P. v. Permeable Technologies, Inc., et al.,

Civil Action No. 98-6247 (filed in the Western District of New York, after being transferred

2
The first underlined term refers to a chemical compound commonly known as
“Tris.” The second underlined term refers to a Tris-type cross-linking agent.
3
from the Eastern District of California). One of these defendants, Optical Polymer Research,

Inc., filed a request with the PTO for reexamination of the Neefe Patent. JTX-34 at 53-95

(Request for Reexamination, Aug. 27, 1998). On May 23, 2002, an examiner at the PTO

concluded that claims 2, 3, and 4 of the Neefe Patent should be confirmed, but that claim 1 of the

Neefe Patent – recited above – should be cancelled because the method it described “would have

been obvious at the time the invention was made to a person having ordinary skill in the art.” 35

U.S.C. § 103(a); JTX-34 at 1110-20 (Office Action in Ex Parte Reexamination). Dome timely

appealed the examiner’s ruling to the Board of Patent Appeals and Interferences (the “Board”).

JTX-34 at 1134-35 (Notice of Appeal dated July 12, 2002).3 On July 31, 2007, the Board issued

an order affirming the examiner’s decision. JTX-34 at 1270-93 (In re Neefe, Appeal 2007-

1366).

On September 24, 2007, Dome timely filed this civil action pursuant to 35 U.S.C.

§§ 145 and 306 for review of the Board’s decision. Compl.; Jt. Pretrial Stmt. at 3. The Court

conducted a three-day bench trial from January 28 through January 30, 2013, during which the

parties introduced the expert testimony of Timothy E. Long, Ph.D., Mark A. Melamed, M.D.,

and William J. Benjamin, O.D., Ph.D., as well as testimony from the patent’s author, Robert A.

Neefe. Dr. Long, called as a witness by Dome, is a professor of chemistry at the Virginia

Polytechnic Institute and State University and an expert in the field of polymer chemistry. Dr.

Melamed, also Dome’s witness, is an ophthalmologist with a large private practice in which he

spends a substantial part of his time prescribing and fitting contact lenses. He also is a Professor

of Ophthalmology at New York University School of Medicine. Dr. Melamed is an expert on

the use and prescription of rigid gas permeable contact lenses and on the medical benefits of

3
The Board is now known as the Patent Trial and Appeal Board.

4
contact lenses with improved oxygen permeability.4 The Director’s expert, Dr. Benjamin, is a

Professor of Optometry and Vision Science at the University of Alabama School of Optometry.

He is an expert in the measurement of the oxygen permeability of contact lenses and the

wettability of rigid contact lenses.5

B. The Parties’ Positions

As discussed in the Findings of Fact below, many of the relevant facts in this case

are undisputed. The parties agree that a usable hard contact lens must be clear, rigid, oxygen

permeable, and wettable (i.e., hydrophilic). The parties also agree that the field of contact lens

development witnessed a breakthrough in the 1970’s with the advent of rigid gas permeable

lenses, which combined the clarity, rigidity, and wettability of one prior technology (PMMA

lenses) with the oxygen permeability of another prior technology (soft silicone lenses). One of

the lead inventors in this field, Norman Gaylord in New Providence, New Jersey, created the first

commercially viable rigid gas permeable lens material using a novel “polymer,” composed of

4
The Director filed a motion in limine to exclude the testimony of Dr. Melamed
relating to the commercial success of Bausch & Lomb’s Boston IV lens pursuant to Rule 702 of
the Federal Rules of Evidence. Because the purpose of Rule 702 and Daubert v. Merrell Dow
Pharm., Inc., 509 U.S. 579 (1993) is for the judge to serve a gatekeeping role for the jury, see
Jacobsen v. Oliver, Civil Action No. 01-1810, 2007 WL 5527513, at *1 (D.D.C. Nov. 2, 2007)
(collecting cases), the Court declined to exclude Dr. Melamed’s testimony during this non-jury
trial. See Jan. 15 AM Tr. at 33:24–34:06. But the Court has given little weight to Dr.
Melamed’s testimony relating to the reasons for the Boston IV lens’ commercial success, as his
opinion on this matter is not based on any study, survey, or reliable methodology, but is simply
based on his experience with his own patients.
5
The Court granted Dome’s motion during trial to exclude those portions of Dr.
Benjamin’s testimony relating to the polymer chemistry underlying contact lens production, as
this topic does not fall within the scope of Dr. Benjamin’s expertise. Goodman v. Harris
Cnty., 571 F.3d 388, 399 (5th Cir. 2009) (an expert may not “go beyond the scope of his
expertise in giving his opinion”); Sosna v. Binnington, 321 F.3d 742, 746 (8th Cir. 2003) (same).

5
different “monomers.” In making this polymer, Gaylord began by using a silicone-containing

monomer called Tris, which is very oxygen permeable but not wettable (that is, it is

hydrophobic). Gaylord next added other monomers similar to those used in PMMA lenses,

which are highly wettable but not oxygen permeable. Gaylord then joined the hydrophobic Tris

monomers and the hydrophilic comonomers together, using a hydrophilic cross-linking agent.

This material could then be machined into a reasonably usable contact lens. Several other

scientists subsequently refined and expanded on Gaylord’s invention.

A few years later, a group of scientists led by Kyoichi Tanaka in Japan patented a

different rigid gas permeable contact lens material using a non-Tris monomer with a range of

cross-linking agents. One of Tanaka’s preferred cross-linkers was a hydrophobic multifunctional

siloxanyl alkyl ester, which is similar in molecular structure to the Tris monomer.

Less than two years later, Robert Neefe of Big Spring, Texas, combined the

monomers used by Gaylord with the cross-linker used by Tanaka to develop a usable rigid gas

permeable lens. Neefe’s process was patented as claim 1 of U.S. Patent No. 4,306,042, recited

above and referred to here as the Neefe Patent.

This case centers on the parties’ disagreement as to whether it would have

occurred to a person of ordinary skill in the art to do what Neefe did: to combine the first three

compounds listed in step (f) of claim 1 of the Neefe Patent – i.e., Gaylord’s compounds – with

the fourth compound listed in step (f) – i.e., Tanaka’s cross-linker. Dome contends that it would

not have occurred to a person of ordinary skill to attempt this combination. According to Dome,

one with ordinary skill would have been deterred from using both the Tris monomer from

Gaylord and the Tris-type cross-linker from Tanaka in the same formulation, out of concern that

the resulting compound would be unwettable or otherwise unusable for contact lens production.

6
See Dome’s Trial Brief at 10 (“[U]sing both a hydrophobic Tris monomer and a hydrophobic

cross-linker would have been expected to yield a hydrophobic polymer that would be unsuitable

as a contact lens material.”); id. at 9 (“Neefe offered a novel and counter-intuitive solution to the

oxygen permeability problem: a polymer that contains both a hydrophobic Tris monomer and a

hydrophobic Tris-type cross-linker.”) (emphasis in original). Dome also attempts to show that

the success of a commercial contact lens made using the Neefe process demonstrates the

nonobviousness of that process, supporting its patentability. Id. at 1 (describing evidence of

“surprising and counter-intuitive results achieved by the method disclosed and claimed in the

Neefe Patent” and “evidence of large scale commercial exploitation and use of the method

disclosed and claimed in the Neefe Patent”).

The Director disagrees, arguing that it was established that the hydrophobicity of

both the Tris monomer and the Tris-type cross-linker could be offset by the hydrophilic

monomers suggested by Gaylord, particularly within the broad ranges identified by Neefe. See

Director’s Trial Brief at 28 (“Any concern about wettability arising from the use of a small

amount of Tris (as low as 5% by weight), therefore, easily could be alleviated by use of a wetting

agent (up to 90% by weight), while still remaining within the scope of the claim.”). And while

the Director does not dispute that the contact lens referenced by Dome was commercially

successful, she argues that this success cannot be attributed to the Neefe process for several

reasons, and therefore any evidence of success is irrelevant to the question of obviousness. See

id. at 5-7, 13-14, 16-25.

7
 II. FINDINGS OF FACT

The following findings of fact are based on the evidence submitted by the parties

during the bench trial, the administrative record before the Board, the Board’s opinion, the

parties’ stipulations of undisputed facts, and the record as a whole.

A. The Polymer Chemistry of Contact Lens Material Production

a. Properties of Rigid Gas Permeable Contact Lenses

1. Claim 1 of the Neefe Patent recites a process for making material for the

manufacture of a rigid gas permeable (“RGP”) contact lens. JTX-1 at [57] (Abstract).

2. A material for use in a RGP contact lens should have the following four

characteristics: it should be optically clear; it should be hard and rigid; it should be wettable; and

it should be oxygen permeable. Jan. 28 AM Tr. at 49:8–50:13 (Long); Jan. 29 AM Tr. at 14:25–

16:7, 17:2-21, 100:9-11 (Melamed); Jan. 29 PM Tr. at 48:3-11 (Benjamin).

3. Optical clarity is important in order for the material to provide a clear visual

image for the user. See Jan. 28 AM Tr. at 49:8-10 (Long); Jan. 29 PM Tr. at 48:3-7 (Benjamin).

4. Rigidity is required so that the lens can be machineable into a precise enough

shape to provide crisp, consistent visual acuity. Jan. 28 AM Tr. at 49:16-21 (Long); Jan. 29 PM

Tr. at 48:3, 48:7-11 (Benjamin).

5. Wettability, which is the interaction of water with a surface (such as the surface of

a contact lens), is necessary for a contact lens to be comfortable on the eye of the wearer. Jan. 28

AM Tr. at 50:7-13 (Long); Jan. 29 AM Tr. at 15:12–16:7, 17:7-9 (Melamed).

6. Wettability is important because contact lenses do not actually sit on the surface

of the cornea of the eye; instead, they float on a thin film of tears on the surface of the cornea.

Jan. 29 AM Tr. at 14:12-14 & 15:19-23 (Melamed). Contact lenses must be tolerated in the eye

8
without eliciting a painful foreign body sensation, so an even coating of tears must be spread

across the surface of the lens. Id. at 15:12–16:3 (Melamed).

7. A hydrophobic polymer is one that is water repellent, while a hydrophilic

polymer can readily absorb water. Jan. 28 AM Tr. at 10:2 (Long); Jan. 30 AM Tr. at 13:25

(Benjamin).

8. Adequate oxygen permeability is necessary to prevent long-term damage to the

eye of the wearer. Jan. 28 AM Tr. at 49:22–50:6 (Long); Jan. 29 AM Tr. at 14:25–15:11, 17:2-6,

17:19-21, 100:9-11 (Melamed).

9. Oxygen permeability is important because a constant flow of oxygen to the cornea

is essential to avoid degenerative changes in its cells. Jan. 29 AM Tr. at 14:25–15:11

(Melamed). The cornea has no blood supply to bring it oxygen, so it gets its oxygen from the

atmosphere, through the open lids of the eye. Jan. 29 AM Tr. at 14:14-17 (Melamed).

10. Anything that covers the cornea – either a contact lens or the eyelid – impedes the

flow of oxygen to the cornea. Jan. 29 AM Tr. at 14:17-20 (Melamed). Thus, the oxygen flow to

the cornea is impeded during sleep. Id. at 16:10-21 (Melamed).

11. Even with a contact lens in place, oxygen can reach the front surface of the cornea

in two ways: (1) it can permeate through the body of the contact lens itself; or (2) it can be

carried by tears around the edge of the contact lens. Jan. 29 AM Tr. at 14:20-24 (Melamed).

12. The oxygen permeability of a material is measured in Dk, or “barrers.” JTX-4 at

62; Jan. 29 AM Tr. at 25:22-23 (Melamed); Jan. 30 AM Tr. at 35:25 (Benjamin).

13. Ideally, a contact lens material will meet all four criteria: clarity, hardness,

oxygen permeability, and wettability. Jan. 28 AM Tr. at 53:21-24 (Long). As Dome’s counsel

9
noted at trial, these criteria can be remembered with the acronym “CHOW.” Jan. 28 AM Tr. at

9:7-8; see also Jan. 28 AM Tr. at 48:16-17 (Long).

b. The Polymer Chemistry Behind Contact Lens Manufacturing

14. The technology at issue in this case is the polymer chemistry required to

manufacture RGP contact lenses.

15. A RGP contact lens is made from material that permits the passage of oxygen

through the lens to the eye of the wearer. Jan. 29 AM Tr. at 40:9-10 (Melamed); JTX-4 at 63.

16. A “polymer,” also known as a “macromolecule,” is a large molecule made up of

many smaller units called “monomers.” JTX-3 at 3.

17. The process of synthesizing a polymer from monomers is called

“polymerization.” JTX-3 at 3.

18. A “copolymer” is a type of polymer that is formed from two or more different

types of monomers. JTX-3 at 7.

19. The process of synthesizing a copolymer is known as “copolymerization.”

PTX-4, at tab 2; Director’s PFF. 14.

20. Polymers can take different forms, including linear, branched, and cross-linked

(i.e., networked). JTX-3 at 8-10. Illustrative examples of these different forms were provided at

trial and are reproduced below. See PTX-4 at Tab 3; Jan. 28 AM Tr. at 57:10-63:20 (Long).

10
 21. The materials that make up a polymer can alter the polymer’s chemical structure

and therefore its physical properties. Jan. 28 AM Tr. at 63:1-20 (Long).

22. For example, the use of one cross-linking agent instead of another can affect the

size of the gaps in the polymer’s structure, which can affect the polymer’s oxygen permeability.

Jan. 28 AM Tr. at 62:3-63:20 (Long).

23. Cross-linked polymers can be exceptionally complex; the cross-linking agents

may be close together or far apart, short or long, few or plentiful. Jan. 28 AM Tr. at 61:8-22

(Long).

B. The Prior Art: The Comonomers Used by Neefe Were Known in the Prior Art and, When
Used in Combination, Could Be Expected to Promote Oxygen Permeability

This case centers on a dispute about whether Neefe’s invention would have been

obvious to a person of ordinary skill in the art, in light of the technology existing and known in

the field at the time of Neefe’s invention – i.e., the prior art. Although the facts discussed in the

section below are undisputed, the Court makes the following findings relating to the prior art and

the Neefe Patent, with the purpose of providing background and context.6

6
Some of the facts in Section B (FF. 24-89) are dismissed by one party or the other
as irrelevant or misleading, but there are no genuine disputes as to their factual accuracy.
11
 a. The Prior Art

24. The first practical plastic contact lens was made out of polymethyl methacrylate

(“PMMA”), which was first branded commercially as Plexiglas. See Jan. 28 AM Tr. at 50:25-

51:1 (Long); Jan. 30 AM Tr. at 12:2-18 (Benjamin).

