Case: 21-1115 Document: 58 Page: 1 Filed: 12/27/2021
NOTE: This disposition is nonprecedential.
United States Court of Appeals
for the Federal Circuit
______________________
QUEST DIAGNOSTICS INVESTMENTS LLC,
Appellant
v.
ANDREW HIRSHFELD, PERFORMING THE
FUNCTIONS AND DUTIES OF THE UNDER
SECRETARY OF COMMERCE FOR
INTELLECTUAL PROPERTY AND DIRECTOR OF
THE UNITED STATES PATENT AND TRADEMARK
OFFICE,
Intervenor
______________________
2021-1115
______________________
Appeal from the United States Patent and Trademark
Office, Patent Trial and Appeal Board in No. IPR2019-
00738.
______________________
Decided: December 27, 2021
______________________
THOMAS H. WINTNER, Mintz, Levin, Cohn, Ferris, Glov-
sky and Popeo, P.C., Boston, MA, for appellant. Also rep-
resented by PETER CUOMO; ADAM GAHTAN, Fenwick & West
LLP, New York, NY.
Case: 21-1115 Document: 58 Page: 2 Filed: 12/27/2021
2 QUEST DIAGNOSTICS INVESTMENTS LLC v. HIRSHFELD
ROBERT MCBRIDE, Office of the Solicitor, United States
Patent and Trademark Office, Alexandria, VA, for interve-
nor. Also represented by THOMAS W. KRAUSE, FARHEENA
YASMEEN RASHEED, MEREDITH HOPE SCHOENFELD.
______________________
Before MOORE, Chief Judge, CLEVENGER and CHEN,
Circuit Judges.
CHEN, Circuit Judge.
Quest Diagnostics Investments LLC (Quest) appeals a
decision of the Patent Trial and Appeal Board (Board) in
IPR2019-00738 finding claims 1, 2, and 4–14 of U.S. Patent
No. 8,409,862 (the ’862 patent) unpatentable as either an-
ticipated under 35 U.S.C. § 102 or obvious under 35 U.S.C.
§ 103. For the reasons stated herein, we affirm.
BACKGROUND
Quest owns the ’862 patent, which claims priority to
September 8, 2003 and is directed to using mass spectrom-
etry to detect low levels of testosterone in female humans.
See, e.g., ’862 patent col. 1 ll. 49–59, col. 5 ll. 50–65, claim
1. The ’862 patent explains that “[t]estosterone levels are
much lower in females compared to males” and “[t]he clin-
ical manifestations of excess testosterone in females in-
clude infertility, hirsutism, amenorrhea, and obesity.” Id.
col. 1 ll. 49–59. The ’862 patent further explains that tes-
tosterone can be purified prior to mass spectrometry, which
can improve the limit of detection (i.e., the lowest amount
of testosterone the method can detect). See, e.g., id. col. 3
ll. 7–21. Accordingly, the ’862 patent claims methods for
“determining the amount of testosterone in a sample”
where a user purifies the testosterone prior to mass spec-
trometry. Id. at claim 1. However, the ’862 patent explic-
itly excludes derivatization of testosterone before mass
Case: 21-1115 Document: 58 Page: 3 Filed: 12/27/2021
QUEST DIAGNOSTICS INVESTMENTS LLC v. HIRSHFELD 3
spectrometry, the lack of which Quest argues offers im-
provements in ease of use. 1 See id.
Claims 8 and 9, relevant here, depend upon claim 1 and
further require “wherein the method is capable of detecting
testosterone at concentrations of less than 5 ng/dL in the
sample” and “less than 1 ng/dL in the sample,” respec-
tively. Id. at claims 8–9.
On February 25, 2019, Laboratory Corporation of
America Holdings (LabCorp) petitioned for inter partes re-
view of claims 1, 2, and 4–14 of the ’862 patent. J.A. 79,
152. Relevant to this appeal, LabCorp asserted that claims
8 and 9 would have been obvious in view of Clarke, 2 or al-
ternatively would have been obvious in view of Clarke in
combination with Draisci. 3
Clarke is an abstract found on a compact disc (CD) from
the 49th annual conference of the American Society for
Mass Spectrometry (ASMS) held in May 2001. J.A. 1356–
57. Clarke details a method for detecting low levels of tes-
tosterone and describes a method similar to the ’862 pa-
tent—wherein testosterone is purified before mass
spectrometry. Lab’y Corp. of Am. Holdings v. Quest
1 Quest explains that derivatization of testosterone
is one method to improve detection of testosterone using
mass spectrometry. See Appellant’s Br. at 6–7. However,
Quest contends that the derivatization process can be labo-
rious and time consuming. See id.
2 Clarke, et al., Determination of Suppressed Testos-
terone Levels in Human Serum by LC-MS/MS, Proceed-
ings of the 49th ASMS Conference on Mass Spectrometry
and Allied Topics, Chicago, Illinois, May 27–31, 2001.
