Prosecution Insights
Last updated: July 17, 2026
Application No. 18/632,254

DEUTERATED NUCLEOSIDE COMPOUNDS AND USE THEREOF

Non-Final OA §103§112
Filed
Apr 10, 2024
Priority
May 17, 2022 — CN 202210548373.7 +5 more
Examiner
OH, TAYLOR V
Art Unit
1625
Tech Center
1600 — Biotechnology & Organic Chemistry
Assignee
Guizhou Bailing Group Pharmaceutical Co. Ltd.
OA Round
1 (Non-Final)
81%
Grant Probability
Favorable
1-2
OA Rounds
0m
Est. Remaining
97%
With Interview

Examiner Intelligence

Grants 81% — above average
81%
Career Allowance Rate
1428 granted / 1760 resolved
+21.1% vs TC avg
Strong +16% interview lift
Without
With
+15.5%
Interview Lift
resolved cases with interview
Typical timeline
2y 3m
Avg Prosecution
43 currently pending
Career history
1788
Total Applications
across all art units

Statute-Specific Performance

§101
0.7%
-39.3% vs TC avg
§103
61.6%
+21.6% vs TC avg
§102
15.6%
-24.4% vs TC avg
§112
16.8%
-23.2% vs TC avg
Black line = Tech Center average estimate • Based on career data from 1760 resolved cases