25. PMMA is a rigid, glass-like thermoplastic with relatively little flexibility. Jan. 28

AM Tr. at 51:9-10 (Long), 70:17-18; JTX-4 at 61-62.

26. PMMA is highly wettable, but it also is completely impermeable to oxygen. See

Jan. 28 AM Tr. at 51:13-21 (Long); Jan. 30 AM Tr. at 12:2-18 (Benjamin).

27. This lack of oxygen permeability of PMMA lenses led to the development of so-

called “contact lens over-wear syndrome” in users. Wearing these lenses for an extended period

of time could cause pain, death of nerve endings in the cornea, blurred or filmy vision, glare, and

halos around lights. Jan. 29 AM Tr. at 15:2-9 (Melamed); see also JTX-10 at col.1 lines 28-32;

Jan. 30 AM Tr. at 16:10-21 (Benjamin); JTX-27 at 279.

28. In response to the problem of contact lens over-wear, many scientists began

exploring polymers containing siloxanes for use in contact lens materials. Jan. 28 AM Tr. at

51:22–53:24 (Long); JTX-4 at 7, 60-63.

29. Siloxanes are chemical compounds containing carbon atoms (C), oxygen atoms

(O), and silicon atoms (Si), in which two silicon atoms are bonded directly to one oxygen atom

in the form –Si–O–Si–. JTX-4 at 60-62. The –Si–O–Si– chain can be thought of as the

polymer’s backbone, to which other atoms and molecules are attached. Id.

12
PTX-4 at tab 8.

30. Siloxanes are highly oxygen permeable. They also, however, are hydrophobic –

that is, water repellant. In addition, siloxanes are soft and difficult to machine. Jan. 28 AM Tr.

at 52:10-25 (Long); Jan. 30 AM Tr. at 13:22-23 (Benjamin); JTX-4 at 17, 61-62; JTX-5 at 272;

JTX-13 at col.1 lines 33-34, 40-43.

31. A significant breakthrough in the field of contact lens materials took place in the

1970’s, when Norman G. Gaylord had the idea of using a rigid material for a contact lens that

still allowed oxygen to pass through the lens to reach the cornea of the eye. Gaylord introduced

the first RGP lens, an oxygen permeable contact lens made from a mixture of PMMA and

silicone (siloxane). JTX-4 at 17; Jan. 29 AM Tr. at 22:24-25 (Melamed); id. at 53:19-24

(Melamed); see JTX-7; JTX-8.

32. In his invention, Gaylord combined four ingredients: (i) a silicone -based

monomer; (ii) an acrylate; (iii) a wetting agent; and (iv) a cross-linking agent. Jan. 28 AM Tr. at

70:18-23 (Long); JTX-4 at 64; JTX-7 at col.1 lines 57-60; JTX-8 at col.1 lines 52-56, col.5 lines

39-46, col.6 lines 3-12; see Board Decision, JTX-16 at F.10.

33. In Gaylord’s polymer, the silicone is the chemical compound 1,1,1-

tris(trimethylsiloxy)methacryloxypropylsilane, which is commonly known in the contact lens

13
field as a “Tris” monomer. Jan. 28 AM Tr. at 69:11-70:5 (Long); JTX-1 at col.3 lines 13-14;

JTX-4 at 63; JTX-7 at col.2 lines 26-35; JTX-8 at col.2 lines 32-44.

34. After Gaylord, the Tris monomer became the “industry standard” siloxy-

methacrylate monomer in the field of RGP contact lenses. JTX-4 at 63.

35. Tris is a siloxanyl alkyl ester compound. Jan. 28 PM Tr. at 66:8 (Long); JTX-1 at

col.3 lines 12-14, col.5 lines 40-41.7

36. Tris is very hydrophobic, i.e., water repellant. Jan. 28 AM Tr. at 66:2-4, 74:20-21

(Long); JTX-6 at col.1 lines 63-66.

37. In addition to Tris, Gaylord used methyl methacrylate (“MMA,” the monomer in

PMMA) as the acrylate, and he employed methacrylic acid as the wetting agent. Both MMA and

methacrylic acid are hydrophilic: these comonomers therefore increased the wettability of the

polymer. Jan. 28 AM Tr. at 67:3-12 (Long); Jan. 28 PM Tr. at 68:14-21 (Long); JTX-7 at col.3

line 29, col.4 lines 50-59; JTX-8 at col.3 line 65, col.5 lines 39-48; see also JTX-4 at 17.

38. The fourth ingredient, which Gaylord used to bind these comonomers together,

was a hydrophilic, non-siloxane based cross-linking agent, such as ethylene glycol

dimethacrylate. Jan. 28 AM Tr. at 70:9-13 (Long); PTX-4 at Tab 9.

39. Contact lenses manufactured using the Gaylord polymer were introduced into the

marketplace in the late 1970’s by Syntex, Inc. under the trade name Polycon. Jan. 30 AM Tr. at

40:2-7 (Benjamin); JTX-4 at 17; JTX-10 at col.2 lines 29-32; JTX-12 at 238.

40. The first Polycon lens (Polycon I) had an oxygen permeability of approximately 5

Dk; the second (Polycon II), an oxygen permeability of approximately 10 to 12 Dk. The Polycon

7
Tris was first disclosed by George J. Quaal in U.S. Patent No. 3,377,371 (issued
April 9, 1968). JTX-6 at 1.
14
lenses thus exhibited much better oxygen permeability than PMMA lenses, which were

completely impermeable. JTX-4 at 67; JTX-12 at 238; JTX-27 at 273.

41. Gaylord explains that the reason for the increased oxygen permeability of his lens

materials is the inclusion of silicone (i.e., the use of the siloxanyl alkyl ester), which “is highly

permeable to oxygen.” JTX-8 at col.1 lines 31-32; see generally id. at col.1 lines 19-56.

42. At noted at FF. 30 and 36, although the presence of silicone improves the oxygen

permeability of a contact lens material, it detracts from its wettability.

43. Gaylord addresses the issue of wettability in his patent. He states that “[w]hile

some of the copolymers [disclosed in his patent] are inherently wettable by human tears, it may

be necessary to improve the wettability of others.” JTX-8 at col.5 lines 39-41.

44. Gaylord discloses four alternate methods for improving the wettability of these

copolymers, including adding hydrophilic monomers to the copolymerization mixture and

applying wetting agents to the surface of the contact lenses. JTX-8 at col.5 lines 42-58.

45. Although Gaylord’s invention represented a significant improvement in oxygen

permeability, the first lenses incorporating Gaylord’s polymer still could not be used for

prolonged daily wear. See Jan. 29 AM Tr. at 91:13–92:8 (Melamed).

46. After Gaylord’s technique was known, several scientists worked to increase the

oxygen permeability, wettability, and hardness of Gaylord’s formulation. See Jan. 28 AM Tr. at

73:10–79:10 (Long); see, e.g., JTX-9 at col.1 lines 11-41.

47. One pair of scientists – Edward J. Ellis and Joseph C. Salamone at Polymer

Technology Corporation in Massachusetts – improved Gaylord’s technique by employing Tris

but also adding an additional hydrophilic comonomer to improve the material’s wettability and

15
structural integrity. Jan. 28 AM Tr. at 73:20–74:21 (Long); see generally JTX-9. Ellis applied

for a patent based on this invention on February 15, 1978. JTX-9 at [22].

48. The Ellis patent was issued on May 1, 1979. It was later used to create the Boston

II lens, which had an oxygen permeability of approximately 12 to 14 Dk. JTX-9 at [45]; Jan. 29

AM Tr. at 25:22-25, 54:4-9 (Melamed); Jan. 30 AM Tr. at 69:25–70:2, 75:21-25 (Benjamin);

JTX-4 at 66; JTX-12 at 238; JTX-21 at BL8556; JTX-27 at 273.

49. Another scientist, Nick N. Novicky of Wheeling, Illinois, attempted to solve the

problems of the Gaylord polymers by replacing the Tris monomer with novel silicones of his

own design. Jan. 28 AM Tr. at 75:23-25 (Long); see JTX-11 at col.3 lines 22-23, col.14 lines

37-45, col.18 lines 8-13.

50. Like Tris, the novel monomer employed by Novicky contains a methacrylate

component and a tris(trimethylsiloxy) component. Jan. 28 AM Tr. at 76:22–77:9 (Long);

JTX-11 at col.3 lines 49-53, col.3 lines 64-67, col.4 lines 25-39 (general formula), col.18 lines

28-39 (formula in claim 1).

51. Unlike Tris, the Novicky monomer contains an additional siloxane unit. JTX-11

at col.4 lines 25-39, col.18 lines 28-39; Jan. 28 AM Tr. at 76:1-4, 77:7-9 (Long).

52. This additional siloxane unit makes the novel Novicky monomer even more

hydrophobic than Tris. Jan. 28 AM Tr. at 75:22-76:12 (Long).

53. In addition to the novel monomer, Novicky’s polymer also contains hydrophilic

wetting agents and hydrophilic MMA. JTX-11 at col.3 lines 44-48, col.6 line 65, col.7 line 27,

col.18 lines 66-68, col.19 lines 1-3.

16
 54. The Novicky polymer uses the same type of hydrophilic cross-linker used by

Gaylord and Ellis; as noted supra at FF. 38, this cross-linker does not contain a siloxane group.

JTX-11 at col.7 lines 15-24; Jan. 28 AM Tr. at 77:12-18 (Long).

55. The Novicky patent was issued on August 5, 1980. JTX-11 at [45].

56. RGP contact lenses incorporating the Novicky polymer reportedly were marketed

by Fused Contacts as the Sil-O2-Flex lens. JTX-10 at col.8 line 23, col.8 line 38; JTX-12 at 238.

57. The Sil-O2-Flex lens had an oxygen permeability level of approximately 5 to 8

Dk. JTX-10 at col.8 line 38; JTX-12 at 238.

58. On September 22, 1978, a group of scientists led by Kyoichi Tanaka in Japan

applied for a patent based on a novel polymer to be used for making an RGP contact lens.

JTX-13 at [57].

59. Tanaka discloses that his copolymers have an excellent oxygen permeability and a

good hydrophilic property (i.e., they are wettable). Jan. 28 PM Tr. at 79:17-19 (Long).

60. Tanaka departed from Gaylord (and Ellis) in two ways. First, rather than using

the Tris monomer, Tanaka employed a novel non-Tris silicone monomer containing

siloxanylalkyl ester groups, which are hydrophobic, and internal glycerol or polyether groups,

which are hydrophilic. Tanaka’s novel monomer thus was “amphiphilic,” and had a higher

affinity for water – i.e., was less water repellant – than the Tris monomer used by Gaylord and

Ellis. Jan. 28 PM Tr. at 5:5-8, 5:13-14, 6:11-7:3, 9:14-21 (Long). Strands were then formed by

polymerizing this novel non-Tris monomer and MMA as comonomers. Jan. 28 PM Tr. at 5:3-8,

7:7-10 (Long); JTX-13 at col.7 lines 39-41.

61. Second, Tanaka proposed a variety of cross-linking agents, including some cross-

linkers that were not employed by Gaylord and Ellis. Although Tanaka stated that a cross-linker

17
used by Gaylord, ethylene glycol dimethacrylate, could be used in his polymer, JTX-13 at col.8

lines 2-14, Tanaka’s “preferred” cross-linking agents were multifunctional siloxanyl alkyl esters

having a siloxane bond (which he described as formula [IV] cross-linkers) and multifunctional

siloxanyl alkanol esters, also having a siloxane bond (formula [V] cross-linkers). JTX-13 at

col.8 lines 11-46; see also Jan. 28 PM Tr. at 77:25–78:22 (Long); JTX-16 at 5 (Board Finding

No. 26).

62. Tanaka says that these cross-linking agents are preferred because the siloxane

bonds provide increased oxygen permeability to the cross-linked copolymer:

Since these cross-linking agents of the general formulas [V] and
[VI] have siloxane bonds in their molecules, the oxygen
permeability of the obtained cross-linked copolymers is high and,
therefore, they are preferably employed in the present invention.

JTX-13 at col.8 lines 35-39; see Jan. 28 PM Tr. at 77:25–78:16 (Long); JTX-16 at 5-6 (Board

Finding 27).

63. Tanaka states that the novel siloxanyl alkynol esters of formula [V] are

“particularly useful” because they contain hydrophilic hydroxyl groups. That is, not only do

these cross-linkers promote a material’s oxygen permeability, but they also promote its

wettability. JTX-13 at col.8 lines 39-46.

64. The multifunctional siloxanyl alkyl esters referenced by Tanaka had been known

in the field of polymer chemistry since at least 1958, and had been disclosed in the Mercker

Patent, see PTX-1; Jan. 28 PM Tr. at 107:8-23 (Long), but there is no evidence that it had been

purposely employed in contact lens production prior to Tanaka. See Jan. 28 PM Tr. at 107:8–

108:6.

65. Tanaka’s patent was issued on November 25, 1980. JTX-13 at [45].

18
 b. The Neefe Invention

66. Beginning around 1977, Russell Neefe undertook to create a rigid gas permeable

material suitable for contact lenses. Jan. 29 PM Tr. at 6:18-22 (Neefe).

67. At some point between 1977 and 1980, Neefe had the idea to cross-link the

silicone-containing Tris monomer not with the cross-linkers used by Gaylord, Ellis, or Novicky,

but with a cross-linking agent based on Tris. Jan. 29 PM Tr. at 15:16-23 (Neefe). This type of

cross-linking agent – a multifunctional siloxanyl alkyl ester – was one of the agents preferred by

Tanaka. See FF. 61-62.8

68. The initial material created by Neefe using the process of claim 1 had a Dk value

of 14. Jan. 29 PM Tr. at 19:15-20:1 (Neefe).

69. On September 8, 1980, Russell Neefe submitted his application for the patent at

issue in this suit. A patent was issued to Neefe on December 15, 1981. JTX-1 at [45].

70. The Neefe Patent is entitled “Method of Making a Contact Lens Material With

Increased Oxygen Permeability.” JTX-1.

71. The Summary of Invention in the Neefe Patent specification states that the

“primary object of this invention is to provide a novel contact lens material which is prepared

from a combination of monomers so as to have high oxygen, carbon dioxide permeability, and a

hydrophilic surface.” JTX-1 at col.1 lines 61-64.