3 Draisci, et al., Quantitation of anabolic hormones
and their metabolites in bovine serum and urine by liquid
chromatography-tandem mass spectrometry, 870 J.
CHROMATOGRAPHY A, 511–22 (2000).
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4 QUEST DIAGNOSTICS INVESTMENTS LLC v. HIRSHFELD
Diagnostics Invs. LLC, 2020 WL 5224211, at *6–7 (P.T.A.B.
Sept. 1, 2020). Clarke claims to detect testosterone down
to 50 pg/mL—equivalent to 5 ng/dL.
C
On September 1, 2020, the Board issued its Final Writ-
ten Decision finding that claims 1, 2, and 4–14 would have
been unpatentable as either obvious or anticipated. See id.
at *1. Two of the Board’s findings are challenged here—
first, that Clarke was valid prior art as a printed publica-
tion and, second, that claims 8 and 9 would have been ob-
vious in light of Clarke or Clarke in combination with
Draisci.
As to whether Clarke is a printed publication, the
Board found Clarke was publicly available and therefore a
prior art printed publication. Specifically, the Board rec-
ognized that the ASMS sent a CD containing Clarke to
thousands of ASMS members, and that the CD was avail-
able in the University of Wisconsin-Madison library before
the priority date of the ’862 patent. See id. at *8–10. Fur-
ther, the Board noted that although Clarke appeared
alongside approximately 1,600 other abstracts, the CD per-
mitted users to search the abstracts using selected key-
words. See id. at *10. Given the dissemination,
accessibility, and searchability of the CD, the Board found
Clarke to be prior art. Id.
As to claims 8 and 9, the Board concluded it would have
been obvious to reach detection limits below 5 ng/dL and 1
ng/dL based on the teachings of Clarke or Clarke with
Draisci. The Board found that a skilled artisan would have
been motivated to achieve a lower level of detection and
have reached these levels by optimizing several experi-
mental parameters, specifically by “increasing the volume
of the sample” and “modernizing the equipment.” Id. at
*19–20.
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QUEST DIAGNOSTICS INVESTMENTS LLC v. HIRSHFELD 5
DISCUSSION
On appeal, Quest makes two arguments. 4 First, that
the Board erred in finding Clarke was publicly available
and thus the Board’s unpatentability determination as to
all challenged claims must be reversed. Second, that the
Board erred in holding that claims 8 and 9 would have been
obvious over Clarke and/or Clarke in view of Draisci. We
address each in turn.
A
Quest argues that Clarke was not a printed publication
because it was not publicly accessible. See Appellant’s Br.
at 40–55. “Whether a reference qualifies as a ‘printed pub-
lication’ . . . is a legal conclusion based on underlying fac-
tual findings.” Jazz Pharms., Inc. v. Amneal Pharms.,
LLC, 895 F.3d 1347, 1356 (Fed. Cir. 2018). We review the
Board’s legal determinations de novo and the underlying
factual findings for substantial evidence. Id. at 1355.
The Board found that the ASMS widely disseminated
the CD containing Clarke and that the CD was available in
a university library. See Lab’y, 2020 WL 5224211, at *7–
10. Quest largely ignores the ASMS’s public dissemination
and instead highlights that Clarke was a single abstract
out of approximately 1,600, all with minimal indexing. See
Appellant’s Br. at 43–45. Quest contends that this makes
Clarke an obscure, inaccessible reference. We disagree.
As this court has recognized, “the breadth of the dis-
semination [] to persons of ordinary skill is significant,”
and “[w]hether the disseminated material is addressed to
4 Initially, Quest also argued for reversal on the ba-
sis of unconstitutionality of inter partes review under the
Appointments Clause. See Appellant’s Br. at 56–57. How-
ever, Quest has since abandoned this argument. See ECF
No. 30.
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6 QUEST DIAGNOSTICS INVESTMENTS LLC v. HIRSHFELD
or of interest to persons of ordinary skill is also relevant to
the public accessibility inquiry.” Jazz Pharms., 895 F.3d
at 1357–58. Here, although Clarke was surrounded by
hundreds of other abstracts, the ASMS distributed the CD
to the specific people most motivated to search the CD and
find Clarke, a fact Quest does not dispute.
Moreover, the CD permitted keyword searching. While
the CD did not allow users to search the word “testos-
terone,” the CD permitted several mass spectrometry-re-
lated keywords. Lab’y, 2020 WL 5224211, at *10; see also
J.A. 1347–55 (listing search terms). Quest objects that
LabCorp did not identify the specific keywords the Board
ultimately relied on and presented no evidence that such
keywords could meaningfully narrow the abstracts. Appel-
lant’s Br. at 48–54. Nonetheless, given the wide dissemi-
nation of the CD, we are unpersuaded that any identified
limitations in searchability require finding Clarke inacces-
sible. As this court has already held, “a printed publication
need not be easily searchable after publication if it was suf-
ficiently disseminated at the time of its publication.” Suf-
folk Techs., LLC v. AOL Inc., 752 F.3d 1358, 1365 (Fed. Cir.
