Prosecution Insights
Last updated: May 29, 2026
Application No. 18/254,261

NOVEL PAR-2 INHIBITORS

Non-Final OA §102§103
Filed
May 24, 2023
Priority
Dec 03, 2020 — EU 20306495.1 +1 more
Examiner
PECKHAM, RICHARD GRANT
Art Unit
1627
Tech Center
1600 — Biotechnology & Organic Chemistry
Assignee
Domain Therapeutics
OA Round
1 (Non-Final)
68%
Grant Probability
Favorable
1-2
OA Rounds
2m
Est. Remaining
99%
With Interview

Examiner Intelligence

Grants 68% — above average
68%
Career Allowance Rate
82 granted / 120 resolved
+8.3% vs TC avg
Strong +36% interview lift
Without
With
+35.6%
Interview Lift
resolved cases with interview
Typical timeline
3y 2m
Avg Prosecution
43 currently pending
Career history
166
Total Applications
across all art units

Statute-Specific Performance

§101
2.6%
-37.4% vs TC avg
§103
32.9%
-7.1% vs TC avg
§102
4.6%
-35.4% vs TC avg
§112
15.3%
-24.7% vs TC avg
Black line = Tech Center average estimate • Based on career data from 120 resolved cases

Office Action

§102 §103
Notice of Pre-AIA or AIA Status The present application, filed on or after March 16, 2013, is being examined under the first inventor to file provisions of the AIA . Detailed Action Claims 1-2, 4, and 6-22 are currently pending. Election/Restriction Applicant’s election without traverse of Group I (Claims 1-2, 4, and 6-15, drawn to PAR-2 inhibitor compounds) and the elected species PNG media_image1.png 133 146 media_image1.png Greyscale in the reply filed on 2/06/2026 is acknowledged. Claims 14 and 16-22 are withdrawn from further consideration pursuant to 37 CFR 1.142(b) as being drawn to nonelected Group II or unelected species, there being no allowable generic or linking claim. Thus, Claims 1-2, 4, 6-13, and 15 are being examined on the merits herein. The requirement is deemed proper and is therefore made final. In the event the determination of the status of the application as subject to AIA 35 U.S.C. 102 and 103 (or as subject to pre-AIA 35 U.S.C. 102 and 103) is incorrect, any correction of the statutory basis (i.e., changing from AIA to pre-AIA ) for the rejection will not be considered a new ground of rejection if the prior art relied upon, and the rationale supporting the rejection, would be the same under either status. Claim Rejections - 35 USC § 102 The following is a quotation of the appropriate paragraphs of 35 U.S.C. 102 that form the basis for the rejections under this section made in this Office action: A person shall be entitled to a patent unless – (a)(1) the claimed invention was patented, described in a printed publication, or in public use, on sale, or otherwise available to the public before the effective filing date of the claimed invention. Claims 1-2, 4, 6-11, and 15 are rejected under 35 U.S.C. 102(a)(1) as being anticipated by Shen (WO2018093696). Shen teaches DGAT2 inhibitors including Compound 23 on Page 71: PNG media_image2.png 181 222 media_image2.png Greyscale , in which the following definitions of examined formula (I) apply: X1 and X2 are nitrogen; X3, X4, X5, X6, X7, and X8 are carbon; L is CO; A is an 8-membered heterocyclyl; RX1 is aryl substituted with a halogen; and RX3 is phenyl-RX31, wherein RX31 is halogen. The compound is formulated in compositions comprising carriers and additives (Page 43, Lines 24-28). Claims 1-2, 4, 6, 9-11, and 15 are rejected under 35 U.S.C. 102(a)(1) as being anticipated by Barr (WO2014028597). Barr teaches RORgammaT inhibitors including Compound 4M on Page 72: PNG media_image3.png 221 229 media_image3.png Greyscale , in which the following definitions of examined formula (I) apply: X1 and X2 are nitrogen; X3, X4, X5, X6, X7, and X8 are carbon; L is CO; A is a 6-membered heterocyclyl substituted with two RA, wherein both are methyl; RX1 is C1-alkylene-aryl substituted with a halogen and haloalkyl (RCYC[Wingdings font/0xE0]-L1-RL1, wherein L1 is a bond) and the CH2 of alkylene is replaced by -CO-; and RX3 is -LX3-carbocyclyl substituted with RX31, wherein LX3 is a bond and RX31 is –(C0alkylene)-COOH. Barr teaches the compound in a pharmaceutical composition with excipients (Page 32). Claim Rejections - 35 USC § 103 The following is a quotation of 35 U.S.C. 103 which forms the basis for all obviousness rejections set forth in this Office action: A patent for a claimed invention may not be obtained, notwithstanding that the claimed invention is not identically disclosed as set forth in section 102, if the differences between the claimed invention and the prior art are such that the claimed invention as a whole would have been obvious before the effective filing date of the claimed invention to a person having ordinary skill in the art to which the claimed invention pertains. Patentability shall not be negated by the manner in which the invention was made. Claims 1-2, 4, 6, 9-12, and 15 are rejected under 35 U.S.C. 103 as being unpatentable over Barr (WO2014028597). Barr teaches RORgammaT inhibitors including Compound 4M on Page 72: PNG media_image3.png 221 229 media_image3.png Greyscale , in which the following definitions of examined formula (I) apply: X1 and X2 are nitrogen; X3, X4, X5, X6, X7, and X8 are carbon; L is CO; A is a 6-membered heterocyclyl substituted with two RA, wherein both are methyl; RX1 is C1-alkylene-aryl substituted with a halogen and haloalkyl (RCYC[Wingdings font/0xE0]-L1-RL1, wherein L1 is a bond) and the CH2 of alkylene is replaced by -CO-; and RX3 is -LX3-carbocyclyl substituted with RX31, wherein LX3 is a bond and RX31 is –(C0alkylene)-COOH. Barr teaches the compound in a pharmaceutical composition with excipients (Page 32). Regarding Claim 12, Barr does not restrict the placement of the two RA-corresponding alkyl substituents. Further, compounds which are position isomers (compounds having the same radicals in physically different positions on the same nucleus) are generally of sufficiently close structural similarity that there is a presumed expectation that such compounds possess similar properties. In re Wilder, 563 F.2d 457, 195 USPQ 426 (CCPA 1977). See MPEP 2144.09. One of skill in the art seeking to form a RORgammaT inhibitor as taught by Barr would then find it obvious to reposition a single methyl substituent to bond to an adjacent carbon such that both methyl RA substituents are on the same carbon as required by Claim 12 and expect that a RORgammaT inhibitor would successfully form before the filing date of the instant invention. One would expect success in view of the MPEP teaching and degree of variability taught by Barr with respect to the substitution of the corresponding A-ring structure. Conclusion No claim is allowable. Claim 13 is objected to as being dependent upon a rejected base claim, but would be allowable if rewritten in independent form including all of the limitations of the base claim and any intervening claims. Inquiries Any inquiry concerning this communication or earlier communications from the examiner should be directed to Richard G. Peckham whose telephone number is (703)756-4621. The examiner can normally be reached 8:30am - 4:30pm EST. Examiner interviews are available via telephone, in-person, and video conferencing using a USPTO supplied web-based collaboration tool. To schedule an interview, applicant is encouraged to use the USPTO Automated Interview Request (AIR) at http://www.uspto.gov/interviewpractice. If attempts to reach the examiner by telephone are unsuccessful, the examiner’s supervisor, Kortney Klinkel can be reached on (571) 270-5239. The fax phone number for the organization where this application or proceeding is assigned is 571-273-8300. Information regarding the status of published or unpublished applications may be obtained from Patent Center. Unpublished application information in Patent Center is available to registered users. To file and manage patent submissions in Patent Center, visit: https://patentcenter.uspto.gov. Visit https://www.uspto.gov/patents/apply/patent-center for more information about Patent Center and https://www.uspto.gov/patents/docx for information about filing in DOCX format. For additional questions, contact the Electronic Business Center (EBC) at 866-217-9197 (toll-free). If you would like assistance from a USPTO Customer Service Representative, call 800-786-9199 (IN USA OR CANADA) or 571-272-1000. /RICHARD GRANT PECKHAM/Examiner, Art Unit 1627 /Kortney L. Klinkel/Supervisory Patent Examiner, Art Unit 1627
Read full office action

