Prosecution Insights
Last updated: April 19, 2026
Application No. 18/562,676

COMPOUNDS FOR DEGRADATION OF CYCLIN-DEPENDENT KINASE 7(CDK7)

Non-Final OA §112§DP
Filed
Nov 20, 2023
Examiner
RAHMANI, NILOOFAR
Art Unit
1691
Tech Center
1600 — Biotechnology & Organic Chemistry
Assignee
Qurient Co. Ltd.
OA Round
1 (Non-Final)
77%
Grant Probability
Favorable
1-2
OA Rounds
2y 1m
To Grant
74%
With Interview

Examiner Intelligence

Grants 77% — above average
77%
Career Allow Rate
871 granted / 1128 resolved
+17.2% vs TC avg
Minimal -3% lift
Without
With
+-2.9%
Interview Lift
resolved cases with interview
Fast prosecutor
2y 1m
Avg Prosecution
12 currently pending
Career history
1140
Total Applications
across all art units

Statute-Specific Performance

§101
2.2%
-37.8% vs TC avg
§103
12.6%
-27.4% vs TC avg
§102
25.2%
-14.8% vs TC avg
§112
35.8%
-4.2% vs TC avg
Black line = Tech Center average estimate • Based on career data from 1128 resolved cases

Office Action

§112 §DP
DETAILED ACTION Claims 1-27 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 21-27 are rejected under 35 U.S.C. 112, first paragraph, because the specification, while being enabling for inhibition of CDK5/CDK7 and treating carcinoma, melanoma, leukemia, intestine cancer, ovarian cancer, bladder cancer, pancreatic cancer, gastric cancer, stomach cancer, breast cancer, prostate cancer, does not reasonably provide enablement for treating autoimmune diseases, infectious diseases, inflammatory diseases, proliferative diseases other than carcinoma, melanoma, leukemia, intestine cancer, ovarian cancer, bladder cancer, pancreatic cancer, gastric cancer, stomach cancer, breast cancer, prostate 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 autoimmune diseases, infectious diseases, inflammatory diseases, proliferative diseases, said method comprising administration of the compound or pharmaceutically acceptable salt thereof according to claim 1. The state of the prior art: The state of the prior art: As indicated by the prior art, there is not any association between CDK5/CDK7 inhibitors and treating autoimmune diseases, infectious diseases, inflammatory diseases, proliferative diseases other than carcinoma, melanoma, leukemia, intestine cancer, ovarian cancer, bladder cancer, pancreatic cancer, gastric cancer, stomach cancer, breast cancer, prostate cancer. There is no guidance in the prior art that CDK5/CDK7 inhibitor could be useful to treat autoimmune diseases, infectious diseases, inflammatory diseases, proliferative diseases other than carcinoma, melanoma, leukemia, intestine cancer, ovarian cancer, bladder cancer, pancreatic cancer, gastric cancer, stomach cancer, breast cancer, prostate cancer. The predictability in the art: At present using CDK5/CDK7 to treat autoimmune diseases, infectious diseases, inflammatory diseases, proliferative diseases other than carcinoma, melanoma, leukemia, intestine cancer, ovarian cancer, bladder cancer, pancreatic cancer, gastric cancer, stomach cancer, breast cancer, prostate cancer is purely speculative. It is noted that the 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 CDK5/CDK7 on pages 89-100. However, there is no guidance for using a therapeutically effective amount of a compound of Formula (I) to treat autoimmune diseases, infectious diseases, inflammatory diseases, proliferative diseases other than carcinoma, melanoma, leukemia, intestine cancer, ovarian cancer, bladder cancer, pancreatic cancer, gastric cancer, stomach cancer, breast cancer, prostate cancer. The breadth of the claims: The claims encompass a method for treating autoimmune diseases, infectious diseases, inflammatory diseases, proliferative diseases. 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 21-27, for treating diseases associated with therapeutically effective amount of a compound of Formula (I) is efficacious, have been enabled by the instant specification. 3. Claims 21-27 are rejected under 35 U.S.C. 112, first paragraph, because the specification, does not reasonably provide enablement for preventing autoimmune diseases, infectious diseases, inflammatory diseases, proliferative diseases. The specification does not enable any person skilled in the art to which, or with which it is most nearly connected, to make and/or use the invention commensurate in scope with these claims. Applicants are not enabled for preventing any of these diseases. The only established prophylactics are vaccines not the compounds such as present here. In addition, it is presumed that “prevention” of the claimed diseases would require a method of identifying those individuals who will develop the claimed diseases before they exhibit symptoms. There is no evidence of record that would guide the skilled clinician to identify those who have the potential of becoming afflicted. “The factors to be considered [in making an enablement rejection] have been summarized as the quantity of experimentation necessary, the amount of direction or guidance presented, the presence or absence of working examples, the nature of the invention, the state of the prior art, the relative skill of those in that art, the predictability or unpredictability of the art, and the breadth of the claims”, In re Rainer, 146 USPQ 218 (1965); In re Colianni, 195 USPQ 150, Ex parte Formal, 230 USPQ 546. 1) As discussed above, preventing diseases requires identifying those patients who will acquire the disease before occurs. This would require extensive and potentially opened ended clinical research on healthy subjects. 