Federal Circuit disposition — 23-1063

N OTE: This disposition is nonprecedential.
United States Court of Appeals
for the Federal Circuit
______________________
IN RE: ADVANCED CELL DIAGNOSTICS, INC.,
Appellant
______________________
2023-1063
______________________
Appeal from the United States Patent and Trademark
Office, Patent Trial and Appeal Board in No. 17/012,394.
______________________
Decided: July 18, 2024
______________________
ANNE M. REYNOLDS , Casimir Jones, SC, Middleton, WI,
argued for appellant. Also represented by J OHN MITCHELL
J ONES .
SARAH E. CRAVEN, Office of the Solicitor, United States
Patent and Trademark Office, Alexandria, VA, argued for
appellee Katherine K. Vidal. Also represented by K AKOLI
CAPRIHAN, AMY J. N ELSON, F ARHEENA YASMEEN RASHEED.
______________________
Before P ROST , SCHALL , and REYNA, Circuit Judges.
REYNA, Circuit Judge.
Advanced Cell Diagnostics, Inc. appeals a decision of
the United States Patent Trial and Appeal Board sustain-
ing the examiner’s final rejection of certain claims of U.S.
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IN RE: ADVANCED CELL DIAGNOSTICS, INC. 2
Patent Application No. 17/012,394. ACD does not dispute
that the prior art combination at issue discloses the limita-
tions of the claims on appeal. Rather, ACD challenges the
Board’s motivation to combine and reasonable expectation
of success findings, as well as the Board’s consideration of
two expert declarations. Because we determine that the
Board’s findings are supported by substantial evidence and
that the Board did not err in its consideration of ACD’s ex-
pert declarations, we affirm.
BACKGROUND
I. The ’394 Application
Applicant Advanced Cell Diagnostics, Inc. (“ACD”)
filed U.S. Patent Application No. 17/012,394 (“’394 applica-
tion”) with the United States Patent and Trademark Office
(“PTO”). The technology at issue relates to in situ hybridi-
zation, a known method of localizing and detecting specific
nucleic acids in situ, i.e., in an intact cell. The ’394 appli-
cation describes a method for the detection of two or more
nucleic acid targets using capture and label probes using
in situ hybridization. Each capture probe in the claimed
method has a “T section” and an “L section.” The T section
hybridizes with a section of the target nucleic acid while
the L section hybridizes with a label probe.
As displayed below in Figure 4 of the application, the
claimed system uses sets of capture probes, with each set
comprising two separate capture probes, e.g., set 1 includ-
ing probe L1-T1 and probe L2-T2. Each set of capture
probes hybridizes to the target nucleic acid and to a label
probe (“LP”) that contains a detectable label, which is dis-
played as “SGP” below.
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IN RE: ADVANCED CELL DIAGNOSTICS, INC. 3
’394 application, Fig. 4.
According to the application, one advantage of the
claimed system is to increase stability and specificity of
binding among all pieces of the system. Previously, linkage
between a label probe and the target nucleic acid tended to
be unstable and fall off when only one capture probe was
in place. The claimed system, which uses multiple capture
probes, results in “exceptional specificity because the sig-
nal-generating label probe can only be attached to the tar-
get gene of interest when two independent capture probes
both recognize the target and bind to the adjacent se-
quences or in very close proximity of the target gene.”
J.A. 337, ¶ 202.
