Prosecution Insights
Last updated: August 06, 2026
Application No. 18/377,702

PD-L1-SPECIFIC ANTIBODIES AND METHODS OF USING THE SAME

Non-Final OA §DP
Filed
Oct 06, 2023
Priority
Jun 29, 2016 — provisional 62/356,105 +2 more
Examiner
OUSPENSKI, ILIA I
Art Unit
Tech Center
Assignee
Checkpoint Therapeutics Inc.
OA Round
1 (Non-Final)
78%
Grant Probability
Favorable
1-2
OA Rounds
0m
Est. Remaining
98%
With Interview

Examiner Intelligence

Grants 78% — above average
78%
Career Allowance Rate
866 granted / 1117 resolved
+17.5% vs TC avg
Strong +20% interview lift
Without
With
+20.4%
Interview Lift
resolved cases with interview
Typical timeline
2y 8m
Avg Prosecution
40 currently pending
Career history
1160
Total Applications
across all art units

Statute-Specific Performance

§101
3.8%
-36.2% vs TC avg
§103
9.5%
-30.5% vs TC avg
§102
20.4%
-19.6% vs TC avg
§112
38.2%
-1.8% vs TC avg
Black line = Tech Center average estimate • Based on career data from 1117 resolved cases

Office Action

§DP
DETAILED ACTION 1. The present application, filed on or after March 16, 2013, is being examined under the first inventor to file provisions of the AIA . 2. Applicant's preliminary amendment filed on 01/25/2024 is acknowledged. Claims 25-44 are pending. 3. 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. A nonstatutory double patenting rejection is appropriate where the conflicting claims are not identical, but at least one examined application claim is not patentably distinct from the reference claim(s) because the examined application claim is either anticipated by, or would have been obvious over, the reference claim(s). See, e.g., In re Berg, 140 F.3d 1428, 46 USPQ2d 1226 (Fed. Cir. 1998); 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); In re Thorington, 418 F.2d 528, 163 USPQ 644 (CCPA 1969). A timely filed terminal disclaimer in compliance with 37 CFR 1.321(c) or 1.321(d) may be used to overcome an actual or provisional rejection based on nonstatutory double patenting provided the reference application or patent either is shown to be commonly owned with the examined application, or claims an invention made as a result of activities undertaken within the scope of a joint research agreement. See MPEP § 717.02 for applications subject to examination under the first inventor to file provisions of the AIA as explained in MPEP § 2159. See MPEP §§ 706.02(l)(1) - 706.02(l)(3) for applications not subject to examination under the first inventor to file provisions of the AIA . A terminal disclaimer must be signed in compliance with 37 CFR 1.321(b). The USPTO Internet website contains terminal disclaimer forms which may be used. Please visit www.uspto.gov/patent/patents-forms. The filing date of the application in which the form is filed determines what form (e.g., PTO/SB/25, PTO/SB/26, PTO/AIA /25, or PTO/AIA /26) should be used. A web-based eTerminal Disclaimer may be filled out completely online using web-screens. An eTerminal Disclaimer that meets all requirements is auto-processed and approved immediately upon submission. For more information about eTerminal Disclaimers, refer to www.uspto.gov/patents/process/file/efs/guidance/eTD-info-I.jsp. 4. Claims 25-44 are rejected on the ground of nonstatutory double patenting as being unpatentable over the claims of U.S. Patents No. 10590199 and 11834505. Although the claims at issue are not identical, they are not patentably distinct from each other because the instant claims are anticipated by the claims of each of the above patents. The present application was filed as a continuation of USSN 16818621 issued as US ‘505, which was filed as a continuation of USSN 15636610 issued as US ‘199. The claims of each of US ‘199 and US ‘505 recite anti-PD-L1 antibodies comprising the same amino acid sequences of the constituent CDRs, VH, VL, heavy chain, and light chain as the anti-PD-L1 antibodies recited in instant claims (claims 1-18, 22, and 25-31 of US ‘199, and claims 1, 5, 11-17, 25, 27, 29 and 30 of US ‘505), thereby anticipating instant claims 25-36. The reference patents further claim methods of treating cancer comprising administering the anti-PD-L1 antibodies (claims 18-31 of US ‘199, and claims 1-31 of US ‘505), thereby anticipating instant claims 37-42. Claims 43-44 are included in the rejection, because the recited nucleic acid sequences encoding the heavy and light chains of the anti-PD-L1 antibodies are inherent in recombinantly produced anti-PD-L1 antibodies recited in the claims of each of the reference patents. 5. Conclusion: no claim is allowed. 6. Any inquiry concerning this communication or earlier communications from the examiner should be directed to ILIA I OUSPENSKI whose telephone number is (571)272-2920. The examiner can normally be reached 9 AM - 5:30 PM. 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, Julie Wu can be reached at 571-272-5205. 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. /ILIA I OUSPENSKI/ Primary Examiner, Art Unit 1644
Read full office action

Prosecution Timeline

Oct 06, 2023
Application Filed
Jul 16, 2026
Non-Final Rejection mailed — §DP (current)

Precedent Cases

Applications granted by this same examiner with similar technology

Patent 12698512
METHODS COMPRISING ONCOLYTIC VIRUSES EXPRESSING CD19T AND BISPECIFIC T CELL ENGAGERS
1y 9m to grant Granted Aug 04, 2026
Patent 12692316
ANTIBODIES TO CANINE INTERLEUKIN-4 RECEPTOR ALPHA
4y 1m to grant Granted Jul 28, 2026
Patent 12686712
ANTIBODY, RELATED USE, PHARMACEUTICAL COMPOSITION INCLUDING METHOD FOR DIAGNOSING FUNGAL INFECTIONS, FUNGAL INFECTION DIAGNOSIS KIT AND METHOD FOR TREATING FUNGAL INFECTIONS
3y 11m to grant Granted Jul 21, 2026
Patent 12686718
TARGETED BINDING AGENTS AGAINST B7-H1
3y 8m to grant Granted Jul 21, 2026
Patent 12686716
CANCER IMMUNOTHERAPY BY DISRUPTING PD-1/PD-L1 SIGNALING
1y 2m to grant Granted Jul 21, 2026
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
98%
With Interview (+20.4%)
2y 8m (~0m remaining)
Median Time to Grant
Low
PTA Risk
Based on 1117 resolved cases by this examiner. Grant probability derived from career allowance rate.

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