Prosecution Insights
Last updated: April 18, 2026
Application No. 17/571,894

TETRAVALENT BISPECIFIC ANTIBODY AGAINST PD-1 AND VEGF, PREPARATION METHOD THEREFOR, AND USE THEREOF

Non-Final OA §112§DP
Filed
Jan 10, 2022
Examiner
HOPKINS, SAMANTHA LAKE
Art Unit
1641
Tech Center
1600 — Biotechnology & Organic Chemistry
Assignee
Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd.
OA Round
3 (Non-Final)
62%
Grant Probability
Moderate
3-4
OA Rounds
4y 0m
To Grant
99%
With Interview

Examiner Intelligence

Grants 62% of resolved cases
62%
Career Allow Rate
21 granted / 34 resolved
+1.8% vs TC avg
Strong +56% interview lift
Without
With
+56.5%
Interview Lift
resolved cases with interview
Typical timeline
4y 0m
Avg Prosecution
30 currently pending
Career history
64
Total Applications
across all art units

Statute-Specific Performance

§101
1.2%
-38.8% vs TC avg
§103
24.9%
-15.1% vs TC avg
§102
16.5%
-23.5% vs TC avg
§112
36.1%
-3.9% vs TC avg
Black line = Tech Center average estimate • Based on career data from 34 resolved cases

Office Action

§112 §DP
DETAILED ACTION 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 . Continued Examination Under 37 CFR 1.114 A request for continued examination under 37 CFR 1.114, including the fee set forth in 37 CFR 1.17(e), was filed in this application after final rejection. Since this application is eligible for continued examination under 37 CFR 1.114, and the fee set forth in 37 CFR 1.17(e) has been timely paid, the finality of the previous Office action has been withdrawn pursuant to 37 CFR 1.114. Applicant's submission filed on 16MAR2026 has been entered. Election/Restrictions Upon further evaluation, Applicant’s request to rejoin the withdrawn claims is noted but the request is not granted because the elected product is not allowable due to a new rejection as a result of the amended claims filed in the response filed on 16MAR2026. Claim Status Applicant’s amendments received 16MAR2026 are acknowledged. Claims 1, 3, 5, 7, 9, and 16 have been amended. Claims 17-48 are new. Claims 1-48 are pending in the instant application (i.e., Claim(s) 1, 17, and 33 is/are independent). Claims 2-9, 11-16, 18-25, 27-32, 34-41, and 43-48 remain withdrawn. Claims 1, 10, 17, 26, 33, and 42 are examined on the merits. Priority The present application is a CON of US Patent Application No. 17/617516, filed 08DEC2021, which is a PCT International Application No. PCT/CN2021/088153, filed 19APR2021, which claims foreign priority under 35 U.S.C. 119 (a)-(d). The certified copy of CN202010357134.4 filed on 29APR2020 has been received and is acknowledged. Information Disclosure Statement The information disclosure statement(s) (IDS) submitted on 20JAN2026 is/are acknowledged and the references cited therein have been considered. Double Patenting Applicant’s arguments, see p 10, Response to double patenting rejection section, filed 16MAR2026, with respect to the rejection(s) of claim(s) 1 and 10 under (provisional) non-statutory double patenting have been fully considered and said provisional rejections of claim(s) 1 and 10 have been withdrawn in view of the express abandonment of the co-pending application 17/617516. Claim Objections Claim 1 is objected to because of the following informalities: Claim 1 has an inadvertent typographical error which has already been noted in the interview on 23MAR2026, a second “[“ bracket is missing in line 4 of the claim. Appropriate correction is required. Claim Rejections - 35 USC § 112 The following is a quotation of the first paragraph of 35 U.S.C. 112(a): (a) IN GENERAL.—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 or joint inventor of carrying out the invention. The following is a quotation of the first paragraph of pre-AIA 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 1 and 10 are rejected under 35 U.S.C. 112(a) or 35 U.S.C. 112 (pre-AIA ), first paragraph, because the specification, while being enabling and providing written description for: “A PD1 x VEGF tetravalent bispecific antibody, comprising two polypeptide chains and four common light chains, the amino acid sequence of each of the two polypeptide chains comprises SEQ ID NOs: 16, 18, or 21 and the amino acid sequence of each of the four common light chains comprises SEQ ID NO: 13;” does not reasonably provide enablement or support for more. Claim 10 is also rejected since it depends from claim 1 but does not remedy this deficiency. Upon further consideration following the interview on 12MAR2026, Examiner notes that the amendment to claim 1 lacks full enablement and written description support. Specifically, the specification provides support for effective pairing of a specific combination of Fab-Fab-IgG4 heavy chains (i.e., polypeptide chains), wherein each of the two polypeptide chains are the same and comprise the amino acid sequence of SEQ ID NOs: 16, 18, or 21 and wherein each of the four common light chains comprise the amino acid sequence of SEQ ID NO: 13. Allowable Subject Matter Examiner notes that PD1 x VEGF tetravalent bispecific antibodies comprising SEQ ID NOs: 16, 18, or 21, and SEQ ID NO: 13 are free of the prior art. It is also noted that as currently claimed, claims 17, 26, 33, and 42 are allowed as they are free of the prior art. Conclusion Claims 1 and 10 are rejected. Claims 17, 26, 33, and 42 are allowed. Any inquiry concerning this communication or earlier communications from the examiner should be directed to SAMANTHA L. HOPKINS whose telephone number is (703)756-4666. The examiner can normally be reached Mon-Thurs 6:00 AM to 4:00 PM 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, Misook Yu can be reached at (571)272-0839. 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. /SAMANTHA LAKE HOPKINS/Examiner, Art Unit 1641 /MISOOK YU/Supervisory Patent Examiner, Art Unit 1641
Read full office action

Prosecution Timeline

Jan 10, 2022
Application Filed
Apr 30, 2025
Non-Final Rejection — §112, §DP
Oct 06, 2025
Response Filed
Dec 05, 2025
Final Rejection — §112, §DP
Mar 16, 2026
Request for Continued Examination
Mar 18, 2026
Response after Non-Final Action
Mar 23, 2026
Applicant Interview (Telephonic)
Apr 04, 2026
Non-Final Rejection — §112, §DP (current)

Precedent Cases

Applications granted by this same examiner with similar technology

Patent 12599650
INHIBITIONS OF SIRP-GAMMA FOR CANCER TREATMENT
2y 5m to grant Granted Apr 14, 2026
Patent 12595303
ANTIBODIES AND CHIMERIC ANTIGEN RECEPTORS THAT TARGET TACI
2y 5m to grant Granted Apr 07, 2026
Patent 12590149
ANTIBODY AND BISPECIFIC ANTIBODY TARGETING LAG-3 AND USE THEREOF
2y 5m to grant Granted Mar 31, 2026
Patent 12570742
ANTI-SIRPalpha MONOCLONAL ANTIBODIES AND USES THEREOF
2y 5m to grant Granted Mar 10, 2026
Patent 12552863
HIGH AFFINITY ANTI-CD3 ANTIBODIES, AND METHODS FOR THEIR GENERATION AND USE
2y 5m to grant Granted Feb 17, 2026
Study what changed to get past this examiner. Based on 5 most recent grants.

AI Strategy Recommendation

Get an AI-powered prosecution strategy using examiner precedents, rejection analysis, and claim mapping.
Powered by AI — typically takes 5-10 seconds

Prosecution Projections

3-4
Expected OA Rounds
62%
Grant Probability
99%
With Interview (+56.5%)
4y 0m
Median Time to Grant
High
PTA Risk
Based on 34 resolved cases by this examiner. Grant probability derived from career allow 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