For purposes of this appeal, independent claim 98 of
the ’394 application is representative and recites in rele-
vant part:
98. A method of detecting two or more nucleic acid
targets within an individual cell, the method com-
prising:
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IN RE: ADVANCED CELL DIAGNOSTICS, INC. 4
providing a sample comprising the cell, which cell
comprises or is suspected of comprising two or more
nucleic acid targets;
providing for each nucleic acid target a label probe
system comprising two or more identical label
probe complexes, each of which comprises a nucleic
acid component and one or more labels, wherein
the labels of the label probe systems are distinct for
each target nucleic acid;
providing for each nucleic acid target a capture
probe system comprising two or more sets of cap-
ture probes, wherein each set of capture probes
comprises two or more different capture probes,
wherein all capture probes in the capture probe
system comprise a T section and an L section,
wherein the T section is a nucleic acid sequence
complementary to a section on the nucleic acid tar-
get and the L section is a nucleic acid sequence
complementary to a section on the nucleic acid com-
ponent of the label probe complex, and wherein the
T sections of the two or more different capture
probes are complementary to non-overlapping re-
gions of the nucleic acid target, and the L sections
of the two or more different capture probes are com-
plementary to nonoverlapping regions of the nu-
cleic acid component of the label probe complex;
hybridizing, in the cell and in the presence of cellu-
lar non-target nucleic acids, the capture probe sys-
tem to the two or more nucleic acid targets, when
present in the cell, thereby providing hybridization
of two or more different capture probe sets to a sin-
gle copy of the nucleic acid target molecules in the
presence of cellular non-target nucleic acids;
capturing, in the cell and in the presence of cellular
non-target nucleic acids, the label probe system to
the capture probe system hybridized to the nucleic
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IN RE: ADVANCED CELL DIAGNOSTICS, INC. 5
acid target molecules, wherein the capturing oc-
curs by simultaneously hybridizing the two or more
different capture probes in each capture probe set
to a single molecule of the nucleic acid component
of the label probe complex that is complementary
to the L sections of the two or more different cap-
ture probes, thereby capturing the two or more la-
bel probe complexes to the nucleic acid target in the
presence of cellular non-target nucleic acids; and
detecting a signal from the two or more label probe
complexes captured on the nucleic acid targets,
wherein the presence of a signal indicates the pres-
ence of the nucleic acid targets in the sample, and
the absence of a signal indicates the absence of the
nucleic acid targets in the sample.
’394 application, claim 98.
II. Prior Art
There are three prior art references at issue in this ap-
peal: Kenny,1 Urdea,2 and Ward.3 Kenny discloses a
method of in situ detection of one target nucleic acid in a
cell using T-L capture probes and a labeling system. Un-
like the application at issue, Kenny does not teach using
capture probe sets or detecting multiple nucleic acid tar-
gets.
Concerning the label probe system, Kenny discloses a
preferred embodiment, which includes a branched network
of probes that hybridize to a plurality of detectable label
probes. Kenny alternatively notes that other label probe
systems may work. Kenny discloses that once a capture
probe is hybridized to the target nucleic acid, “any method
1 WO 01/94632 A2, published Dec. 13, 2001.
2 U.S. Patent No. 5,681,697.
3 U.S. Patent No. 6,007,994.
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IN RE: ADVANCED CELL DIAGNOSTICS, INC. 6
that can detect [capture] probe complexes on the substrate
may be used to determine the presence of the nucleic acid
analyte.” J.A. 751, 13:20–21 (emphasis added).
Urdea discloses an in vitro hybridization method. An
in vitro environment is one where the target nucleic acids
are separated from the cellular environment and interact
with probe molecules tethered to a solid support.
Urdea additionally discloses hybridization using T-L
capture probes that hybridize with a target nucleic acid
and a label probe. Like the ’394 application, Urdea teaches
using sets of capture probes. According to Urdea, using
sets of capture probes provides a detectable signal of only
the target nucleic acid of interest and thus reduces “back-
ground noise” derived from non-specific hybridization and
non-specific binding.
Finally, Ward discloses a hybridization method to de-
tect multiple target nucleic acids. This process is referred
to as “multiplexing.”
III. Proceedings before the PTO
The examiner rejected independent claim 98 as obvious
in view of Kenny, Urdea, and Ward. The examiner also
rejected various dependent claims, which are not directly
at issue in this appeal.4
In support of its application, ACD submitted the decla-
rations of Dr. Mickey S. Urdea, a named co-inventor of
Urdea, and Dr. Daryn Kenny, a named co-inventor of
Kenny. Both declarants opined that at the time the appli-
cation at issue was filed, a skilled artisan would not have
4 ACD does not separately challenge the rejections of
any dependent claims and thus for this appeal, the follow-
ing claims will rise or fall with independent claim 98:
claims 99–104, 107, 108, 111–18, 120, and 121. Appellant
Br. 3 n. 1.