72. The Neefe Patent contains four claims, three of which were not subject to

reexamination because the PTO found no substantial question of patentability as to those claims.

JTX-34 at 1112.

8
Multifunctional siloxanyl alkyl esters (which can serve as cross-linking agents)
are distinct from monofunctional siloxanyl alkyl esters such as Tris (which cannot). See infra at
FF. 128 n.11.
19
 73. As noted supra at 3, claim 1 of the Neefe Patent outlines a six-step process for

making a rigid gas permeable contact lens material, labeled (a) through (f). JTX-1 at col.5 lines

38-64.

74. The first five steps of the claim (steps (a)-(e)) recite a process of making 1,1,1-

tris(trimethylsiloxy)methacryloxypropylsilane, or “Tris.” JTX-1 at col.5 lines 44-54; JTX-16 at

2 (Board Findings 4-6); Jan. 28 AM Tr. at 69:1-70:5 (Long). There is no dispute that Tris was

known in the prior art. Director’s PFF. 34; Dome’s Resp. PFF. 34.

75. Step (f) of the claim instructs that four chemical ingredients, including Tris, are

combined to form “an oxygen permeable contact lens material.” JTX-1 at col.5 lines 55-64.

76. The four ingredients combined in step (f) are as follows: (1) “from 5% to 90% by

weight” of the Tris monomer; (2) from “3% to 90% by weight of an ester of acrylic or

methacrylic acid;” (3) “from 0.5% to 90% by weight of a surface wetting agent;” and (4) “from

0.01% to 90% by weight of an oxygen permeable crosslinking agent selected from the class of

multifunctional siloxanyl alkyl esters.” JTX-1 at col.5 lines 55-64; id., Certificate of Correction.

77. The first three ingredients listed in step (f) of claim 1 of the Neefe patent were

previously disclosed by Gaylord. The only significant difference between the contact lens

material taught by Gaylord and the contact lens material in claim 1 of the Neefe Patent is the

fourth ingredient: Gaylord’s material includes a hydrophilic cross-linking agent rather than the

hydrophobic multifunctional siloxanyl alkyl ester used by Neefe. JTX-8 at col.6 lines 3-12;

JTX-1 at col.2 lines 43-44 at col.5 lines 61-63; Jan. 28 PM Tr. at 16:3-5, 16:12-13, 17:4-10, 18:2,

70:15-20 (Long).

20
 78. As noted supra at FF. 61-63, Tanaka suggested the use of a siloxanyl alkyl ester

cross-linker in order to promote oxygen permeability, although Tanaka suggested its use with a

different (non-Tris) monomer.

79. Four years later, Neefe created another material using the process of claim 1 of

the Neefe Patent, which was commercialized and sold under the trade name TransAire. Jan. 30

AM Tr. at 79:25–80:4, 83:3-5 (Neefe). The TransAire polymer had a Dk value of 45. Jan. 30

AM Tr. at 81:15-18 (Neefe); JTX-27 at 273.

c. An Artisan of Ordinary Skill Would Have Known That Tris Monomer and a Siloxanyl Alkyl
Ester Cross-Linker (like Tris Dimer or Trimer) Could Be Combined to Form an Oxygen
Permeable Polymer

80. A person of ordinary skill in the art of making RGP contact lens materials, as of

September 8, 1980, would have had at least an undergraduate degree – and very likely a graduate

degree or some graduate training – in chemistry, coupled with experience in the development,

manufacture and use of polymers suitable for the manufacture of RGP contact lenses. Jan. 28

PM Tr. at 60:15-19 (Long).

81. The person having ordinary skill in the art was aware of the reasons for and

desirability of high oxygen permeability in contact lens materials. JTX-16 at 8 (Board Finding

50); see Director’s PFF. 46; Dome’s Resp. PFF. 46.

82. A person of ordinary skill in the art would have fully understood the

copolymerization chemistry used to make contact lens materials, including the mechanism

involved in cross-linking different comonomers. JTX-16 at 8:10-23; see Director’s PFF. 47;

Dome’s Resp. PFF. 47; Dome’s PFF. 69; Director’s Resp. PFF. at 3, 5-6.

83. The person having ordinary skill in the art also would have understood and been

familiar with the processes and chemistry for making the comonomers that are copolymerized in

21
making contact lens materials. JTX-16 at 8 (Board Finding 53); see Director’s PFF. 49; Dome’s

Resp. PFF. 49.

84. One having ordinary skill in the art would have been familiar with the properties

of Tris and the chemistry necessary to make it. JTX-16 at 8 (Board Finding 54); see Director’s

PFF. 50; Dome’s Resp. PFF. 50.

85. One having ordinary skill in the art would have understood that cross-linking

takes place through terminal unsaturated carbon bonds. JTX-16 at 8, 16; see Director’s PFF. 48,

84; Dome’s Resp. PFF. 48, 84.

86. One having ordinary skill in the art would have understood that ethylene glycol

dimethacrylate, described as a cross-linker by both Gaylord and Tanaka, may be represented by

the following formula showing terminal unsaturated carbons (=CH2):

One having ordinary skill in the art would have understood that Tanaka’s preferred oxygen

permeable cross-linkers similarly have terminal unsaturated carbons (=CH2). For example, the

multifunctional siloxanyl alkyl esters employed by Tanaka include those represented by the

following general formula:

22
JTX-16 at 15 n.5; Director’s PFF. 83; Dome’s Resp. PFF. 83.

87. A person of ordinary skill in the art would have expected that these

multifunctional siloxanyl alkyl ester cross-linking agents, having terminal unsaturated carbons

(=CH2), would be effective cross-linking agents with the comonomers suggested by Gaylord.

See JTX-16 at 16.

88. The person having ordinary skill in the art would have recognized that the oxygen

permeability of Tanaka’s lens material was due in part to the use of Tanaka’s preferred cross-

linking agents, which contain siloxane bonds. See JTX-13 at col.8 lines 35-39; Jan. 28 PM Tr. at

79:15-16 (Long); see also JTX-16 at 6, 14.

89. A person of ordinary skill in the art would reasonably expect that combining the

comonomers suggested by Gaylord and the multifunctional siloxanyl alkyl ester cross-linking

agent suggested by Tanaka would likely yield positive results in terms of oxygen permeability.

See JTX-16 at 6 (Board Finding 28); Director’s PFF. 78-86; Dome’s Resp. PFF. 78-86 (asserting

that an artisan of ordinary skill would have been deterred from combining Gaylord’s and

Tanaka’s compounds for other reasons, but not disputing that such artisan would know that these

materials could be combined to promote oxygen permeability); Dome’s Trial Brief at 4 (“It was

known that incorporating a type of chemical called a ‘silicone’ (of which Tris is an example) in

the contact lens material would improve its oxygen permeability.”).

23
 C. A Person of Ordinary Skill in the Art Would Not Be Deterred, Because of Concern about
Wettability or Opacity, from Using the Siloxanyl Alkyl Ester Monomor Suggested by Gaylord
(Tris) with the Siloxanyl Alkyl Ester Cross-Linker Suggested by Tanaka

As noted, a person of ordinary skill in the art would have known that the

multifunctional siloxanyl alkyl ester cross-linking agent referenced by Tanaka could be used

with the Tris monomer, and that such combination would promote oxygen permeability. See FF.

89. Nevertheless, Dome maintains that the artisan of ordinary skill would have been dissuaded

from using these materials together, due to the hydrophobic properties of both. See Jan. 30 PM

Tr. at 8:2–9:18, 10:6-20 (Dome closing argument). The Director disagrees, arguing that the

artisan of ordinary skill would know that she could offset the hydrophobicity of the two

compounds by adding hydrophilic comonomers within the broad ranges identified by Neefe.

Jan. 30 PM Tr. at 17:2-7; 18:14–20:6 (Director closing argument).

Upon consideration of the entire record, the Court finds as follows:

90. A person of ordinary skill in the art at the time of the invention would understand

that any candidate material for making RGP contact lenses must simultaneously achieve design

goals that are often in tension with one another. Jan. 28 PM Tr. at 61:5-10 (Long).

91. Tanaka teaches that polymers “consisting essentially of” a siloxanyl alkyl ester

(such as Tris) and having no hydrophilic groups have very strong water repelling properties and

therefore are unsuitable for contact lenses. JTX-13 at col.3 lines 10-23.

92. Tanaka teaches that the water repelling nature of polysiloxanyl alkyl ester

monomers can be repressed by reducing the number of hydrophobic alkylsiloxy groups in the

polymer. Such reduction, however, will lead to a reduction in oxygen permeability:

In case of such a polysiloxanylalkyl ester monomer, when the
water repelling property is repressed by reducing the number of the
alkylsiloxy groups in the obtained polymer, the oxygen
permeability becomes low, and then the oxygen permeability is

24
 raised by increasing the number of the alkylsiloxy groups in the
obtained polymer, the water repelling property becomes strong. In
any case, there cannot be obtained a polymer suited for preparing a
contact lens which can be comfortably worn continuously for a
long period of time.

JTX-13 at col.3 lines 41-51; see also Jan. 28 PM Tr. at 8:13–9:8 (Long).

93. Tanaka also warns that a polysiloxanyl alkyl ester monomer such as Tris could

become opaque when combined with hydrophilic monomers.

[T]he polysiloxanylalkyl ester monomer may be copolymerized
with a hydrophilic monomer to provide the obtained copolymer
with a proper hydrophilic property, but since it is hard to
copolymerize with the hydrophilic monomer, the copolymer is
liable to become opaque. This is a fatal defect for use as contact
lens materials. Therefore, the polymerization ratio of the
hydrophilic monomer to the polysiloxanylalkyl ester monomer is
limited to produce a transparent copolymer, and it is very difficult
to decrease the water repelling property by copolymerizing with a
hydrophilic monomer.

JTX-13 at col.3 lines 23-41.

94. Tanaka sought to create a continuous wear lens (i.e., an extended or overnight

wear lens), not a daily wear lens or a prolonged daily wear lens. JTX-13, Abstract (describing

invention as contact lenses that “can be comfortably worn continuously for a long period of

time”); id. at col.1 lines 9-10; id. at col.1 lines 31-32; id. at col.3 lines 50-51; id. at col.3 lines

60-63; id. at col.11 lines 4-5; id. at col.11 lines 13-14; id. at col.11 lines 50-52; id. at col.27 lines

43-65 (noting that Tanaka contact lenses “were worn on rabbit eyes continuously for 21 days,”

and “could be continuously worn without change in eyes”).9

9
Dome disputes the Director’s assertion that Tanaka sought to create a continuous
or extended wear lens, noting that Tanaka never used the phrase “continuous wear” or “extended
wear” in his patent. See Dome’s Resp. PFF. 103. After reviewing the record, however, and in
particular the patent specification language cited above at FF. 94, the Court agrees that Tanaka’s
invention is directed towards a continuous wear lens.
25
 95. “Continuous wear” is a term that is analogous to “extended wear,” where the

individual continues to wear the same lens without interruption for several days, even while

sleeping. Jan. 30 AM Tr. at 10:20–11:1 (Benjamin); see also Jan. 29 AM Tr. at 28:10-12

(Melamed).

96. The oxygen permeability of a contact lens worn in extended wear or continuous

wear needs to be much greater than the oxygen permeability of a lens to be worn for daily wear.

Jan. 30 AM Tr. at 21:20-24 (Benjamin).

97. Although Tanaka warned that it could be difficult to increase a Tris-based

polymer’s wettability simply by adding hydrophilic monomers, prior references in the art taught

that hydrophilic monomers could be used, within limits, to offset hydrophobic monomers such as

Tris.

98. For example, Gaylord discloses that other ingredients can be added to a siloxanyl

alkyl ester to materially affect the basic properties of a contact lens material. Specifically,

Gaylord discloses using from 30 to 90 parts by weight acrylic or methacrylic acid ester, JTX-8 at

col.4 lines 14-16, both of which are hydrophilic. Jan. 28 PM Tr. at 64:11-19 (Long).

99. Gaylord also explains that, even if the resulting contact lens material is not

sufficiently wettable on its own, “several alternate methods” can be used “to improve the

wettability of” contact lenses. JTX-8 at col.5 lines 39-58.

100. For example, “wettability can be imparted to the copolymer by the addition of

from about 0.1% to about 10% by weight of one or more hydrophilic monomers.” JTX-8 at col.5

lines 42-45.

101. Gaylord also states that “the wettability of the surface of contact lenses made

from the copolymers can be improved by the application of a wetting agent[,] . . . by exposure of

26
the surface to a corona discharge or by chemical treatment of the surface with a strong oxidizing

agent such as nitric acid.” JTX-8 at col.5 lines 51-58.

102. Gaylord further describes that those methods are effective at yielding a wettable

material – a lens made with 55 parts Tris (which is hydrophobic), 45 parts methyl methacrylate

(which is hydrophilic), and 2 parts methacrylic acid (which is a hydrophilic wetting agent) “is

readily wetted with a wetting agent solution.” JTX-8 at col.8 lines 5-19.

103. Gaylord also states that these materials will yield a “transparent” material, JTX-8

at col.8 lines 5-22, and thus Gaylord teaches that Tris can be copolymerized with hydrophilic

monomers like MMA and surface wetting agents without making the copolymer opaque.

104. In addition, Gaylord teaches that a material can contain relatively high amounts of

hydrophobic monomers and still be wettable. For example, Gaylord discloses that lenses with as

much as 70 parts by weight of Tris are wettable, even though Tris is hydrophobic. See JTX-8,

Abstract; id. at col.1 lines 17-18; id. at col.12 line 50 (claiming material that is up to 70 parts by

weight of Tris); id. at col.7 line 21 (disclosing material of 55 parts Tris); id. at col.7 line 38

(disclosing material of 60 parts Tris).

105. Claim 1 of the Neefe Patent permits as little as 0.01% of the hydrophobic cross-

linking agent, along with 5% of Tris, which is hydrophobic, so it permits as much as 94.99% of

hydrophilic comonomers. JTX-1 at col.5 lines 55-64. The prior art does not teach that a material

composed 5% of Tris, .01% of a hydrophobic cross-linking agent, and 94.99% of hydrophilic

comonomers would be unwettable. See FF. 102, 104.

