Prosecution Insights
Last updated: October 21, 2026
Application No. 18/915,226

HETEROCYCLIC COMPOUNDS AS BET INHIBITORS

Non-Final OA §112§DOUBLEPATENT
Filed
Oct 14, 2024
Priority
Jul 02, 2019 — provisional 62/870,020 +3 more
Examiner
RAHMANI, NILOOFAR
Art Unit
Tech Center
Assignee
Nuvation Bio Inc.
OA Round
1 (Non-Final)
78%
Grant Probability
Favorable
1-2
OA Rounds
0m
Est. Remaining
75%
With Interview

Examiner Intelligence

Grants 78% — above average
78%
Career Allowance Rate
889 granted / 1146 resolved
+17.6% vs TC avg
Minimal -3% lift
Without
With
+-2.9%
Interview Lift
resolved cases with interview
Fast prosecutor
1y 11m
Avg Prosecution
57 currently pending
Career history
1179
Total Applications
across all art units

Statute-Specific Performance

§101
2.8%
-37.2% vs TC avg
§103
14.1%
-25.9% vs TC avg
§102
27.5%
-12.5% vs TC avg
§112
39.0%
-1.0% vs TC avg
Black line = Tech Center average estimate • Based on career data from 1146 resolved cases

Office Action

§112 §DOUBLEPATENT
DETAILED ACTION Claims 24-26, 29-39 are pending in the instant application. 2. Claim Rejections - 35 USC § 112 The following is a quotation of the first paragraph of 35 U.S.C. 112: The specification shall contain a written description of the invention, and of the manner and process of making and using it, in such full, clear, concise, and exact terms as to enable any person skilled in the art to which it pertains, or with which it is most nearly connected, to make and use the same and shall set forth the best mode contemplated by the inventor of carrying out his invention. Claims 24-25, 29-39 are rejected under 35 U.S.C. 112, first paragraph, because the specification, while being enabling for inhibition of (BET), does not reasonably provide enablement for treating a disease mediated by (BET) or cancer. The specification does not enable any person skilled in the art to which it pertains, or with which it is most nearly connected, to make and/or use the invention commensurate in scope with these claims. There are many factors to be considered when determining whether there is sufficient evidence to support a determination that a disclosure does not satisfy the enablement requirement and whether any necessary experimentation is “undue”. These factors include 1) the breadth of the claims, 2) the nature of the invention, 3) the state of the prior art, 4) the level of one of ordinary skill, 5) the level of predictability in the art, 6) the amount of direction provided by the inventor, 7) the existence of working examples, and 8) the quantity of experimentation needed to make or use the invention based on the content of the disclosure. In re Wands, 858 F.2d 731, 737, 8 USPQ2d 1400, 1404 (Fed. Cir. 1988). 1) The breadth of the claims. 2) The nature of the invention, 3) The state of the prior art, 4) The level of one of ordinary skill, 5) The level of predictability in the art, 6) The amount of direction provided by the inventor, 7) The existence of working examples, 8) The quantity of experimentation needed to make or use the invention based on the content of the disclosure. The nature of the invention: The instant invention is drawn to method for treating a disease mediated by (BET), said method comprising administration of the compound or pharmaceutically acceptable salt thereof according to claim 24. The state of the prior art: As indicated by the prior art, there is not any association between (BET) inhibitors and treating a disease mediated by (BET). There is no guidance in the prior art that (BET) inhibitor could be useful to treat a disease mediated by (BET). The predictability in the art: At present using (BET) to treat a disease mediated by (BET) is purely speculative. It is noted that pharmaceutical art is unpredictable, requiring each embodiment to be individually assessed for physiological activity. In re Fisher, 427 F. 2d 833, 166 USPQ 18 (CCPA 1970) indicates that the more unpredictable an area is, the more specific enablement is necessary in order to satisfy the statute. They have not shown a nexus to treat diseases but have provided only reports in vitro which, absent a correlation to treat of diseases, are not sufficient to enable the invention. The level of the skill in the art: The level of skill in the art is high. Amount of guidance/working examples: Applicant provides examples of the test compounds to inhibit (BET) on pages 193-201. However, there is no guidance for using a therapeutically effective compound of Formula (I) to treat a disease mediated by (BET). The breadth of the claims: The claims encompass a method for treating a disease mediated by (BET). The quantity of experimentation needed: Since the guidance and teaching provided by the specification is insufficient for treating diseases associated with therapeutically effective amount of a compound of formula (I) is efficacious, one of ordinary skill in the art, even with high level of skill, is unable to use the instant compounds as claimed without undue experimentation. Taking all of the above into consideration, it is not seen where the instant claims 24-25, 29-39, for treating diseases associated with therapeutically effective amount of a compound of Formula (I) is efficacious, have been enabled by the instant specification. 