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IN RE: ADVANCED CELL DIAGNOSTICS, INC. 7
had a reasonable expectation of success in combining
Kenny, Urdea, and Ward. The examiner dismissed Dr.
Urdea’s testimony as “merely . . . the opinion of a someone
[sic] compensated for the opinion” and contradicted by the
record. J.A. 588. Similarly, the examiner dismissed Dr.
Kenny’s testimony as providing “only the paid declarants
[sic] opinion, but no evidence.” J.A. 593.
The Patent Trial and Appeal Board (“Board”) affirmed
the examiner’s rejection of claim 98 as obvious over Kenny,
Urdea, and Ward. The Board determined that these refer-
ences teach all of the limitations of claim 98: (1) Kenny
teaches an in situ hybridization method using capture
probes to detect a target nucleic acid, (2) Urdea teaches us-
ing sets of capture probes, and (3) Ward teaches hybridiza-
tion to two or more target nucleic acids (multiplexing). The
Board also found a skilled artisan would be motivated to
improve (1) Kenny’s in situ hybridization method by using
Urdea’s capture probe sets and label probe system to in-
crease specificity in detection of target nucleic acids and
(2) the Kenny and Urdea combination with Ward’s multi-
plexing system to allow for detection of multiple target nu-
cleic acids. J.A. 12–13. The Board then found a reasonable
expectation of success in arriving at the claimed invention
because the three references were based on “decades old,
basic nucleic acid hybridization technology” well known to
skilled artisans at the time of ACD’s claimed invention.
J.A. 16 (emphasis removed).
In arriving at these findings, the Board rejected ACD’s
declarations from Drs. Urdea and Kenny as unpersuasive.
The Board determined that these declarations failed to pro-
vide evidentiary support for the underlying opinions and
contradicted the teachings of the references at issue.
J.A. 17–20.
ACD appeals. We have jurisdiction under 35 U.S.C.
§ 141(a) and 28 U.S.C. § 1295(a)(4)(A).
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IN RE: ADVANCED CELL DIAGNOSTICS, INC. 8
D ISCUSSION
We “review Board decisions in accordance with the Ad-
ministrative Procedure Act, 5 U.S.C. § 706(2).” HTC Corp.
v. Cellular Commc’ns Equip., LLC, 877 F.3d 1361, 1367
(Fed. Cir. 2017). Obviousness is a question of law with un-
derlying factual findings relating to the scope and content
of the prior art; differences between the prior art and the
claims at issue; the level of ordinary skill in the pertinent
art; the presence or absence of a motivation to combine or
modify prior art with a reasonable expectation of success;
and any objective indicia of non-obviousness. Acoustic
Tech., Inc. v. Itron Networked Sols., Inc., 949 F.3d 1366,
1373 (Fed. Cir. 2020). We review the Board’s legal conclu-
sions de novo and its factual findings for substantial evi-
dence. HTC Corp., 877 F.3d at 1367. Substantial evidence
is “such relevant evidence as a reasonable mind might ac-
cept as adequate to support a conclusion.” Consol. Edison
Co. v. NLRB, 305 U.S. 197, 229 (1938). We do not reweigh
evidence on appeal. Impax Labs. Inc. v. Lannett Holdings
Inc., 893 F.3d 1372, 1382 (Fed. Cir. 2018).
On appeal, ACD challenges the Board’s motivation to
combine and reasonable expectation of success findings
and the Board’s consideration of the Urdea and Kenny dec-
larations. We address each challenge in turn.
I. Motivation to Combine
ACD challenges the Board’s motivation to combine de-
terminations in three respects. For the following reasons,
we reject ACD’s challenges.