Office Action

§103 §112
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 . Non-Final Rejection The Status of Claims: Claims 1-7 are pending. Claims 1, 4-5 and 7 are rejected. Claims 2-3 are objected. Claim 6 is allowable. DETAILED ACTION 1. Claims 1-7 are under consideration in this Office Action. Priority 2. It is noted that this application is a continuation of 18682091 02/07/2024 ,which is is a 371 of PCT/CN2023/094871 05/17/2023 , which has a foreign priority documents, CHINA CN202210548373.7 05/17/2022; CHINA CN202210695557.6 06/15/2022; CHINA CN202211002496.7 08/19/2022 ; and CHINA CN202310213459.9 03/07/2023. Drawings 3. None. IDS 4. The IDS filed on 10/02/2024 are reviewed by the examiner. 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 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 Objections Claims 2-3 are 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. Claim Rejections - 35 USC § 112 The following is a quotation of 35 U.S.C. 112(b): (b) CONCLUSION.—The specification shall conclude with one or more claims particularly pointing out and distinctly claiming the subject matter which the inventor or a joint inventor regards as the invention. The following is a quotation of 35 U.S.C. 112 (pre-AIA ), second paragraph: 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. Claim 7 is rejected under 35 U.S.C. 112(b) or 35 U.S.C. 112 (pre-AIA ), second paragraph, as being indefinite for failing to particularly point out and distinctly claim the subject matter which the inventor or a joint inventor (or for applications subject to pre-AIA 35 U.S.C. 112, the applicant), regards as the invention. In claim 7, the phrase” treating diseases related to RNA-dependent RNA polymerase inhibitor “ is recited. This expression can be vague and indefinite because the claim does not explain how the diseases are related to RNA-dependent RNA polymerase inhibitor in the claim. The examiner recommends to put the specific names for the diseases related to RNA-dependent RNA polymerase inhibitor in the claim Claim Rejections - 35 USC § 103 This application currently names joint inventors. In considering patentability of the claims the examiner presumes that the subject matter of the various claims was commonly owned as of the effective filing date of the claimed invention(s) absent any evidence to the contrary. Applicant is advised of the obligation under 37 CFR 1.56 to point out the inventor and effective filing dates of each claim that was not commonly owned as of the effective filing date of the later invention in order for the examiner to consider the applicability of 35 U.S.C. 102(b)(2)(C) for any potential 35 U.S.C. 102(a)(2) prior art against the later invention. 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 of this title, 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. The text of those sections of Title 35, U.S. Code not included in this action can be found in a prior Office action. The factual inquiries set forth in Graham v. John Deere Co., 383 U.S. 1, 148 USPQ 459 (1966), that are applied for establishing a background for determining obviousness under 35 U.S.C. 103 are summarized as follows: 1. Determining the scope and contents of the prior art. 2. Ascertaining the differences between the prior art and the claims at issue. 3. Resolving the level of ordinary skill in the pertinent art. 4. Considering objective evidence present in the application indicating obviousness or nonobviousness. 5. Claims 1, and 4-5 are rejected under 35 U.S.C. 103 as being unpatentableover Zhang et al et al (US2024/0317754 A1) , which is equivalent to Zhang et al et al (CN 113735862). Applicant claims the followings: 1. A compound of formula (VI-1), a stereoisomer thereof, or a pharmaceutically acceptable salt thereof, PNG media_image1.png 238 370 media_image1.png Greyscale PNG media_image2.png 64 230 media_image2.png Greyscale ; wherein R2 and R3 are each independently selected from hydrogen, C1-6 alkyl-C(=O)-, C1-4 alkoxy-C(=O)-, and phenyl-C(=O)-, and the C1-6 alkyl, C1-4 alkoxy, and phenyl are each independently and optionally substituted by 1, 2, or 3 R; R5 is selected from phenyl, and the phenyl is optionally substituted by 1, 2, or 3 R; each R is independently selected from hydroxyl, halogen, amino, and cyano. PNG media_image2.png 64 230 media_image2.png Greyscale . 4. The compound, the stereoisomer thereof, or the pharmaceutically acceptable salt thereof according to claim 1, wherein R2 and R3 are each independently selected from hydrogen, isopropyl-C(=O)-, and phenyl-C(=O)-, and the isopropyl and phenyl are each independently and optionally substituted by 1, 2, or 3 R. 5. The compound, the stereoisomer thereof, or the pharmaceutically acceptable salt thereof according to claim 4, wherein R2 and R3 are each independently selected from hydrogen, isopropyl-C(=O)-, and . PNG media_image3.png 100 96 media_image3.png Greyscale . Determination of the scope and content of the prior art Zhang et al discloses the following compound with an anti-viral activity: PNG media_image4.png 355 346 media_image4.png Greyscale (see page 27, a paragraph##0220, compound# ATV13). The current invention, however, differs from the prior art in that the deuterium atom being connected to furan in the claimed compound is unspecified in the prior art. Ascertainment of the difference between the prior art and the claims The difference between the instant application and the applied Zhang et al Cowen art is that the Zhang et al does not expressly teach the claimed deuterium atom being connected to furan in the claimed compound. Resolving the level of ordinary skill in the pertinent art. Regarding the Claims 1 and 4-5, with respect to the lack of disclosing the claimed deuterium atom being connected to furan in the claimed compound, the prior art is silent about it. However, those skilled in the art know that deuterium atom is an isotope atom of hydrogen atom, which has similar chemical properties, and the prior art provides a technical motivation that the hydrogen atom can be replaced by a deuterium atom ( see page 37, the general formula of claim 1 ). Thus, in order to obtain a series of compounds with antiviral activity, the skilled artisan in the art is motivated to replace hydrogen atoms with deuterium atoms on the basis of existing technology. So, if the skilled artisan in the art had desired to test a particular compound having deuterium atom being connected to furan in the Zhang’s compound as an alternative, it would have been obvious to the skilled artisan in the art before the effective filing date of the claimed invention to be motivated to form the compound and evaluate its antiviral activity. This is because the skilled artisan in the art would expect such a procedure to be feasible and successful as guidance shown the prior art. Considering objective evidence present in the application indicating obviousness or nonobviousness. Zhang et al expressly discloses the following compound with an anti-viral activity: PNG media_image4.png 355 346 media_image4.png Greyscale . Although the Zhang et al does not teach the claimed deuterium atom being connected to furan in the claimed compound, the prior art does specify indirectly that a deuterium can be substituted for any variable of R7 and R8 in the formula (I) (see page 37, claim 1). Not only this information, but also, it is well-known knowledge in the art that deuterium atom is an isotope atom of hydrogen atom, which has similar chemical properties. Thus, in order to obtain a series of compounds with antiviral activity, the skilled artisan in the art is motivated to replace hydrogen atoms with deuterium atoms on the basis of existing technology. So, if the skilled artisan in the art had desired to test a particular compound having deuterium atom being connected to furan in the Zhang’s compound as an alternative, it would have been obvious to the skilled artisan in the art before the effective filing date of the claimed invention to be motivated to form the compound and evaluate its antiviral activity. This is because the skilled artisan in the art would expect such a procedure to be feasible and successful as guidance shown the prior art. Conclusion Claims 1, 4-5 and 7 are rejected. Claims 2-3 are objected. Claim 6 is allowable. Any inquiry concerning this communication or earlier communications from the examiner should be directed to TAYLOR V OH whose telephone number is (571)272-0689. The examiner can normally be reached on 8:00-5:00. 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, Anna Jiang can be reached on 571-272-0627. The fax phone number for the organization where this application or proceeding is assigned is 571-273-8300. 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). If you would like assistance from a USPTO Customer Service Representative or access to the automated information system, call 800-786-9199 (IN USA OR CANADA) or 571-272-1000. /TAYLOR V OH/Primary Examiner, Art Unit 1625 5/29/2026
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Prosecution Timeline

Apr 10, 2024
Application Filed
Jun 03, 2026
Non-Final Rejection mailed — §103, §112 (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
81%
Grant Probability
97%
With Interview (+15.5%)
2y 3m (~0m remaining)
Median Time to Grant
Low
PTA Risk
Based on 1760 resolved cases by this examiner. Grant probability derived from career allowance rate.

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