106. Dr. Long states that as of September 8, 1980, a person of ordinary skill in the art

would not have reasonably expected that the siloxanyl alkyl ester cross-linker preferred by

Tanaka could be used with a Tris-based polymer in order to create a contact lens. See Jan. 28

27
PM Tr. at 108:1-6. But this conclusion is not consistent with other evidence presented at trial.

See FF. 90-105.

107. Dr. Long testified that he did not know what continuous wear or extended wear

lenses are, and that such knowledge was beyond the scope of his synthetic polymer chemistry

skills. Jan. 28 PM Tr. at 81:14-21 (Long). This lack of knowledge may have affected and

limited Dr. Long’s understanding of Tanaka and his teachings.

108. In light of Findings of Fact 90 through 107, the Court finds that even if the

Tanaka patent “teaches away” from the use of hydrophobic compounds such as Tris, it only

discourages using such compounds when seeking to make a material that “can be comfortably

worn continuously for a long period of time.” It did not teach away from using such compounds

for daily wear or prolonged daily wear.

109. In light of Findings of Fact 90 through 108, the Court finds that a person of

ordinary skill in the art would not be deterred, out of concerns about wettability or opacity, from

using the Tris monomer suggested by Gaylord along with the siloxanyl alkyl ester cross-linker

preferred by Tanaka to create a daily wear or prolonged daily wear contact lens, provided that

other, hydrophilic comonomers also were employed.

D. Dome’s Evidence of Secondary Considerations

Dome argues that the process recited in claim 1 of the Neefe Patent satisfied a

long-felt need for a contact lens that could be worn throughout the entire day. Dome notes that a

variety of first generation lenses (such as Polycon II and Boston II) based on prior art could not

be comfortably worn from when the wearer woke up in the morning until she went to bed in the

evening. By contrast, the Boston IV lens, a second generation lens that Dome contends

embodies claim 1 of the Neefe Patent, could be worn without interruption from morning until

28
evening. The Boston IV lens achieved considerable commercial success as compared to its

predecessor, the Boston II lens, which Dome asserts was not manufactured in accordance with

claim 1. Dome argues that the positive results achieved in the Boston IV lens and the ensuing

commercial success provides objective evidence of the nonobviousness of claim 1. See Jan. 30

PM Tr. at 12:6–13:10.

The Director maintains that many of the assumptions underlying Dome’s

arguments are flawed. To begin with, the Director takes issues with Dome’s assertion that the

Boston IV lens embodies claim 1 of the Neefe Patent, since the Boston IV process does not

strictly comply with the sequence of steps for making Tris as specified in claim 1. Therefore,

according the Director, the popularity of Boston IV cannot be used to shed light on the novelty of

claim 1. The Director next argues that the success of the Boston IV lens was attributable to a

number of factors, only one of which possibly relates to the Neefe Patent. Finally, the Director

contends that the positive, commercially desirable properties of the Boston IV lens are unlikely

to be present in other embodiments falling within the claim’s broad range. Thus, even if the

success of the Boston IV lens suggests that the process for the Boston IV lens was not obvious,

the evidence is irrelevant to the obviousness of other processes falling within the range of claim

1.

The parties’ disagreements turn both on questions of law and questions of fact.

The factual disputes center on how a person of ordinary skill in the art would interpret the

language of claim 1 of the Neefe Patent; whether a person of ordinary skill in the art would view

certain steps in the Boston IV and Boston II processes as equivalent to steps specified in claim 1;

and the reasons for Boston IV’s success. Upon consideration of the entire record, the Court finds

as follows:

29
 a. The Boston II and Boston IV Lenses
110. As noted supra at FF. 47-48, on May 1, 1979, a patent was issued for the

invention of Edward J. Ellis and his colleague, working at the Polymer Technology Corporation

(“PTC”), which is owned by Bausch & Lomb. JTX-9 at [54], [75], [45], [73].

111. Similar to the Gaylord polymer, the Ellis polymer used the hydrophobic Tris

monomer, a hydrophilic MMA monomer, a hydrophilic methacrylic acid as a wetting agent, and

traditional, hydrophilic cross-linking agents. Jan. 28 AM Tr. at 73:25–74:2 (Long); 75:1-11;

JTX-9 at col.3 line 68, col.4 lines 24-27, col.5 line 4, col.10 lines 28-33.

112. The Ellis polymer differed from the Gaylord polymer, however, in that Ellis

added an additional hydrophilic monomer called itaconate in order to improve the stability and

the wettability of the polymer. Jan. 28 AM Tr. at 73:10-16, 74:2-14 (Long); JTX-4 at 64; JTX-9

col.10 lines 28-33.

113. Contact lenses incorporating the Ellis polymer were introduced into the

marketplace in 1983 by PTC as the Boston II lens. JTX-10 at col.2 lines 48-51; PTX-3 at

BL5513; see also JTX-4 at 64, 66.

114. A year later, in 1984, PTC introduced the Boston IV lens as part of a “second

generation” of RGP contact lenses. Jan. 29 AM Tr. at 23:12-15, 55:5-7 (Melamed); Jan. 29 AM

Tr. at 43:16–44:22.

115. Both the Boston II contact lens and the Boston IV contact lens are made from an

oxygen permeable material formed by a process that includes the copolymerization of Tris by

procedures specified in Bausch & Lomb manufacturing protocols. JTX-21 at BL8556-57. Both

procedures begin with the synthesis of TX-91, a specific formulation of Tris. Jan. 28 PM Tr. at

56:4-7 (Long); JTX-17 at BL31.

30
 116. As discussed in FF. 117 to FF. 129, the five step process used to formulate TX-91

corresponds to steps (a) through (e) of the Neefe Patent.10

b. Formulation of TX-91

117. First, the production of TX-91, a specific formulation of Tris, begins by mixing

600 mL methacryloxypropyltrimethoxysilane (“MPS”) and 1200 mL trimethylchlorosilane

(“TMCS”), for a molar ratio of TMCS to MPS of 3.75 to 1, in a 3 liter round bottom flask. JTX-

18 at BL3, Step 7.1.2.

118. This process is performed in the exact manner as set forth in step (a) of claim 1 of

the Neefe Patent. Jan. 28 PM Tr. at 27:20-28:2 (Long); JTX-1 at col.5 lines 38-64.

119. Second, the mixture of MPS and TMCS is added to one-third volume of water and

cooled with an external ice/water bath. JTX-18 at BL4, step 7.1.3-7.1.4.

120. This combined use of one-third volume of water (which catalyzes the hydrolysis

reaction) and an external ice/water bath (which acts as a heat sink to absorb the excess heat

produced in the exothermic reaction) is not performed in the exact manner as any step recited in

the Neefe Patent. See JTX-1 at col.5 lines 38-64. This combined use performs substantially the

same functions, however, as the 3 to 10-fold excess volume of water recited in step (b) of claim 1

of the Neefe Patent (i.e., catalyzing the hydrolysis reaction and absorbing excess heat), in

substantially the same way (i.e., by providing the water needed for incorporation during the

chemical reaction and serving as a heat buffer), to achieve substantially the same result (i.e.,

forming Tris and limiting the formation of undesired by-products that can form under conditions

10
The parties introduced no evidence at trial suggesting that the Boston II or the
Boston IV processes were intentionally based on the Neefe Patent.
31
of excessive heat). JTX-18 at BL4, step 7.1.3-7.1.4; Jan. 28 PM Tr. at 33:16-34:20 (Long); see

also JTX-6 at col.1 lines 52-54.

121. Third, the mixture of MPS, TMCS, and water is stirred slowly for 12 to 16 hours.

Jan. 28 PM Tr. at 36:1-14 (Long); JTX-18 at BL4, Step 7.1.5.

122. This process is performed in the exact manner as set forth in step (c) of claim 1 of

the Neefe Patent. Jan. 28 PM Tr. at 36:21-37:1 (Long); JTX-1 at col.5 lines 38-64.

123. Fourth, the mixture of MPS, TMCS, and water is transferred to a separatory

funnel, allowed to separate, and the upper organic layer is retained. Jan. 28 PM Tr. at 37:21-25,

38:1-5 (Long); JTX-18 at BL4, Step 7.1.6.

124. Fifth, volatiles (including the unwanted by-product hexamethyldisiloxane) are

then removed under vacuum using a rotary evaporator or its equivalent. Jan. 28 PM Tr. at

39:17–40:1 (Long); JTX-18 at BL4, Step 7.1.9. The mixture is then filtered. Jan. 28 PM Tr. at

38:9-17 (Long); JTX-18 at BL5, Step 7.2.2. See generally JX-18.

125. The separation step and the vacuum distillation and filtration steps correspond to

steps (d) and (e) of claim 1 of the Neefe Patent. The order in which each action is performed,

however, differs from the sequence described in claim 1, which requires that the upper organic

layer of the mixture is “remove[d] and filter[ed]” in step (d), and that the hexamethyldisiloxane

“is then removed by vacuum distillation” in step (e). JTX-1 at col.5 lines 51-54 (emphasis

added).

126. Nevertheless, a person of ordinary skill in the art would view filtration followed

by vacuuming as equivalent to vacuuming followed by filtration. Jan. 28 PM Tr. at 40:12-15,

54:23-25, 87:8-9, 94:14-15 (Long). The Court bases this finding on the following facts:

32
 a. Both the filtration process and the vacuum distillation process are used to purify

the desired Tris by removing unwanted materials. Jan. 28 PM Tr. at 54:7-14

(Long).

b. Dr. Long testified that the presence of insoluble impurities or by-products will not

alter the way in which the vacuum distillation process works, or its effectiveness

in removing soluble materials. Jan. 28 PM Tr. at 54:7-14, 54:23-25 (Long). He

also testified that the presence of unwanted soluble, organic impurities or

byproducts will not alter the way in which the filtration process works, or its

effectiveness in removing particulate materials. Jan. 28 PM Tr. at 54:7-14,

54:23-25 (Long).

c. No evidence was presented at trial indicating that the effectiveness of the filtration

process depends on whether the filtration occurs before or after vacuum

distillation; nor was any evidence presented that the effectiveness of the vacuum

distillation process depends on whether distillation occurs before or after

filtration.

127. After the five steps described above are completed, the resulting solution is

TX-91. TX-91 consists of at least 85% Tris monomer; the remaining percentage is Tris dimer or

trimer. JTX-17 at BL 31; Jan. 28 PM Tr. at 23:8-16 (Long).

128. Tris dimer and Tris trimer are both in the class of multifunctional siloxanyl alkyl

esters required for step (f) of claim 1 of the Neefe Patent. Jan. 28 PM Tr. at 58:6–59:1 (Long).11

11
Although the parties did not introduce extensive evidence at trial about the nature
of Tris dimer and trimer, they appear to agree that the term multifunctional signifies that the
monomer has two or more ends that can react and join with other comonomers. It is this
property that enables a multifunctional compound – such as Tris dimer (two ends) or trimer
(three ends) – to serve as a cross-linking agent. By contrast, a Tris monomer (one end) can be
33
 129. TX-91 is the first ingredient used in both the Boston II manufacturing process and

the Boston IV process. See generally JX-18; Jan. 28 PM Tr. at 56:4-13 (Long); Jan. 28 PM Tr.

at 56:4-7 (Long). From this point, however, the Boston II process and the Boston IV process

diverge.

c. The Boston II Lens

130. As noted, the first compound used in the Boston II copolymerization process is

TX-91. Jan. 28 PM Tr. at 56:4-13 (Long).

131. TX-91, as prepared in steps (a) through (e) above, comprises approximately

41.7% by weight of the Boston II copolymer. JTX-17 at BL24, BL31. The main component of

TX-91, the Tris monomer, therefore comprises 35.5% to 41.7% by weight of the Boston II

copolymer. Jan. 28 PM Tr. at 56:14-15 (Long); JTX-17 at BL24, BL31.

132. This percentage of Tris falls within the range specified for this reactant in step (f)

of claim 1 of the Neefe Patent. Jan. 28 PM Tr. at 56:18–57:1 (Long); JTX-1 at col.5 lines 38-64.

133. The second comonomer used in the copolymerization process is an ester of acrylic

or methacrylic acid. Jan. 28 PM Tr. at 57:2-8 (Long).

134. An ester of acrylic or methacrylic acid comprises 21.8% by weight of the

copolymer. JTX-17 at BL24, BL31.

135. This percentage of an ester of acrylic or methacrylic acid falls within the range

specified for this reactant in step (f) of claim 1 of the Neefe Patent. Jan. 28 PM Tr. at 57:2-12

(Long); JTX-1 at col.5 lines 38-64.

cross-linked, but it cannot itself serve as a cross-linker. See Jan. 30 PM Tr. 5:14-18 (Dome
closing arg.); Director’s Trial Brief at 10.
34
 136. The third class of comonomers used in the copolymerization process are the

surface wetting agents tetraethyleneglycol dimethacrylate (“CL”) and N-Nvinylpyrrolidone

(“NVP”). Jan. 28 PM Tr. at 58:1-3 (Long).

137. Together, these surface wetting agents comprise 9.9% by weight of the

copolymer. JTX-17 at BL24, BL31 (CL is 8.4% by weight; NVP is 1.5% by weight).

138. This percentage of surface wetting agents falls within the range specified for this

reactant in step (f) of claim 1 of the Neefe Patent. Jan. 28 PM Tr. at 58:1-5 (Long); JTX-1 at

col.5 lines 38-64.

139. No additional multifunctional siloxanyl alkyl esters are added to this mixture for

the Boston II process. JTX-17 at BL 24, 31.12

140. Multifunctional siloxanyl alkyl esters nevertheless are often present in the mixture

used to create the Boston II lens. This is because, as noted supra at FF. 127-128, TX-91 consists

of up to 15% Tris dimer or trimer, each of which is an example of the multifunctional siloxanyl

alkyl ester called for in step (f) of claim 1. JTX-17 at BL 31; Jan. 28 PM Tr. at 23:8-16,

24:19-23, 98:18–99:3 (Long).

141. Neefe himself disclosed embodiments using Tris dimer or trimer as the cross-

linking agent. Examples II and IV in the Neefe Patent specification employ a dimer of Tris. Jan.

28 PM Tr. at 17:24-18:2, 19:1-5 (Long); see also JTX-1 at col.3 lines 30-40, 62. Example VI of

the Neefe Patent employs a trimer of Tris. JTX-1 at col.4 lines 36-37.