We first determine that the Board’s motivation to com-
bine findings are supported by substantial evidence,
namely the references’ teachings. Here, the Board first de-
termined that a skilled artisan would have been motivated
to improve Kenny’s in situ method with Urdea’s capture
probe sets and label probe system for two reasons. First,
the Board relied on the examiner’s finding that a skilled
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IN RE: ADVANCED CELL DIAGNOSTICS, INC. 9
artisan would be motivated to combine the two because
Urdea teaches the use of capture probe sets to decrease
background noise and increase specificity. J.A. 12. Second,
as the Board noted, a skilled artisan would be motivated to
include Urdea’s system in Kenny’s because Kenny teaches
that once the capture probes hybridize to the target nucleic
acid, “any labeling probe or probe system . . . may be used
to hybridize to the L portion of the T-L probe.” J.A. 13 (cit-
ing Kenny’s teachings at J.A. 751, 13:19–22, which provide
that “any method that can detect the analyte-target probe
complexes . . . may be used to determine the presence of the
nucleic acid analyte” (emphasis added)).
The Board next determined that a skilled artisan
would have been motivated to combine Kenny and Urdea’s
combined capture and label probe system with Ward be-
cause Ward’s multiplexing process “would allow the detec-
tion of multiple sequences simultaneously.” J.A. 13
(quoting the examiner’s answer); see also J.A. 11 (citing
Ward’s teachings at J.A. 834, 2:55–60).
As the above shows, the Board rooted its motivation to
combine findings in the teachings of the references them-
selves. We thus affirm the Board’s motivation to combine
findings as supported by substantial evidence.
Turning now to ACD’s arguments to the contrary, ACD
first argues that the Board misunderstood the teachings of
Kenny and Urdea and thus, the Board’s motivation to com-
bine analysis was flawed. Appellant Br. 26. According to
ACD, Kenny needed to be modified with an additional cap-
ture probe in order to arrive at the claimed capture probe
set before it could be combined with Urdea’s label probe
system. Id. at 26–28, 41. ACD argues that the Board did
not consider this modification when concluding that a
skilled artisan would have been motivated to combine the
two references. Id. at 28. Rather, according to ACD, the
Board’s combination of these two references resulted in a
system that only had one capture probe hybridized to the
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IN RE: ADVANCED CELL DIAGNOSTICS, INC. 10
target nucleic acid, which does not meet the claimed cap-
ture probe set limitation.
The record, however, belies ACD’s argument. The
Board relied on the examiner’s rejection when determining
that a skilled artisan would be motivated to combine
Kenny with Urdea. J.A. 12. As the rejection notes, and the
Board found, a skilled artisan would have modified
Kenny’s one capture probe system “by use of the two or
more capture probe extenders hybridized and labeling probe
taught by Urdea in the in situ hybridization . . . method of
Kenny.” J.A. 12 (emphasis added) (quoting J.A. 678).
Thus, the combination the Board relied on included two or
more capture probes.
ACD next argues that even if the Board understood
that Kenny must be modified to include a second capture
probe, a skilled artisan would not be motivated to modify
Kenny in that manner. Appellant Br. 28–32. According to
ACD, Kenny’s in situ environment has the potential to re-
sult in off-target binding given that “an abundance of na-
tive cellular structures and components are present in the
samples, including off-target nucleic acids.” Id. at 28–29.
As such, ACD argues, a skilled artisan would expect that
including an additional probe in Kenny would result in ad-
ditional opportunities for off-target binding, reducing the
chances of a successful detection of the target. Id. at 29.