2) The passage spanning line 31, page 39 to line 32, page 40 lists the diseases Applicant intend to treat. 3) There is no working example of such a preventive procedure in man or animal in the specification. 4) The claims rejected are drawn to medical treatment and are therefore physiological in nature. 5) The state of the art is that no general procedure is art-recognized for determining which patients generally will become afflicted before the fact. 6) The artisan using Applicants invention would be a Board Certified physician who specialized to treat diseases with an MD degree and several years of experience. Despite intensive efforts, pharmaceutical science has been unable to find a way of getting a compound to be effective for the prevention of disorder diseases generally. Under such circumstances, it is proper for the PTO to require evidence that such an unprecedented feat has actually been accomplished, In re Ferens, 163 USPQ 609. No such evidence has been presented in this case. The failure of skilled scientists to achieve a goal is substantial evidence that achieving such a goal is beyond the skill of practitioners in that art, Genentech vs. Novo Nordisk, 42 USPQ2nd 1001, 1006. This establishes that it is not reasonable to any agent to be able to prevent disorders generally. That is, the skill is so low that no compound effective generally against disorders has ever been found let alone one that can prevent such conditions. 7) It is well established that “the scope of enablement varies inversely with the degree of unpredictability of the factors involved", and physiological activity is generally considered to be an unpredictable factor. See In re Fisher, 427 F.2d 833, 839, 166 USPQ 18, 24 (CCPA 1970). 8) The claims broadly read on all patients, not just those undergoing therapy for the claimed diseases and on the multitude of compounds embraced by Formula (I). The Examiner suggests deletion of the word “prevention”. 4. Claim Rejections - 35 USC § 112 The following is a quotation of the second paragraph of 35 U.S.C. 112: The specification shall conclude with one or more claims particularly pointing out and distinctly claiming the subject matter which the applicant regards as his invention. Claims 1-27 are rejected under 35 U.S.C. 112, second paragraph, as being indefinite for failing to particularly point out and distinctly claim the subject matter which applicant regards as the invention. Claims 1-27 are rejected because the term “E3 ubiquitin binding group” is confusing. What is “E3 ubiquitin binding group”? It is very broad. There are no meets and bounds for “E3 ubiquitin binding group”. Examiner suggest to provide specific “E3 ubiquitin binding group”. Correction is required. 5. 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 1-27 are provisional rejected under the judicially created doctrine obviousness-type double patenting as being unpatentable over the claims 1-30, 35-37 of ap# 18/848,272. 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 application. Determination of the scope and content of the prior art (MPEP §2141.01) Ap# ‘272 claimed analogues compounds in claims 1-30, 35-37 as the instant claims 1-27. Ascertainment of the difference between the prior art and the claims (MPEP §2141.02) The difference between the instant claims and the claims 1-30, 35-37 of ap# ‘272 is 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 the 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. This is provisional obviousness-type double patenting rejection because the conflicting claims have not in fact been issued. 6. Claims 1-27 are provisional rejected under the judicially created doctrine obviousness-type double patenting as being unpatentable over the claims 1-9, 11-20 of ap# 18/036,102. 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 application. Determination of the scope and content of the prior art (MPEP §2141.01) Ap# ‘102 claimed analogues compounds in claims 1-30, 35-37 as the instant claims 1-27. Ascertainment of the difference between the prior art and the claims (MPEP §2141.02) The difference between the instant claims and the claims 1-30, 35-37 of ap# ‘102 is 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 the 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. This is provisional obviousness-type double patenting rejection because the conflicting claims have not in fact been issued. 7. 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/ 01/21/2026
Read full office action

Prosecution Timeline

Nov 20, 2023
Application Filed
Jan 21, 2026
Non-Final Rejection — §112, §DP (current)

Precedent Cases

Applications granted by this same examiner with similar technology

Patent 12595249
ARYL ETHER-SUBSTITUTED HETEROCYCLIC COMPOUNDS AS GLP1R AGONISTS
2y 5m to grant Granted Apr 07, 2026
Patent 12582718
INTEGRIN TARGETING LIGANDS AND USES THEREOF
2y 5m to grant Granted Mar 24, 2026
Patent 12577242
PYRROLOPYRIDINE AND IMIDAZOPYRIDINE ANTIVIRAL COMPOUNDS
2y 5m to grant Granted Mar 17, 2026
Patent 12577245
SULFONYL BENZAMIDE DERIVATIVES AS BCL-2 INHIBITORS
2y 5m to grant Granted Mar 17, 2026
Patent 12570655
CYSTEINE COVALENT MODIFIERS OF AKT1 AND USES THEREOF
2y 5m to grant Granted Mar 10, 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

1-2
Expected OA Rounds
77%
Grant Probability
74%
With Interview (-2.9%)
2y 1m
Median Time to Grant
Low
PTA Risk
Based on 1128 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