Prosecution Timeline

May 24, 2023
Application Filed
Mar 30, 2026
Non-Final Rejection mailed — §102, §103 (current)

Precedent Cases

Applications granted by this same examiner with similar technology

Patent 12636290
BET INHIBITORS FOR MODULATING DUX4 EXPRESSION IN FSHD
4y 11m to grant Granted May 26, 2026
Patent 12624023
SULFONYLUREA DERIVATIVES AND USES THEREOF
4y 5m to grant Granted May 12, 2026
Patent 12606558
CONDENSED PYRAZOLE DERIVATIVES AS INHIBITORS OF SARM1
3y 6m to grant Granted Apr 21, 2026
Patent 12595243
MODULATORS OF EXTRACELLULAR SIGNAL-REGULATED KINASE
1y 5m to grant Granted Apr 07, 2026
Patent 12583859
PRMT5 INHIBITORS AND USES THEREOF
4y 6m to grant Granted Mar 24, 2026
Study what changed to get past this examiner. Based on 5 most recent grants.

Strategy Recommendation AI-generated — please review before filing

Get a prosecution strategy drawn from examiner precedents, rejection analysis, and claim mapping.
Typically takes 5-10 seconds — AI-generated, attorney review required before filing

Prosecution Projections

1-2
Expected OA Rounds
68%
Grant Probability
99%
With Interview (+35.6%)
3y 2m (~2m remaining)
Median Time to Grant
Low
PTA Risk
Based on 120 resolved cases by this examiner. Grant probability derived from career allowance rate.

Sign in with your work email

Enter your email to receive a magic link. No password needed.

Personal email addresses (Gmail, Yahoo, etc.) are not accepted.

Free tier: 3 strategy analyses per month