142. Because TX-91 makes up 41.7% of the Boston II lens by weight (JTX-17 at BL

24; Jan. 28 PM Tr. at 56:10-11 (Long)), the Boston II lens can be comprised up to 6.2% by

12
Other compounds were present in the Boston II lens as well, including dimethyl
itaconate. See JTX-17 at 24, 31.

35
weight of Tris dimer and trimer (i.e., 41.7% (percentage of TX-91 in the lens) multiplied by 15%

(maximum percentage of Tris dimer and trimer in TX-91)). See Director’s PFF. 149; Dome

Resp. PFF. 149.

143. PTC sought to minimize the presence of dimers and trimers in at least one of its

formulations of Tris. JTX-19 at BL 68, 70. There is no evidence, however, that the amount of

Tris dimer or trimer was minimized below .01% by weight. In fact, PTC calculated that the

Boston II lens contained approximately 1.3 mole percent of Tris dimer and trimer. JTX-21 at

8557, 8577.13

144. If Tris dimer and trimer are present in TX-91, then they will be cross-linked in the

copolymer. Jan. 28 PM Tr. at 97:18–98:6 (Long).

145. As noted supra at FF. 76, step (f) of claim 1 of the Neefe Patent requires that at

least .01% of the hydrophobic cross-linking agent – such as Tris dimer or Tris trimer – be

copolymerized with the Tris, the ester of acrylic or methacrylic acid, and the surface wetting

agent. JTX-1 at col.5 lines 55-64.

146. The maximum amount of Tris dimer and trimer permitted in the Boston II lens –

6.2% – falls well within the “0.01% to 90%” range of siloxanyl alkyl ester cross-linking agent

required in Step (f) of claim 1 of the Neefe Patent. See JTX-1 at col.5 lines 55-64.

147. The minimum amount of Tris dimer and Tris permitted in the Boston II lens – 0%

– falls narrowly outside of the “0.01% to 90%” range of siloxanyl alkyl ester cross-linking agent

required in Step (f) of claim 1 of the Neefe Patent. See id.

148. As noted supra at FF. 48, the oxygen permeability of the Boston II lenses

consistently was reported to be approximately 12 to 14 Dk. Jan. 29 AM Tr. at 25:22-25, 54:4-9

13
The parties have neither defined mole percent nor have they testified as to how to
convert mole percent to percent by weight for this copolymer.
36
(Melamed); Jan. 30 AM Tr. at 69:25-70:2, 75:21-25 (Benjamin); JTX-4 at 66 (12-14 Dk);

JTX-12 at 238 (12.6 Dk); JTX-21 at BL8556 (14.6 Dk); JTX-27 at 273 (12 Dk); PTX-2 at

BL4760 (14.6 Dk); but see JTX-20 at BL8328 (16.4 Dk).

d. The Boston IV Lens

149. Like the Boston II lens, the first compound employed in the Boston IV

copolymerization process is TX-91. Jan. 28 PM Tr. at 56:4-7 (Long); JTX-17 at BL31.

150. Sufficient amounts of TX-91 are used so that the Tris monomer comprises 38.3%

to 41.0% by weight of the copolymer. JTX-17 at BL31; Jan. 28 PM Tr. at 56:14-15 (Long).

151. This percentage of Tris monomer falls within the range specified in step (f) of

claim 1 of the Neefe Patent. Jan. 28 PM Tr. at 56:18–57:1 (Long).

152. As in the Boston II process, the second comonomer employed in the

copolymerization set forth in the Boston IV process is an ester of acrylic or methacrylic acid.

Jan. 28 PM Tr. at 57:2-8 (Long).

153. An ester of acrylic or methacrylic acid comprises 19.7% by weight of the

copolymer used for the Boston IV process. JTX-17 at BL24, BL31.

154. This amount of ester of acrylic or methacrylic acid falls within the range specified

in step (f) of claim 1 of the Neefe Patent. Jan. 28 PM Tr. at 57:2-12 (Long).

155. As in the Boston II process, the third class of comonomers employed in the

copolymerization set forth in the Boston IV process are the surface wetting agents tetraethylene

glycol dimethacrylate and N-Nvinylpyrrolidone. Jan. 28 PM Tr. at 58:1-3 (Long).

156. Together, these surface wetting agents comprise 8.1% by weight of the

copolymer. JTX-17 at BL24, BL31 (CL is 2.9% by weight; NVP is 5.5% by weight).

37
 157. This percentage of surface wetting agents falls within the range specified for this

reactant in step (f) of claim 1 of the Neefe Patent. Jan. 28 PM Tr. at 58:1-5 (Long).

158. Unlike in the Boston II process, in the Boston IV process TX-91 is modified to

become TX-82. TX-82 is prepared by adding substantial quantities of Tris dimer and Tris trimer

to the TX-91 formulation produced through steps (a) through (e), so as to increase the percentage

of Tris dimer to between 19.5 and 21 percent and Tris trimer to between 3 and 9.5 percent. Jan.

28 PM Tr. at 24:5-18, 58:20–59:1 (Long); JTX-17 at BL24, BL31; JTX-21 at BL8599-8603.

159. As noted supra at FF. 128, Tris dimer and trimer are each an “oxygen permeable

crosslinking agent selected from the class of multifunctional siloxanyl alkyl esters” as specified

in step (f) of claim 1 of the Neefe Patent. Jan. 28 PM Tr. at 58:6-24 (Long).

160. These percentages of Tris dimer and trimer fall within the range specified for this

reactant in step (f) of claim 1 of the Neefe Patent. Jan. 28 PM Tr. at 58:15-59:1, 59:25–60:7

(Long); JTX-1 at col.5 lines 38-64.

161. The reported oxygen permeability of the Boston IV lens was 19 to 28 Dk,

depending on the measurement technique used. Jan. 29 AM Tr. at 26:1-2, 56:1-4 (Melamed);

Jan. 30 AM Tr. at 37:24, 66:12-13 (Benjamin); JTX-4 at 66; JTX-21 at BL8556, BL8578;

JTX-22 at BL8739; JTX-23; JTX-27 at 273; PTX-2 at BL4760, BL4776; PTX-3 at BL5507.14

e. Boston II versus Boston IV

162. The only substantial difference between the Boston II and the Boston IV

manufacturing processes was that the Boston IV process involved the purposeful addition of Tris

dimer and trimer. One internal Bausch & Lomb document stated that the final concentration of

14
As with the Boston II lens, other compounds were present in the Boston IV lens,
including dimethyl itaconate. See JTX-17 at 24, 31.
38
Tris dimer and trimer in the Boston IV lens was 3.9 mole percent, three times that of the Boston

II lens (1.3 mole percent). JTX-21 at BL8557, BL8577.

163. There was at least a 50% increase in the oxygen permeability of the Boston IV

polymer over the Boston II polymer without impairment of wettability. Jan. 29 AM Tr. at

26:1-4, 62:11-13 (Melamed); JTX-4 at 66; PTX-3 at BL5513.

164. When calculating how much oxygen passes through an actual lens, one considers

its oxygen transmissibility, which takes into account the material’s thickness. Jan. 29 AM Tr. at

63:21-22 (Melamed); Jan. 30 AM Tr. at 23:18-19 (Benjamin); JTX-4 at 62.

165. Oxygen transmissibility is expressed as Dk/L, where Dk is the oxygen

permeability and L is the thickness of the given polymer. Jan. 29 AM Tr. at 65:11-14

(Melamed); JTX-4 at 62.

166. The Dk/L of a contact lens must be approximately 18 to 20 to prevent damage to

the cornea over the course of a prolonged wearing day. JTX-26 at 11.3 (“To produce virtually

no change in corneal thickness under daily wear conditions, a lens must provide an equivalent

oxygen percentage (EOP) of no less than 10%. Theoretically, this requires a Dk/L of

approximately 18-20.”). Jan. 29 AM Tr. at 91:13-21 (Melamed).

167. The oxygen transmissibility of the Boston IV lens is approximately 18.7 Dk/L,

and thus the lens is suitable for prolonged daily wear. JTX-4 at 206; Jan. 29 AM Tr. at 65:15-17,

76:7-20 (Melamed); JTX-26 at 11.3-11.4. By contrast, the oxygen transmissibility of the Boston

II lens is approximately 8.0 to 9.3 Dk/L, and thus the Boston II is not suitable for prolonged daily

wear. PTX-2 at BL4760; JTX-4 at 66, 206; Jan. 29 AM Tr. at 75:22-76:3 (Melamed); see also

Dome’s PFF. 291-96; Director’s Resp. PFF. at 14.

39
 168. The Boston IV lens was an improvement over the Boston II lens because of

increased oxygen permeability and oxygen transmissibility. Jan. 29 AM Tr. at 27:8-13

(Melamed).

169. The Boston IV lens largely displaced sales of the Boston II lens. Jan. 29 AM Tr.

at 45:7-16 (Melamed); PTX-3 at BL5513; JTX-31 at BL8309.

170. By 1988, the Boston IV lens commanded 65% of Bausch & Lomb’s total material

sales distribution, while the Boston II lens accounted for 10% of sales. JTX-31 at BL8309.

171. The Boston IV lens is still widely available today. Jan. 29 AM Tr. at 46:12-13

(Melamed); JTX-4 at 17.

172. Other factors in addition to increased oxygen permeability likely contributed to

the Boston IV lens’ commercial success: (i) patients could easily get a replacement lens for the

Boston IV lens because they were “consistent and readily reproducible” (Jan. 29 AM Tr. at

68:11-24 (Melamed)); (ii) patients were attracted to the Boston IV lens because it was durable

and lasted a long time (id. at 68:25 – 69:10 (Melamed)); (iii) the long-term costs of purchasing

the Boston IV lens were low for the consumer, so economics was an additional attractive feature

of the lens (id. at 71:3-12 (Melamed)); and (iv) Bausch & Lomb heavily promoted the Boston IV

lens, but not other lenses with higher oxygen permeability (e.g., the Boston Equalens lens) (id. at

80:8-23 (Melamed)).

f. Other Embodiments of Claim One of the Neefe Patent

173. The ranges identified in step (f) of the Neefe Patent are very broad. For example,

as noted supra at FF. 104, claim 1 of the Neefe patent permits as little as 0.01% of the

hydrophobic cross-linking agent, along with 5% of Tris, which is hydrophobic, so it permits as

much as 94.99% of hydrophilic comonomers. JTX-1 at col.5 lines 55-64.

40
 174. Dome did not introduce any expert evidence showing that a contact lens made

from ingredients in the amounts at the ends of those ranges would be sufficiently oxygen

permeable or wettable.

175. For example, Dome’s expert, Dr. Long, did not know whether a contact lens

material that is 5% by weight Tris monomer, 90% by weight MMA, 4.99% by weight surface

wetting agent, and 0.01% by weight a multifunctional siloxanyl alkyl ester would be sufficiently

oxygen permeable, even though such a lens material would fall within the scope of claim 1 of the

Neefe Patent. Jan. 28 PM Tr. at 86:7-23 (Long).

176. Nor did Dr. Long know whether a lens material that is 90% by weight Tris

monomer, 3% by weight MMA, 0.5% by weight surface wetting agent, and 6.5% by weight Tris

dimer as a cross-linker would be wettable, even though such a lens material would fall within the

scope of claim 1 of the Neefe patent. Jan. 28 PM Tr. at 85:20–86:6 (Long).

177. Based on the evidence introduced at trial regarding the Boston II lens, a person of

ordinary skill in the art would expect that a contact lens material comprised 35.5% to 41.7% by

weight of Tris monomer, 21.8% by weight of ester of acrylic or methacrylic acid, 9.9% by

weight of surface wetting agents tetraethyleneglycol dimethacrylate and N-Nvinylpyrrolidone,

and between .01% and 6.2% by weight of Tris dimer and trimer, and manufactured in accordance

with claim 1, would be wettable and would have an oxygen permeability of approximately 12 to

14 Dk. See FF. 131, 134, 137, 140, 142, 144, 148.

178. As noted supra at FF. 68, the initial material created by Neefe using the process

of claim 1 had a Dk value of 14. The parties did not introduce any evidence at trial about how

much of each ingredient (Tris monomer, MMA, surface wetting agent, and multifunctional

siloxanyl alkyl ester) was used in the manufacturing process of that material.

41
 179. As noted supra at FF. 79, the TransAire polymer, which was based on claim 1 of

the Neefe patent, had a Dk value of 45. The parties did not introduce any evidence at trial about

how much of each ingredient (Tris monomer, MMA, surface wetting agent, and multifunctional

siloxanyl alkyl ester) was used in the TransAire manufacturing process.

III. CONCLUSIONS OF LAW

A. Legal Standards

1. Burden of Proof

Once the PTO has determined that “a substantial new question of patentability” is

raised by a request for reexamination, the PTO initiates a reexamination proceeding. In re

Swanson, 540 F.3d 1368, 1375 (Fed. Cir. 2008) (quoting 35 U.S.C. § 303(a)). In a

reexamination proceeding, as in the initial examination of a patent application, the patent

examiner bears the initial burden of showing by a preponderance of the evidence that the

invention is unpatentable as obvious. See Rambus Inc. v. Rea, 731 F.3d 1248, 1255 (Fed. Cir.

2013) (“In reexamination proceedings, ‘a preponderance of the evidence must show

nonpatentability before the PTO may reject the claims of a patent application.’”) (internal

quotation omitted); In re Etter, 756 F.2d 852, 856 (Fed. Cir. 1985) (en banc). Once a prima facie

showing of obviousness is made, however, the burden shifts to the patent holder to demonstrate

nonobviousness. In re Giannelli, 739 F.3d 1375, 1379 (Fed. Cir. 2014); In re Glaug, 283 F.3d

1335, 1338 (Fed. Cir. 2002).

Dome objects to the application of this legal standard here, arguing that claim 1 of

the Neefe Patent may be cancelled only if the Director proves obviousness under a clear and

convincing evidence standard. In support of its position, Dome points to the standard of proof in

patent infringement proceedings initiated under 35 U.S.C. § 282. See Dome’s Prop. Concl. Law

42
11 (citing Microsoft Corp. v. i4i Limited Partnership, 131 S. Ct. 2238 (2011)). In Section 282

proceedings, a party accused of infringement may claim, as an affirmative defense, that the

relevant patent is invalid due to obviousness. To prevail on this defense, the accused infringer

must show obviousness by clear and convincing evidence. Section 282 is a fundamentally

different context than the present one, and the burdens of proof governing those proceedings are

inapplicable here. See In re Swanson, 540 F.3d at 1377 (noting that PTO examination and

reexamination proceedings “have distinctly different standards, parties, purposes, and outcomes”

than Section 282 infringement proceedings); In re Etter, 756 F.2d at 855-59; cf. Sciele Pharma

Inc. v. Lupin Ltd., 684 F.3d 1253, 1260 (Fed. Cir. 2012) (noting that the clear and convincing

standard applicable in Section 282 proceedings is rooted in a “necessary deference to the PTO”)

(internal quotation omitted).