Substantial evidence, however, supports the Board’s
finding that a skilled artisan would have combined Kenny
with Urdea despite the differences in their assay environ-
ments. J.A. 15–17. The Board determined that (1) even in
situ, Kenny discloses a method for capture probes reaching
their intended targets without non-specific binding to cel-
lular components and (2) ACD even recognized this point
in its filings before the Board. J.A. 16–17 (citing J.A. 644,
ACD’s brief at 9). The Board also determined that, again
based on Kenny’s teachings, a skilled artisan would have
understood how to make and use a probe that does not bind
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IN RE: ADVANCED CELL DIAGNOSTICS, INC. 11
non-specifically in an in situ method. J.A. 13 (citing Kenny,
J.A. 751, 13:19–22); see also J.A. 15 (also citing Kenny,
J.A. 751, 13:19–22). This is substantial evidence. ACD’s
arguments to the contrary are an invitation to reweigh ev-
idence on appeal, which we cannot do. Impax Labs., 893
F.3d at 1382.
Finally, ACD argues that the Board erred in finding a
motivation to combine Ward with Kenny and Urdea. Ap-
pellant Br. 33–37. According to ACD, Ward teaches a more
simplified probe system than those disclosed in Kenny or
Urdea. Id. at 34. For this reason, and without fully ex-
plaining why, ACD argues that a skilled artisan would not
be motivated to combine Ward’s multiplexing system with
the Kenny and Urdea combination. Id. at 35–37.
The Board’s determination that a skilled artisan would
be motivated to combine Ward with Kenny and Urdea is
supported by substantial evidence. As previously dis-
cussed, the Board looked to Ward’s teachings of its multi-
plexing system and concluded that based on this evidence,
a skilled artisan would be motivated to include Ward’s mul-
tiplexing system because it “would allow the detection of
multiple sequences simultaneously.” J.A. 13; see also
J.A. 10. ACD’s conclusory argument that Ward’s simpli-
fied probe system somehow negates a motivation for
achieving simultaneous detection of nucleic acid targets is
a veiled invitation to reweigh evidence on appeal and thus
fails. Impax Labs., 893 F.3d at 1382.
II. Reasonable Expectation of Success
The Board determined that a skilled artisan would
have had a reasonable expectation of success in combining
the three references at issue. J.A. 12, 15–16. ACD argues
that this finding was “entirely conclusory” and thus im-
proper. Appellant Br. 32, 37–38. We disagree with ACD’s
argument.
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IN RE: ADVANCED CELL DIAGNOSTICS, INC. 12
“Evidence of a reasonable expectation of success, just
like evidence of a motivation to combine, may flow from the
prior art references themselves, the knowledge of one of or-
dinary skill in the art, or, in some cases, from the nature of
the problem to be solved.” Elekta Ltd. v. ZAP Surgical Sys.,
Inc., 81 F.4th 1368, 1377 (Fed. Cir. 2023) (citations and in-
ternal quotation marks omitted). Here, the Board first
found a skilled artisan would have reasonably expected
Urdea’s label probe system and capture probe sets to reach
their intended targets even in Kenny’s in situ environment.
See J.A. 15 (citing Kenny’s teachings at J.A. 751, 13:19–22).
Second, the Board found, based on Kenny’s teachings, that
a skilled artisan would have understood how to make and
use a probe that does not bind non-specifically in an in situ
method. J.A. 15 (citing Kenny’s teachings at J.A. 751,
13:19–20). Finally, the Board found that a skilled artisan
would have reasonably expected success in combining
Kenny and Urdea with Ward because such combination
was based on “decades old, basic nucleic acid hybridization
technology” that was well known in the art. J.A. 16 (em-
phasis in the original). The teachings of the three prior art
references, the nature of the technology at issue, and the
knowledge of one of ordinary skill in the art are sufficient
evidence to support the Board’s reasonable expectation of
success findings.
Moreover, we determine that the evidence supporting
the Board’s motivation to combine findings also support its
reasonable expectation of success findings. Here, ACD’s
reasonable expectation of success arguments are largely
duplicative of its motivation to combine arguments. Com-
pare Appellant Br. 26–32, 33–37 (motivation to combine ar-
guments) with id. 32–33, 37–38 (reasonable expectation of
success arguments); Oral Arg. 2:27–2:54, 10:50–11:03. In
some cases, when the arguments of reasonable expectation
of success are the same for motivation to combine, the evi-
dence establishing the latter may establish the former. El-
ekta, 81 F.4th at 1377. This is the case here.