3. Claim Rejections - Obvious Double Patenting The nonstatutory double patenting rejection is based on a judicially created doctrine grounded in public policy (a policy reflected in the statute) so as to prevent the unjustified or improper timewise extension of the “right to exclude” granted by a patent and to prevent possible harassment by multiple assignees. See In re Goodman, 11 F.3d 1046, 29 USPQ2d 2010 (Fed. Cir. 1993); In re Longi, 759 F.2d 887, 225 USPQ 645 (Fed. Cir. 1985); In re Van Ornum, 686 F.2d 937, 214 USPQ 761 (CCPA 1982); In re Vogel, 422 F.2d 438, 164 USPQ 619 (CCPA 1970); and, In re Thorington, 418 F.2d 528, 168 USPQ 644 (CCPA 1969). A timely filed terminal disclaimer in compliance with 37 CFR 1.321(c) may be used to overcome an actual or provisional rejection based on a nonstatutory double patenting ground provided the conflicting application or patent is shown to be commonly owned with this application. See 37 CFR 1.130 (b). Effective January 1,1994, a registered attorney or agent of record may sign a terminal disclaimer. A terminal disclaimer signed by the assignee must fully comply with 37 CFR 3.73(b). Claims 24-26, 29-39 are rejected under the judicially created doctrine obviousness-type double patenting as being unpatentable over the claims 1-31 of US 11,584,756. Although the conflicting claims are not identical, they are not patentably distinct from each other because the current invention embraces the invention claimed in the above patent. Determination of the scope and content of the prior art (MPEP §2141.01) ‘756 claims analogues chemical compound in claims 1-31 as the instant claims 24-26, 29-39. Ascertainment of the difference between the prior art and the claims (MPEP §2141.02) The difference between the instant claims 24-26, 29-39 and the claims 1-31 of ‘756 patent is that the claims are not word for word identical but the scope of the two sets of claims overlaps significantly with each other. Finding of prima facia obviousness-rational and motivation (MPEP §2142.2143) All the elements were known in prior art and one skilled in the art could have combined the elements as claimed by known methods with no change in their respective functions, and the combination would have yielded predictable results to one of ordinary skill in the art at the time of the invention. 4. Any inquiry concerning this communication or earlier communications from the examiner should be directed to Niloofar Rahmani whose telephone number is 571-272-4329. The examiner can normally be reached on Monday through Friday from 8:30 am to 5:00 pm. If attempts to reach the examiner by telephone are unsuccessful, the examiner’s supervisor, Renee Claytor, can be reached on 571-272-8394. The fax phone number for the organization where this application or proceeding is assigned is 703-872-9306. Information regarding the status of an application may be obtained from the Patent Application Information Retrieval (PAIR) system. Status information for published applications may be obtained from either Private PAIR or public PAIR. Status information for unpublished applications is available through Private PAIR only. For more information about the PAIR system, see http://pair-direct.uspto.gov. Should you have questions on access to the Private PAIR system, contact the Electronic Business Center (EBC) at 866-217-9197 (toll-free). /NILOOFAR RAHMANI/ Primary Examiner, Art Unit 1691 10/07/2026
Read full office action

Prosecution Timeline

Oct 14, 2024
Application Filed
Oct 09, 2026
Non-Final Rejection mailed — §112, §DOUBLEPATENT (current)

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Study what changed to get past this examiner. Based on 5 most recent grants.

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Prosecution Projections

1-2
Expected OA Rounds
78%
Grant Probability
75%
With Interview (-2.9%)
1y 11m (~0m remaining)
Median Time to Grant
Low
PTA Risk
Based on 1146 resolved cases by this examiner. Grant probability derived from career allowance rate.

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