The Court therefore considers whether the Director has shown by a

preponderance of the evidence that claim 1 of the Neefe Patent is prima facie obvious, and, if so,

whether Dome has rebutted this initial showing.

2. Standard of Review

A party subject to an adverse reexamination decision by the Board may seek

review of that decision in this Court under 35 U.S.C. § 145, or it may appeal the decision directly

to the Federal Circuit pursuant to 35 U.S.C. § 141.15 Unlike a Section 141 appeal, a Section 145

15
35 U.S.C. § 141 was amended on November 29, 1999, to provide the Federal
Circuit with exclusive jurisdiction of any challenge to the Board’s final decision in a
reexamination proceeding. 35 U.S.C. § 141; see generally Teles AG v. Kappos, 846 F. Supp. 2d
102, 111 (D.D.C. 2012). 35 U.S.C. § 145 was amended on September 16, 2011, changing the
venue for Section 145 actions from this Court to the United States District Court for the Eastern
District of Virginia. See Kappos v. Hyatt, 132 S. Ct. 1690, 1694 n.1 (2012). Neither amendment

43
proceeding in district court is a “unique ‘hybrid of an appeal and a trial de novo.’” Alberts v.

Kappos, 917 F. Supp. 2d 94, 104 (D.D.C. 2013), aff’d sub nom., Alberts v. Lee, 552 F. App’x

986 (Fed. Cir. 2014). In a Section 145 action, the parties may present new evidence that was not

presented to the PTO, and in so doing, are restricted only by the Federal Rules of Evidence and

the Federal Rules of Civil Procedure. Kappos v. Hyatt, 132 S. Ct. 1690, 1694 (2012). Where

new evidence is presented on a disputed question of fact, “[t]he district court must assess the

credibility of new witnesses and other evidence, determine how the new evidence comports with

the existing administrative record, and decide what weight the new evidence deserves.” Id. at

1700. The Court then “must make de novo factual findings that take account of both the new

evidence and the administrative record before the PTO.” Id. at 1701. Where no new evidence is

presented at all or with respect to certain facts found by the Board, the Court “must [instead]

apply the APA’s substantial evidence standard to Patent Office fact findings.” Hyatt v. Kappos,

625 F.3d 1320, 1336 (Fed. Cir. 2010) (en banc), aff’d, 132 S. Ct. 1690 (2012). Because new

evidence was presented on every significant, contested factual issue in this case, the Court’s

factual findings are largely de novo. Questions of law also are reviewed de novo. Cytologic,

Inc. v. Biopheresis GmbH, 682 F. Supp. 2d 1, 12 (D.D.C. 2010).

B. Analysis

1. The Director Has Made a Prima Facie Showing of Obviousness

“Whether a claim would have been obvious under 35 U.S.C. § 103(a) is a legal

conclusion based on underlying factual determinations.” Rambus Inc. v. Rea, 731 F.3d at

1251-52 (citing In re Kotzab, 217 F.3d 1365, 1369 (Fed. Cir. 2000)). These factual

is retroactive or applicable here, as the request for reexamination in this case was filed on August
27, 1998.

44
determinations “include (1) the scope and content of the prior art; (2) the differences between the

claims and the prior art; (3) the level of ordinary skill in the art; and (4) objective evidence of

nonobviousness.” Id. at 1251 (citing Graham v. John Deere Co. of Kansas City, 383 U.S. 1,

17-18 (1966)). The inquiry into obviousness “entails ‘an expansive and flexible approach.’”

Sciele Pharma Inc. v. Lupin Ltd., 684 F.3d at 1259 (quoting KSR Int’l Co. v. Teleflex Inc., 550

U.S. 398, 415 (2007)). If any embodiment within the scope of the claim is determined to be

obvious, then the entire claim is unpatentable for obviousness, regardless of whether other

embodiments are nonobvious. See ArcelorMittal France v. AK Steel Corp., 700 F.3d 1314, 1325

(Fed. Cir. 2012) (“‘[C]laims which are broad enough to read on obvious subject matter are

unpatentable even though they also read on nonobvious subject matter.’”) (quoting Muniauction,

Inc. v. Thomson Corp., 532 F.3d 1318, 1328 n.4 (Fed. Cir. 2008)).

It is undisputed that each of the compounds recited in claim 1 of the Neefe Patent

– the Tris monomer, the ester of acrylic or methacrylic acid, the surface wetting agent, and the

siloxanyl alkyl ester cross-linking agent – was known in the prior art. This fact alone, however,

does not establish obviousness. KSR Int’l Co. v. Teleflex Inc., 550 U.S. at 418-19 (“[A] patent

composed of several elements is not proved obvious merely by demonstrating that each of its

elements was, independently, known in the prior art.”); see also Stryker Spine v. Biedermann

Motech GmbH, 750 F. Supp. 2d 107, 122 (D.D.C. 2010). Where all of the elements of a claim

are known in the prior art, as is the case here, the obviousness inquiry generally will turn on two

factual questions:

(1) whether the prior art would have suggested to those of ordinary
skill in the art that they should make the claimed composition or
device, or carry out the claimed process; and

(2) whether the prior art would also have revealed that in so
making or carrying out, those of ordinary skill would have a
reasonable expectation of success.
45
Medichem, S.A. v. Rolabo, S.L., 437 F.3d 1157, 1164 (Fed. Cir. 2006) (quoting Velander v.

Garner, 348 F.3d 1359, 1363 (Fed. Cir. 2003)); see also In re Rosuvastatin Calcium Patent Litig.,

703 F.3d 511, 518 (Fed. Cir. 2012) (“[I]n cases involving new chemical compounds, it remains

necessary to identify some reason that would have led a chemist to modify a known compound in

a particular manner to establish prima facie obviousness of a new claimed compound.”) (internal

quotation marks omitted). A court “need not seek out precise teachings directed to the specific

subject matter of the challenged claim,” KSR Int’l Co. v. Teleflex Inc., 550 U.S. at 418, as the

analysis “can take account of the inferences and creative steps that a person of ordinary skill in

the art would employ.” Id.

In this case, the Director has demonstrated both the reason for combining the

compounds recited in claim 1 of the Neefe Patent and a reasonable expectation of success. A

person of ordinary skill in the art would have known that the ideal contact lens would have a

relatively high level of oxygen permeability, and would be motivated to combine comonomers

and cross-linkers to create an oxygen permeable polymer. See FF. 8-11, 81. This artisan also

would have known that the siloxanyl alkyl ester cross-linkers discussed by Tanaka promoted

oxygen permeability, as these cross-linkers contained a siloxane bond. FF. 61-62. And the

artisan would have known that the siloxanyl alkyl ester cross-linkers could effectively cross-link

the comonomers used by Gaylord and Ellis. FF. 80-88. It therefore would have been obvious to

a person of ordinary skill in the art that these materials, when combined with traditional

hydrophilic comonomers and wetting agents, could potentially be used to create an oxygen

permeable contact lens. FF. 89. The Director has established a prima facie case of obviousness,

and the burden shifts to Dome to prove nonobviousness.

46
 2. The Prior Art Does Not Teach Away from Combining the Elements in Claim 1 of the
Neefe Patent

A patentee may rebut a prima facie showing of obviousness by demonstrating that

the prior art “teaches away” from the claimed invention in any material respect. In re Peterson,

315 F.3d 1325, 1331 (Fed. Cir. 2003); see KSR Int’l Co. v. Teleflex Inc., 550 U.S. at 416

(“[W]hen the prior art teaches away from combining certain known elements, discovery of a

successful means of combining them is more likely to be nonobvious.”). Dome has taken this

tack, arguing that while it may have been apparent that both Tris monomer and siloxanyl alkyl

ester cross-linker promote oxygen permeability, the prior art “taught away” from attempting this

combination.

“A reference may be said to teach away when a person of ordinary skill, upon

reading the reference, would be discouraged from following the path set out in the reference, or

would be led in a direction divergent from the path that was taken by the applicant.” In re

Gurley, 27 F.3d 551, 553 (Fed. Cir. 1994) (collecting cases). The degree to which a reference

teaches away will depend on the particular facts, but the basic question is whether the reference

“suggests that the line of development flowing from the reference’s disclosure is unlikely to be

productive of the result sought by the applicant.” Id. “What a reference teaches and whether a

person of ordinary skill in the art would have been motivated to combine the teachings of

separate references are questions of fact.” Pregis Corp. v. Kappos, 700 F.3d 1348, 1353 (Fed.

Cir. 2012). When considering apparently conflicting references in the prior art, the fact-finder

must weigh each reference “for its power to suggest solutions to an artisan of ordinary skill . . .

consider[ing] the degree to which one reference might accurately discredit another.” Medichem,

S.A. v. Rolabo, S.L., 437 F.3d at 1165 (quoting In re Young, 927 F.2d 588, 591 (Fed. Cir.

1991)).

47
 As discussed above, see FF. 90-109, the prior references of Tanaka did not teach

away from combining Tris with a siloxanyl alkyl ester cross-linking agent, at least for daily wear

and prolonged daily wear lenses. Granted, Tanaka warned that in constructing a lens that “can

be comfortably worn continuously for a long period of time,” it was difficult, when using the

Tris monomer, to achieve high levels of oxygen permeability, clarity, and wettability, and that a

highly hydrophobic solution could not always be made wettable by simply adding high levels of

hydrophilic monomer – there were limits. FF. 91-94. But other references in the prior art taught

that Tris could be used effectively in the manufacturing of contact lenses, so long as hydrophilic

comonomers were used to offset the water-repellant properties of Tris. See, e.g., FF. 42, 97-104

(discussing Gaylord’s patent, which taught that Tris could be synthesized with hydrophilic

monomers like MMA and surface wetting agents without making the copolymer opaque);

FF. 47- 48 (discussing Ellis’s patent, which combined Tris and hydrophilic comonomers).16

Indeed, Tanaka himself recognized that the hydrophobic properties of Tris could be successfully

repressed – within limits – by the addition of hydrophilic compounds. To the extent that Tanaka

teaches away from using Tris altogether, the Court finds that such teaching can be fairly read as

confined to continuous wear lenses, see FF. 94, not to daily wear or prolonged daily wear lenses,

and that the teaching is outweighed by the teachings of Gaylord and Ellis.

16
Dome correctly points out that the Board twice suggested, erroneously, that a
multifunctional siloxanyl alkyl ester would be hydrophilic. See JTX-16 at 5:20-23 (describing
hydrophilic formula [V] as a multifunctional siloxanyl alkyl ester); id. at 16:6-8 (describing
hydrophobic “polyfunctional siloxanyl ester cross-linking agents” as hydrophilic). Dome argues
that this factual error infected the Board’s analysis. After reviewing the evidence presented to
the Board de novo, along with the evidence presented at trial, the Court is convinced that the
Board’s errors do not affect the correctness of the Board’s result.

48
 The Court therefore concludes that Dome has not rebutted the prima facie case of

obviousness by demonstrating that the prior art taught away from the method recited in claim 1.17

As the Board found, a person of ordinary skill in the art would have had a reasonable expectation

of success in combining the comonomers suggested by Gaylord and Ellis with the cross-linking

agents suggested by Tanaka.

3. Dome’s Evidence of Secondary Considerations Does Not Indicate Nonobviousness.

Dome also attempts to rebut the Director’s prima facie case using evidence of

secondary considerations, and in particular, evidence of commercial success. Secondary

considerations, “[s]uch as commercial success, long felt but unsolved needs, failure of others,

etc.,” often can “give light to the circumstances surrounding the origin of the subject matter

sought to be patented.” KSR Int’l Co. v. Teleflex Inc., 550 U.S. at 406 (quoting Graham v. John

Deere Co. of Kansas City, 383 U.S. at 17-18). Evidence that a patented invention attained

significant commercial success may provide an independent basis for inferring that the invention

was not obvious, “because the law presumes an idea would successfully have been brought to

market sooner, in response to market forces, had the idea been obvious to persons skilled in the

art.” Merck & Co., Inc. v. Teva Pharm. USA, Inc., 395 F.3d 1364, 1376 (Fed. Cir. 2005); see

also 3 MOY’S WALKER ON PATENTS § 9:62 (4th ed. 2013). Commercial success of an invention

over the prior art also implies that the difference between an invention and the prior art is

significant or substantial. 3 MOY’S WALKER ON PATENTS § 9:62. Although secondary

considerations must be taken into account, they do not necessarily control the obviousness
17
This question alternatively can be viewed as part of the inquiry into whether a
person of ordinary skill attempting the patented combination would have had a reasonable
expectation of success. Assuming arguendo that it is the Director’s burden of showing that
success would be reasonably expected despite the hydrophobicity of both the Tris monomer and
the siloxanyl alkyl ester cross-linking agent, the Court concludes that such burden has been
satisfied.
49
conclusion. Pfizer, Inc. v. Apotex, Inc., 480 F.3d 1348, 1372 (Fed. Cir. 2007) (citing Newell

Cos., Inc. v. Kenney Mfg. Co., 864 F.2d 757, 768 (Fed. Cir. 1988)); see Wyers v. Master Lock

Co., 616 F.3d 1231, 1246 (Fed. Cir. 2010) (“[S]econdary considerations of nonobviousness . . .

simply cannot overcome a strong prima facie case of obviousness.”).18

Dome asserts that an embodiment of claim 1 achieved unexpected results that led

to substantial commercial success. Dome also argues, with less force, that this embodiment

satisfied a long felt but unsolved need. See, e.g., Dome’s PFF. 351-402; Dome’s Prop. Concl.

Law at 36-40, 52; Dome Resp. Prop. Concl. Law 159, 194-95, 199, 229-30. The Director

contends that the evidence presented by Dome is irrelevant and unpersuasive.

a. Unexpected Results Leading to Commercial Success

Dome focuses on the commercial success of the Boston IV lens, which, according

to Dome, was manufactured using the process recited in claim 1 of the Neefe Patent. It is

undisputed that the Boston IV lens achieved significant commercial success over prior Bausch &

Lomb RGP lenses. See FF.169-71. But this success is only relevant to the obviousness inquiry

if Dome can establish the following: first, that the Boston IV lens embodies claim 1 of the Neefe

Patent – that is, that the lens is made in accordance with claim 1 of the Neefe Patent, see Brown

& Williamson Tobacco Corp. v. Philip Morris Inc., 229 F.3d 1120, 1130 (Fed. Cir. 2000);

second, that the success of the Boston IV lens was the result of the novel feature claimed in the

Neefe Patent, and not the result of some feature in the prior art, or some unrelated feature such as

increased marketing, see Tokai Corp. v. Easton Enterprises, Inc., 632 F.3d 1358, 1369 (Fed. Cir.