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IN RE: ADVANCED CELL DIAGNOSTICS, INC. 13
We affirm the Board’s reasonable expectation of suc-
cess findings.
III. Expert Declarations
Finally, ACD argues that the Board’s decision is flawed
because it gave “insufficient consideration” to the Urdea
and Kenny declarations. Appellant Br. 38. The record,
however, shows otherwise. The Board sufficiently consid-
ered the two declarations and determined that they lacked
evidentiary support and ran counter to the teachings of the
three references at issue. J.A. 17–19. On these bases, the
Board determined the declarations were not persuasive.
Id. We see no error in this determination.
ACD argues that even if the Urdea and Kenny declara-
tions did not support the opinions expressed therein with
supporting evidence, the Board should have nonetheless
given the declarations “unique weight because they come
from named inventors of the references themselves.” Ap-
pellant Br. 45. ACD relies on In re Oelrich, 579 F.2d 86
(CCPA 1978), as support for this proposition.
We reject ACD’s argument for two reasons. First,
ACD’s position overlooks well-established precedent. “The
Board has broad discretion as to the weight to give to dec-
larations offered in the course of prosecution.” In re Am.
Acad. of Sci. Tech Ctr., 367 F.3d 1359, 1368 (Fed. Cir.
2004). “[T]he Board is entitled to weigh the declarations
and conclude that the lack of factual corroboration war-
rants discounting the opinions expressed in the declara-
tions.” Id. Indeed, a lack of factual support for expert
opinion going to factual determinations may render the tes-
timony of little probative value in a patentability determi-
nation. Ashland Oil, Inc. v. Delta Resins & Refractories,
Inc., 776 F.2d 281, 294 (Fed. Cir. 1985); see also Velander
v. Garner, 348 F.3d 1359, 1371 (Fed. Cir. 2003). That is
what happened here. The Board determined that the
Urdea and Kenny declarations lacked evidentiary support
for the underlying positions and for this reason, deemed
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IN RE: ADVANCED CELL DIAGNOSTICS, INC. 14
them unpersuasive. We see no abuse of discretion with this
determination.
Second, ACD’s position is unsupported by the law. To
hold that the Board must afford “unique weight” to unsup-
ported expert declarations solely because the expert was a
listed inventor of the prior art would result in a newfound
deference to expert declarations in prosecution proceed-
ings. We decline to create such a rule today.
Contrary to ACD’s position, In re Oelrich does not sup-
port the creation of this new level of deference. In In re
Oelrich, the United States Court of Customs and Patent
Appeals (“CCPA”), this court’s predecessor, determined
that the Board’s criticism of four affidavits was unwar-
ranted. 579 F.2d at 91. The CCPA recognized that the af-
fidavits reflected the opinions of skilled artisans with
unique competence. Id. However, the CCPA further ex-
plained that the affidavits were based on facts or on “tech-
nically sound applications of unquestioned physical
principles.” Id. Thus taken as a whole, the CCPA deter-
mined that the affidavits’ conclusions were reasonable and
credible. Id. Although ACD would argue otherwise, this
determination did not create a level of automatic deference
to skilled artisans based solely on their status as named
inventors. And in any event, unlike in In re Oelrich, the
Board here determined that the Urdea and Kenny declara-
tions were not supported by facts or unquestioned physical
principles. Thus, In re Oelrich is readily distinguishable
from this case.
In sum, we see no error in the Board’s consideration of
ACD’s expert declarations.
CONCLUSION
We have considered ACD’s other arguments and find
them unpersuasive. For the reasons stated above, we af-
firm the Board’s determination upholding the examiner’s
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IN RE: ADVANCED CELL DIAGNOSTICS, INC. 15
rejection of claims 98, 99–104, 107, 108, 111–18, 120, and
121 as obvious.
AFFIRMED
COSTS
No costs.
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