2014).
Accordingly, we conclude that substantial evidence
supports the Board’s finding that Clarke was publicly
available and thus prior art.
B
Quest also argues that the Board erred by holding that
claims 8 and 9 would have been obvious in light of Clarke
or Clarke in combination with Draisci. 5 “Whether a
claimed invention is unpatentable as obvious under § 103
is a question of law based on underlying findings of fact.”
5 Quest made no separate argument as to the patent-
ability of claims 1, 2, 4–7, and 10–14 other than Clarke not
being prior art.
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QUEST DIAGNOSTICS INVESTMENTS LLC v. HIRSHFELD 7
In re Gartside, 203 F.3d 1305, 1316 (Fed. Cir. 2000). We
review the legal conclusion of obviousness de novo and the
factual determinations for substantial evidence. See id.
As an initial matter, the parties dispute which precise
framework the Board applied in finding claims 8 and 9 ob-
vious—either the “routine optimization” analysis or the
“obvious-to-try” analysis. See Appellant’s Br. at 20–25. Re-
gardless of this distinction, the Board articulated a clear
motivation to modify and a clear reasonable expectation of
success, see Lab’y, 2020 WL 5224211, at *18–20, findings
that we conclude are supported by substantial evidence.
Specifically, Quest argues that there was no motivation
to modify Clarke to increase sensitivity, that there was no
reasonable expectation of success in doing so, and that
there was a documented failure of others. See Appellant’s
Br. at 26–40.
We find that substantial evidence supports the Board’s
conclusion that there was a motivation to improve the sen-
sitivity of methods measuring testosterone. The Board re-
lied on LabCorp’s expert testimony, as well as the scientific
papers underlying that expert testimony to conclude that
“measuring low testosterone levels are known to be clini-
cally relevant.” Lab’y, 2020 WL 5224211, at *18–19 (citing,
for example, J.A. 1228–29). Although Quest argues that 5
ng/dL and 1 ng/dL of testosterone are below the “‘clinically
relevant’ range of testosterone,” we are unpersuaded this
discourages developing more sensitive methods. Appel-
lant’s Br. at 26. In sum, we find that the Board had sub-
stantial evidence to find a motivation to modify Clarke to
reach 5 ng/dL and 1 ng/dL detection limits.
Turning to reasonable expectation of success, the
Board recognized a number of parameters a skilled artisan
could modify to reach 5 ng/dL or 1 ng/dL detection. Lab’y,
2020 WL 5224211, at *18–19. The Board focused on “in-
creasing sample volume” as a likely starting point. Id. at
*19. Neither party disputes that increasing sample volume
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8 QUEST DIAGNOSTICS INVESTMENTS LLC v. HIRSHFELD
would increase level of detection, and experts for both par-
ties agreed. Id. at *20, *24; see also J.A. 702 (LabCorp’s
expert stating that “one of skill in the art would have rou-
tinely identified the suitable volume to optimize sensitiv-
ity”), 2467 (Quest’s expert recognizing that increasing
sample volume “would increase the signal”). While Quest
contends that an increased sample volume would decrease
resolution, the claims at issue are silent as to resolution—
instead, the claims only refer to being “capable of detect-
ing.” ’862 patent at claims 1, 8, 9. Therefore, and particu-
larly when coupled with the Board’s consideration of other
parameters, we are persuaded that substantial evidence
supports the Board’s finding that a skilled artisan would
have had a reasonable expectation of success of achieving
a lower level of detection.
Lastly, we are unpersuaded by Quest’s argument that
the alleged failure of others establishes nonobviousness.
Quest points to a paper by Kushnir, et al. 6 Quest argues
that the paper demonstrates a failure of others to reach de-
tection levels of 5 ng/dL or 1 ng/dL without derivatizing
testosterone. Appellant’s Br. at 33–40. However, the
Board explicitly considered Kushnir and found that the
conditions were different and not indicative of failure to
achieve the relevant detection levels. Lab’y, 2020 WL
5224211, at *17, * 20. In particular, the Board noted dif-
ferences in equipment and “sample preparation methods.”
Id. Given the deferential standard of review, as well as the
differences in Kushnir’s detection method relative to the
claims at issue, we decline to say that the Board erred in
determining that Kushnir fails to establish nonobvious-
ness.
6 Kushnir, et al., Performance characteristics of a
novel tandem mass spectrometry assay for serum testos-
terone, 52(1) CLIN. CHEM. 120–28 (2006).
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QUEST DIAGNOSTICS INVESTMENTS LLC v. HIRSHFELD 9
In sum, we find that substantial evidence supports the
facts underlying the Board’s conclusion that claims 8 and 9
would have been obvious in light of Clarke. Because we
affirm the Board’s obviousness determination on Clarke
alone, we need not reach the combination of Clarke and
Draisci.
CONCLUSION
For the reasons set forth above, we affirm the Board’s
decision finding claims 1, 2, and 4–14 of the ’862 patent
unpatentable as either obvious or anticipated.
AFFIRMED