18
Secondary considerations are often referred to as objective evidence of
nonobviousness. See Demaco Corp. v. F. Von Langsdorff Licensing Ltd., 851 F.2d 1387, 1391
(Fed. Cir. 1988) (“The rationale for giving weight to the so-called “secondary considerations” is
that they provide objective evidence of how the patented device is viewed in the marketplace, by
those directly interested in the product.”).
50
2011); and third, that other embodiments of claim 1 could be expected to exhibit the same

commercially beneficial properties exhibited by the Boston IV lens, see MeadWestVaco Corp. v.

Rexam Beauty & Closures, Inc., 731 F.3d 1258, 1264-65 (Fed. Cir. 2013).

As discussed below, the Court agrees with Dome that there is a product – the

Boston IV lens – that embodies claim 1 of the Neefe Patent and that achieved some commercial

success. But the Court also finds that Dome has failed to present persuasive evidence that the

success of the Boston IV lens is the result of the novel feature claimed in the Neefe Patent, or

that other embodiments of claim 1 could be expected to exhibit the same commercially beneficial

properties as those possessed by the Boston IV lens. The Court discusses each of these points in

turn.19

i. The Boston IV lens Falls Within the Scope of Claim 1

Although neither Neefe nor Dome created the Boston IV lens, the success of this

product nevertheless may shed light on the obviousness (or nonobviousness) of Neefe’s

invention, so long as Dome shows that the Boston IV lens “embodies the claimed features” of

the patented invention – i.e., that it is made in accordance with claim 1 of the Neefe Patent.

Brown & Williamson Tobacco Corp. v. Philip Morris Inc., 229 F.3d at 1130.

As noted supra at FF. 149-159, the Boston IV lens is manufactured using the

following materials: 38.3% to 41.0% by weight of Tris; 19.7% of an ester of acrylic or

methacrylic acid; 8.1% of surface wetting agents (tetraethylene glycol dimethacrylate and

N-Nvinylpyrrolidone); and 19.5 to 21% and 3 to 9.5%, respectively, of Tris dimer and Tris
19
The Director moved to exclude testimony relating to the differences between the
Boston II and the Boston IV lens as irrelevant, based on a purported lack of nexus and
commensurateness. See Director’s Mot. in Limine to Exclude the Testimony of Dr. Melamed
and Portions of the Testimony of Dr. Long Pursuant to Rule 401 of the Federal Rules of
Evidence, Dkt. No. 66 (filed under seal, Dkt. No. 69) (Oct. 23, 2012). The Court declined to rule
on the motion at trial, but now will deny it.
51
trimer. These ranges fall within the ranges recited in claim 1 of the Neefe Patent, which calls for

from 5% to 90% by weight of Tris; from 3% to 90% of an ester of acrylic or methacrylic acid;

from .5% to 90% of a surface wetting agents; and from .01% to 90% of a siloxanyl alkyl ester

cross-linker, such as Tris dimer or trimer. See FF. 76. But as the Director points out, there are

two ways in which the synthesis of these compounds in the Boston IV lens process appears to

deviate from the process recited in claim 1.

First, as discussed in FF. 123-125, the manufacture of the Boston IV lens requires

that two steps – the vacuuming and the filtration of unwanted byproducts – occur in a different

order than the order recited in claim 1 of the Neefe Patent. Generally speaking, however, a claim

is not restricted to the performance of its steps in the order recited where sequence is not a clear

limitation in the claim, and where neither logic nor any aspect of the specification or prosecution

history requires a limiting construction. See Altiris, Inc. v. Symantec Corp., 318 F.3d 1363,

1370-71 (Fed. Cir. 2003); cf. Loral Fairchild Corp. v. Sony Corp., 181 F.3d 1313, 1322 (Fed.

Cir. 1999) (“Although not every process claim is limited to the performance of its steps in the

order written, the language of the claim, the specification and the prosecution history support a

limiting construction in this case.”). Although the ordering of the steps and the use of the word

“then” suggests an order, neither logic nor anything in the specification or prosecution history

suggests that the order of these steps would matter. See FF. 126. The Court therefore finds that

the vacuuming and filtering elements recited in claim 1 are literally present in the Boston IV

lens, and that the sequence of these steps is not a separate limitation of the claim. The variation

in sequence does not take the Boston IV lens outside the scope of claim 1.

Second, claim 1 of the Neefe Patent requires at step (b) that the mixture of

methacryl-oxypropyltrimethoxysilane and trimethylchlorosilane is added to water whose volume

52
is from 3 to 10 times that of the mixture. See JTX-1 at col.5 lines 38-64. By contrast, the

Boston IV manufacturing process calls for the addition of one-third volume of water to this

mixture of methacryloxypropyltrimethoxysilane and trimethylchlorosilane, followed by an

external ice/water bath. See FF. 119. Both parties agree that this step of the Boston IV process

is different from step (b) of claim 1; the water addition element of claim 1 thus is not literally

met by the Boston IV process. See Dome PFF. 308-11; Director’s Resp. PFF. 308-11. The

parties also agree that the addition of one-third volume of water in the Boston IV step, followed

by an ice/water bath, is substantially equivalent to claim 1’s step (b). See Dome PFF. 308-11;

Director’s Resp. PFF. 308-11. The Director asserts that this technical departure from the claim 1

process establishes that the Boston IV lens falls outside the scope of claim 1. Dome disagrees,

maintaining that the Boston IV lens falls within the scope of claim 1 under the doctrine of

equivalents, and therefore can inform the obviousness inquiry.

The doctrine of equivalents arose in the context of infringement disputes, and it

“grow[s] out of a legally implied term in each patent claim that ‘the claim extends to the thing

patented, however its form or proportions may be varied.’” Warner-Jenkinson Co., Inc. v. Hilton

Davis Chemical Co., 520 U.S. 17, 35 (1997); see also Festo Corp. v. Shoketsu Kinzoku Kogyo

Kabushiki Co., 535 U.S. 722, 733 (2002) (“The doctrine of equivalents allows the patentee to

claim those insubstantial alterations that were not captured in drafting the original patent claim

but which could be created through trivial changes.”). To evaluate whether a product or process

infringes under the doctrine of equivalents, the court asks “whether an asserted equivalent

represents an ‘insubstantial difference’ from the claimed element, or ‘whether the substitute

element matches the function, way, and result of the claimed element.’” Deere & Co. v. Bush

53
Hog, LLC, 703 F.3d 1349, 1356 (Fed. Cir. 2012) (quoting Warner-Jenkinson Co. v. Hilton Davis

Chemical, 520 U.S. at 40)).

Although neither party has pointed to any case directly addressing this question,

the Court is persuaded that the commercial success of a product that infringes a patent claim

under the doctrine of equivalents can inform whether the patent claim is obvious. To begin with,

the Director’s contention that a process that infringes by equivalence is outside the scope of a

claim is inconsistent with the established principle that “[t]he scope of a patent is not limited to

its literal terms but instead embraces all equivalents to the claims described.” Festo Corp. v.

Shoketsu Kinzoku Kogyo Kabushiki Co., 535 U.S. at 732. In this vein, courts have considered

the commercial success of a competitor’s infringing product or process as a secondary

consideration, without distinguishing between literal infringement or infringement by

equivalence. See, e.g., Brown & Williamson Tobacco Corp. v. Philip Morris Inc., 229 F.3d at

1130. Moreover, fact-finders in patent cases are instructed to take an “expansive and flexible

approach” when considering obviousness. KSR Int’l Co. v. Teleflex Inc., 550 U.S. at 415.

Where the differences between the process used to create a successful product and the process

claimed in the patent are insignificant, and where all evidence indicates that a product

manufactured in strict accordance with the claim language would be identical to the successful,

equivalent product, the commercial success of the equivalent product can shed light on the

patent’s obviousness. The Court therefore finds that the Boston IV lens falls within the scope of

claim 1 for purposes of the obviousness inquiry.

ii. Nexus Between Commercial Success and Claim 1

In order to rely on the commercial success of the Boston IV lens as evidence of

nonobviousness, Dome must show a legally and factually sufficient connection – a “nexus” –

54
between the merits of claim 1 of the Neefe Patent and the evidence of the Boston IV lens’

commercial success. Tokai Corp. v. Easton Enterprises, Inc., 632 F.3d at 1369; Wyers v. Master

Lock Co., 616 F.3d at 1246; Demaco Corp. v. F. Von Langsdorff Licensing Ltd., 851 F.2d 1387,

1392 (Fed. Cir. 1988). “A prima facie case of nexus is generally made out when the patentee

shows both that there is commercial success, and that the thing (product or method) that is

commercially successful is the invention disclosed and claimed in the patent.” Demaco Corp. v.

F. Von Langsdorff Licensing Ltd., 851 F.2d at 1392; see also Ormco Corp. v. Align Tech., Inc.,

463 F.3d 1299, 1312 (Fed. Cir. 2006) (“[W]hen a patentee can demonstrate commercial success,

usually shown by significant sales in a relevant market, and that the successful product is the

invention disclosed and claimed in the patent, it is presumed that the commercial success is due

to the patented invention.”) (internal quotation omitted); but see In re Huang, 100 F.3d 135, 140

(Fed. Cir. 1996) (requiring additional proof that increased sales “were a direct result of the

unique characteristics of the claimed invention”). Where the evidence shows that the

commercial success derived from some aspect of the prior art, or was the result of “economic

and commercial factors unrelated to the quality of the patented subject matter,” evidence of

commercial success will not be sufficient to demonstrate nonobviousness of a claimed invention.

In re DBC, 545 F.3d 1373, 1384 (Fed. Cir. 2008); see also Tokai Corp. v. Easton Enterprises,

Inc., 632 F.3d at 1369-70.

As discussed in the preceding subsection, the Boston IV lens falls within the

scope of claim 1 of the Neefe patent. And as noted, the parties do not dispute that the Boston IV

lens achieved significant commercial success over prior Bausch & Lomb rigid contact lens

products. See FF. 169-171. Dome therefore is entitled to a presumption that this commercial

success relates to claim 1 of the Boston IV lens. Demaco Corp. v. F. Von Langsdorff Licensing

55
Ltd., 851 F.2d at 1392. But several factors undercut the persuasiveness of the evidence offered

at trial.

First, the evidence of commercial success in the market is not particularly strong.

Although Dome introduced evidence that the Boston IV lens achieved significant commercial

success over prior Bausch & Lomb products, there is little evidence in the record of this

product’s success as compared to competitors’ products. Rather, other RGP lenses with

comparable or improved oxygen permeability levels came on the market at or near the same

time, and there is no evidence that the Neefe process was used in developing these lenses. See

JTX-4 at 206; JTX-26 at 11.3-11.4; JTX-27 at 23. Dome puts forth a narrative that could be

compelling – artisans struggling in vain to create an extended wear lens, a problem finally solved

by Neefe, to great commercial advantage – but provides no market data to support this narrative.

Second, on the issue of nexus, Dome has done little more than show that the

Boston IV lens falls within the scope of claim 1 and achieved some commercial success. To

bolster its nexus argument, Dome introduced the testimony of Dr. Mark Melamed, who

explained why oxygen permeability would be a desirable property, and the Court has no doubt

that increased oxygen permeability was one of the reasons for the Boston IV’s popularity. See

FF. 8-13, 81, 168. But Dr. Melamed’s suggestion that oxygen permeability drove Boston IV’s

success is not reliable expert testimony, as such statements are outside the scope of his medical

expertise. Moreover, Dr. Melamed himself indicated that at least some of the commercial

success of the Boston IV lens is due to factors other than the lens’ oxygen permeability – factors

such as the lenses’ durability, the ease of replacing them, and low long-term costs, as well as

heavy marketing by Bausch & Lomb. See FF. 172.

56
 Dome also attempted to show a nexus by contrasting the successful Boston IV

lens, which falls within claim 1, with the less successful Boston II lens, which, according to

Dome, does not. For the reasons described below – reasons that intersect with the

commensurateness requirement – this evidence is not persuasive.

iii. Commensurateness with the Scope of Claim 1

For evidence of secondary considerations such as commercial success to be

persuasive, the evidence “must be commensurate in scope with the claims which the evidence is

offered to support.” MeadWestVaco Corp. v. Rexam Beauty & Closures, Inc., 731 F.3d at

1264-65 (internal quotation omitted). Evidence of secondary considerations “is not

commensurate with the claims if the claims are broader than the scope” of such evidence. Joy

Technologies, Inc. v. Manbeck, 751 F. Supp. 225, 229 (D.D.C. 1990) aff’d, 959 F.2d 226 (Fed.

Cir. 1992). “The claims are broader in scope than the objective evidence if a limitation or

element recited in the claim is broader than the limitation or element in the objective evidence

. . . or if the objective evidence contains limitations or elements not recited in the claims.” Id. at

229-30 (citations omitted).

At least two rationales underlie the commensurateness requirement. First, a claim

can be patented only if it is nonobvious throughout the range of the patent claim. Evidence of

nonobviousness of one embodiment in a broad claim is of limited value, as it leaves open the

question of whether other embodiments were obvious. See, e.g., Therasense, Inc. v. Becton,

Dickinson & Co., 593 F.3d 1325, 1336 (Fed. Cir. 2010) (rejecting evidence that claimed

invention solved a longstanding problem, where claims were broad enough to cover both devices

that solved the problem and devices that did not); In re Clemens, 622 F.2d 1029, 1036 (C.C.P.A.

1980) (finding narrow range of data could not “be reasonably extended to prove the

57
unobviousness of a broader claimed range”); In re Tiffin, 448 F.2d 791, 792 (C.C.P.A. 1971)

(“the objective evidence of non-obviousness is not commensurate with the scope of claims 1-3

and 10-16, reciting ‘containers’ generally, but establishes non-obviousness only with respect to

‘cups’ and processes of making them”). Second, evidence that commercially desirable properties

are not commensurate with the patent claim suggests that the commercial success of one

particular embodiment results from something different (or more specific) than the claim. In

other words, if one embodiment of Neefe claim 1 has desirable properties, but another one does

not, claim 1 does not necessarily cause those desirable properties. Viewed this way, the

commensurateness requirement bears on the nexus inquiry, and has occasionally been described

as such. See Regent Lighting Corp. v. FL Indus., Inc., 60 F.3d 840, 1995 WL 331122, at *5

(Fed. Cir. 1995) (unpublished table disposition); Joy Technologies, Inc. v. Manbeck, 751 F.

Supp. at 229.

As a general matter, the requirement that evidence of secondary considerations be

reasonably commensurate with the scope of the claim “does not mean that an applicant is

required to test every embodiment within the scope of his or her claims.” In re Kao, 639 F.3d

1057, 1068 (Fed. Cir. 2011); In re DBC, 545 F.3d at 1384 (“[A] patentee need not show that all

possible embodiments within the claims were successfully commercialized in order to rely on the

success in the marketplace of the embodiment that was commercialized.”) (internal quotation

omitted). The Federal Circuit has recognized that it is “unlikely that a company would sell a

product containing multiple, redundant embodiments of a patented invention.” In re Glatt Air

Techniques, Inc., 630 F.3d 1026, 1030 (Fed. Cir. 2011). Thus, “[i]f an applicant demonstrates

that an embodiment has an unexpected result and provides an adequate basis to support the

conclusion that other embodiments falling within the claim will behave in the same manner, this

58
will generally establish that the evidence [of secondary considerations such as unexpected results

and commercial success] is commensurate with scope of the claims.” In re Kao, 639 F.3d at

1068 (emphasis added). Where it appears that commercially desirable properties appear only in

a subset of a patent’s embodiments, however, a court may not extend evidence of commercial

success to the entire patent range. See In re Peterson, 315 F.3d at 1331 (affirming finding of

obviousness where patent applicant claimed alloy with 1% to 3% rhenium and presented

unexpected results only for alloy with 2% rhenium, where evidence suggested that alloy with 3%

rhenium possessed inferior properties). Dome’s evidence of commercial success falls into the

latter category, as there are several reasons to doubt that other embodiments of claim 1 will

behave in the same manner – i.e., achieve the same commercially desirable levels of oxygen

permeability – as the Boston IV lens.

First, it is undisputed that the material first manufactured by Neefe in accordance

with his patent had a Dk value of 14. This level is only marginally better than the oxygen

permeability levels obtained by the Polycon II lens based on Gaylord’s patent, and is in the range

obtained by the Boston II lens based on Ellis’s patent. See FF. 40 (noting the 10 to 12 Dk for

Polycon II lenses); FF. 148 (12-14 Dk for Boston II lenses). Dome agrees that this oxygen

permeability level would be insufficient for prolonged daily wear and would not drive

commercial success. See Dome Prop. Concl. Law 400 (discussing how the Boston II lens, with a

Dk value of 12 to 14, accounted for only 10% of Bausch & Lomb’s total material sales

distribution).

Second, as noted supra at FF. 177, the evidence indicates that a contact lens

material comprised of 35.5% to 41.7% by weight Tris monomer, 21.8% by weight ester of

acrylic or methacrylic acid, 9.9% by weight surface wetting agents tetraethyleneglycol

59
dimethacrylate and N-Nvinylpyrrolidone, and between .01% and 6.2% by weight Tris dimer and

trimer – all amounts falling within the range specified in claim 1 of the Neefe Patent – and

manufactured in accordance with that claim would have an oxygen permeability around 12 to 14

Dk. See FF. 131, 134, 137, 140, 142, 144, 148. This expectation would be reasonable because

the Boston II lens, which has this composition, see FF. 131, 134, 137, 140, 142, has an oxygen

permeability of 12 to 14 Dk, see FF. 148. Dome notes that the Boston II lens differs from the

claim 1 process in that a Tris-based cross-linker is not deliberately added to the Boston II

material – rather, it is a byproduct created during the process of making the Tris monomer, and it

simply remains in the mixture. But the evidence indicates that this distinction is not a

meaningful one in terms of the end result. As Dr. Long explained, Tris dimer and trimer will

serve as cross-linking agents regardless of when they are created or added. FF. 144.20

Third, Dome provides minimal evidence that other successful products could be

manufactured with Neefe’s ingredients at other amounts within the ranges disclosed by Neefe,

despite the fact that the disclosed ranges are very broad. See FF. 76 (calling for (1) “from 5% to

90% by weight” of Tris, (2) from “3% to 90% by weight of an ester of acrylic or methacrylic

acid;” (3) “from 0.5% to 90% by weight of a surface wetting agent;” and (4) “from 0.01% to

90% by weight of an oxygen permeable crosslinking agent selected from the class of

multifunctional siloxanyl alkyl esters”). Other than the Boston IV lens, Dome presented

evidence of only one other highly oxygen permeable lens manufactured under claim 1 – the

20
The Director argues that the Boston II lens therefore falls within the scope of
claim 1 of the patent, arguing that step (f) should be construed as being satisfied so long as Tris
dimer and trimer were present in the TX-91 formula. Although the Court finds that the inclusion
of some amount of Tris dimer and trimer through the TX-91 formula, rather than the purposeful
addition of the same amount later, is unlikely to affect the end result, the Court is hesitant to
provide a definitive construction of step (f) or its equivalence without further expert evidence or
briefing. And it is unnecessary to do so to resolve the issue of obviousness in this case.
60
TransAire lens invented in 1984, with a Dk value of 45 – and did not introduce evidence on how

that lens was manufactured. See FF. 79. Dome’s expert, Dr. Long, could not provide an opinion

on whether polymers containing comonomers in amounts at the outer ends of the ranges

identified by Neefe would have high oxygen permeability. FF. 173.

Although the Boston IV lens had increased oxygen permeability and achieved

commercial success, there is not “an adequate basis to support the conclusion that other

embodiments falling within [claim 1 of the Neefe Patent] will behave in the same manner.” In re

Kao, 639 F.3d at 1068. That is, there is no basis for inferring that other embodiments throughout

the range of claim 1 will demonstrate high levels of oxygen permeability or achieve commercial

success. Dome has thus failed to present evidence of commercial success that is commensurate

with the broad scope of claim 1 of the Neefe Patent.

b. Satisfaction of Long-Felt Need and Failure of Others

Although Dome focuses mainly on evidence of commercial success, Dome also

argues that the Court should consider evidence of a long-felt, unsatisfied need for a contact lens

suitable for prolonged daily wear, which Dome asserts was ultimately obtained through the claim

1 process, in the form of the Boston IV lens. Dome’s PFF. 279-302; Dome’s Prop. Concl. Law

52. Specifically, Dome points to the inventions of Novicky and Ellis as evidence that other

scientists struggled to create an oxygen permeable contact lens that could be worn comfortably

throughout the day. Novicky’s polymer had an oxygen permeability of 5 to 8 Dk, Ellis’s

61
polymer had an oxygen permeability of 12 to 14 Dk, and both were unsuitable for prolonged

daily wear.21

Dome’s arguments are undermined by the same commensurateness defect that

limits its evidence of commercial success. Although the record indicates that the Boston IV lens

satisfied the need for a lens suitable for a prolonged wearing day, the record is also clear that

other embodiments of claim 1 would fail to satisfy the long-felt need identified by Dome.22

c. Dome’s Evidence of Secondary Considerations Is Not Sufficient To Overcome the Prima
Facie Case of Obviousness.

Even where evidence of commercial success and other secondary considerations

is clear and commensurate with a patent claim, it may be insufficient to outweigh a strong prima

facie case of obviousness. See Tokai Corp. v. Easton Enterprises, Inc., 632 F.3d at 1370 (“Even

if [the patentee] could establish the required nexus, a highly successful product alone would not

overcome the strong showing of obviousness.”) (internal quotation omitted); Wyers v. Master

Lock Co., 616 F.3d at 1246 (collecting cases). Given that the evidence of secondary

considerations in this case is neither compelling nor commensurate with the patent claim, the

Court concludes that Dome has not rebutted the Director’s strong prima facie showing of

obviousness.

21
Dome also presented limited evidence relating to the process developed by
Donald J. Ratkowski and Ping-Chang Lue, which led to a patent issued on December 6, 1983.
See JTX-10; Jan. 28 AM Tr. at 77:19–79:22 (Long).
22
The Court also notes that while the need for a highly oxygen permeable contact
lens was indisputably long-felt, only a relatively short amount of time passed between the
relevant teachings in the prior art and the introduction of the process recited in claim 1: Neefe
applied for his patent less than two years after Tanaka submitted his application.
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 IV. CONCLUSION

For the foregoing reasons, the Court finds that the differences between the process

recited in claim 1 of the Neefe Patent and the prior art “are such that the claimed invention as a

whole would have been obvious” before September 8, 1980 (the filing date of the Neefe Patent

application) “to a person having ordinary skill in the art” of the polymer chemistry of contact

lens material. 35 U.S.C. § 103. Accordingly, the decision of the Board of Patent Appeals and

Interferences will be upheld. An appropriate Order will issue this same day.

/s/
PAUL L. FRIEDMAN
United States District Judge
DATE: July 1, 2014

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 APPENDIX – TRIAL EXHIBITS

A. Joint Trial Exhibits 1-34

1. U.S. Patent No. 4,306,042 to Neefe, issued December 15, 1981.
2. Curriculum Vitae of Timothy E. Long, Ph.D.
3. POLYMER CHEMISTRY: AN INTRODUCTION (Malcolm P. Stevens, ed., 3d ed. 1999)
(Excerpts - title pages and pp. 3-1 0).
4. CONTACT LENSES (Anthony J. Phillips and Lynne Speedwell, eds., 5th ed. 2007)
(Excerpts - title pages and pp. 17-18, 60-64, 66-67, 206).
5. FITTING GUIDE FOR RIGID AND SOFT CONTACT LENSES: A PRACTICAL APPROACH
(Harold L. Stein, et al., eds., 4th ed. 2002) (Excerpts - title pages and pp. 167-68, 272).
6. U.S. Patent No. 3,377,371 to Quaal, issued April 9, 1968.
7. U.S. Patent No. 3,808,178 to Gaylord, issued April 30, 1974.
8. U.S. Patent No. 4,120,570 to Gaylord, issued October 17, 1978.
9. U.S. Patent No. 4,152,508 to Ellis et al., issued May 1, 1979.
10. U.S. Patent No. 4,419,505 to Ratkowski et al., issued December 6, 1983.
11. U.S. Patent No. 4,216,303 to Novicky et al., issued August 5, 1980.
12. FITTING GUIDE FOR RIGID AND SOFT CONTACT LENSES: A PRACTICAL APPROACH
(Harold L. Stein, et al., eds., 2d ed. 1984) (Excerpts - title pages and p. 238).
13. U.S. Patent No. 4,235,985 to Tanaka et al., issued November 25, 1980.
14. U.S. Patent No. 4,153,641 to Deichert, issued May 8, 1979.
15. U.S. Patent No. 4,189,546 to Deichert, issued February 19, 1980.
16. Decision of the Board of Patent Appeals and Interferences in Ex parte Neefe, dated July
31, 2007.
17. “Boston Product Information.” (Excerpt - BL24, BL31 ).
18. “Manufacturing of TX-91 Monomer.” (BL 1-23).
19. “Synthesis of Methacrylate/Siloxane Monomer,” dated November 17, 1978. (BL67-73).
20. Polymer Technology Corporation, PMA 820065 - Boston Lens II, Volumes 7, 9 and 11.
(Excerpts - BL8325-29, BL8344-48, and BL8478-8512).
21. Polymer Technology Corporation, Special Supplement to PMA 820065 - Boston Lens
II. (Excerpts - BL8553-57, BL8576-82, and BL8599-8603).
22. Polymer Technology Corporation, Premarket Approval Application for the Boston
Equalens. (Excerpts - BL8732-BL8742).
23. “Introducing the Boston Lens IV.” (BL4303).
24. Curriculum Vitae of Mark A Melamed, M.D.
25. 3 CUNNINGHAM’S MANUAL OF PRACTICAL ANATOMY (14th ed. 1979). (Excerpt - title
pages and p. 152).
26. CONTACT LENS FITTING, A CLINICAL TEXT ATLAS. (Frank J. Weinstock, ed., 1989).
(Excerpt - title pages and pp. 11.1-11.16).

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27. FITTING GUIDE FOR RIGID AND SOFT CONTACT LENSES: A PRACTICAL APPROACH
(Harold L. Stein, et al., eds., 4th ed. 2002) (Excerpt - title pages and pp. 167-68, 271-
79).
28. CONTACT LENSES: A GUIDE TO SELECTION, FITTING AND MANAGEMENT OF
COMPLICATIONS (Susan Stenson, ed., 1987). (Excerpt - title pages and p. 48).
29. CONTACT LENSES: A TEXTBOOK FOR PRACTITIONER AND STUDENT (Anthony J. Phillips
and Janet Stone, 3d ed., 1989). (Excerpt - title pages and p. 761).
30. Letter dated October 17, 1984 from Harold A. Stein, M.D. to Patrick J. Caroline of
Polymer Technology Corp.
31. Annual Report for the period of November 1987 to June 1988, Volume II. (Excerpt -
BL8282, BL8309).
32. Curriculum Vitae of William J. Benjamin, O.D., Ph.D.
33. Prosecution history of U.S. Patent No. 4,306,042 including references of record therein
34. Reexamination history of U.S. Patent 4,306,042 (Control No. 90/005,090)

B. Plaintiff’s Trial Exhibits 1-6

1. U. S. Patent No. 2,793,223, issued May 21, 1957.
2. Excerpt of Boston Product Guide (BL4760, BL4776) (1999)
3. Excerpt of Polymer Technology Consultants Reference Manual, Boston Lenses
Physical Properties (BL5507, BL5513) (1992)
4. Demonstrative Exhibit - Notebook tabs 1, 2,3, 9, 10, 11, 12, 13, 16, 18, 19
5. Demonstrative Exhibit - Flip Chart by Dr. Long
6. Demonstrative Exhibit Board

C. Defendant’s Trial Exhibits 1-2

1. William J. Benjamin & Quido A. Cappelli, Oxygen Permeability (Dk) of Thirty-Seven
Rigid Contact Lens Materials, 79 OPTOMETRY AND VISION SCIENCE 103 (2002).
2. Excerpts from Dr. Long’s deposition testimony (pp. 1-2, 94-122).

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