Prosecution Insights
Last updated: August 06, 2026
Application No. 17/937,670

Antimicrobial Compounds and Methods of Use

Non-Final OA §102§DP
Filed
Oct 03, 2022
Priority
Jun 28, 2016 — provisional 62/355,825 +2 more
Examiner
MURESAN, ANA Z
Art Unit
1692
Tech Center
1600 — Biotechnology & Organic Chemistry
Assignee
Aequor Inc.
OA Round
3 (Non-Final)
75%
Grant Probability
Favorable
3-4
OA Rounds
0m
Est. Remaining
99%
With Interview

Examiner Intelligence

Grants 75% — above average
75%
Career Allowance Rate
542 granted / 723 resolved
+15.0% vs TC avg
Strong +32% interview lift
Without
With
+31.6%
Interview Lift
resolved cases with interview
Typical timeline
2y 3m
Avg Prosecution
33 currently pending
Career history
749
Total Applications
across all art units

Statute-Specific Performance

§101
1.3%
-38.7% vs TC avg
§103
40.8%
+0.8% vs TC avg
§102
17.1%
-22.9% vs TC avg
§112
28.1%
-11.9% vs TC avg
Black line = Tech Center average estimate • Based on career data from 723 resolved cases

Office Action

§102 §DP
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 . Request for continued examination 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and the fee set forth in 37 CFR 1.17(e) has been timely paid, the finality of the previous Office action has been withdrawn pursuant to 37 CFR 1.114.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 5/18/2026 has been entered. DETAILED ACTION As filed, claims 17-21, 24, 28, 32 are pending; of which, claim 17 is currently amended. Claims 1-16, 22, 23, 25-27, 29-31, 33 are canceled.Claims 20, 21, 28, 32 are withdrawn from further consideration.A complete response to this Office Action should include cancellation of non-elected subject matter or other appropriate action. Claims 17-19, 24 are examined herein. Rejections Withdrawn Applicant’s amendments have been fully considered and are entered. The status for each rejection and/or objection in the previous Office Action is set out below. 1. The rejection of claims 17-19, 24 under 35 U.S.C. § 112 second paragraph is withdrawn in view of claim amendments and per argument submitted by Applicants. Applicant's arguments (Remarks page 8) were carefully considered and were found persuasive. 2. The NSDP rejection of claims 17-19, 24 over claims 23, 24, 45 of copending Application No. 18248020 is maintained. A terminal disclaimer has not been submitted to overcome this rejection. Claim Rejections - 35 USC § 102 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. (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. (a)(2) the claimed invention was described in a patent issued under section 151, or in an application for patent published or deemed published under section 122(b), in which the patent or application, as the case may be, names another inventor and was effectively filed before the effective filing date of the claimed invention. 1. Claims 17, 18 and 24 are rejected under 35 U.S.C. 102 (a)(1) and 102(a)(2) as being anticipated by Atherton et al. Journal of the Chemical Society (1945) 660-3 (cited in PTO-892 attached herewith). The ‘article by Atherton teaches on experimental page 662-663 , the dialkyl phosphamide of di-benzyl phosphamide compounds of structure shown below which corresponds to the instantly claimed compounds of formula II wherein variable Y is O, X is NH2 (instant claim 18) and A is C1-10 hydrocarbyl (C2 alkyl, C3 alkyl or benzyl) and G is an C1-10 hydrocarbyl ( C2 alkyl, C3 alkyl or -benzyl). Shown below are the anticipatory compounds disclosed by the ‘516 patent as displayed in Registry file: RN 1068-21-9 CAPLUS CN Phosphoramidic acid, diethyl ester (CA INDEX NAME) PNG media_image1.png 114 228 media_image1.png Greyscale RN 3905-76-8 CAPLUS CN Phosphoramidic acid, bis(phenylmethyl) ester (CA INDEX NAME) PNG media_image2.png 164 371 media_image2.png Greyscale RN 6415-20-9 CAPLUS CN Phosphoramidic acid, bis(1-methylethyl) ester (CA INDEX NAME) PNG media_image3.png 114 228 media_image3.png Greyscale Regarding instant claim 24, the prior art teaches composition of the compounds in solvent (preparative examples on page 663). Since the compounds disclosed in the prior art has the same structure as the instantly claimed compound, each and every required element of the claim is taught and the claim is anticipated. 2.Claims 17, 18 are rejected under 35 U.S.C. 102 (a)(1) and 102(a)(2) as being anticipated by CAS Registry STN Substance Record for 1361416-64-9 Entered STN: 21 Mar 2012 (cited in PTO-892 attached herewith). CAS Registry RN 1361416-64-9 discloses the compound of structure shown below which corresponds to the instantly claimed compounds of formula II wherein variable Y is O, X is NH2 (instant claim 18) and A is C1-10 hydrocarbyl (C2-alkyl) and G is an C4 alkenyl group. Shown below is the anticipatory compound as displayed in Registry file: RN 1361416-64-9 CAPLUS CN Phosphoramidic acid, 3-buten-1-yl ethyl ester (CA INDEX NAME) PNG media_image4.png 110 293 media_image4.png Greyscale Therefore, the prior art teaches the limitations of instant claims. 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. 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 § 2146 et seq. 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 filing of a terminal disclaimer by itself is not a complete reply to a nonstatutory double patenting (NSDP) rejection. A complete reply requires that the terminal disclaimer be accompanied by a reply requesting reconsideration of the prior Office action. Even where the NSDP rejection is provisional the reply must be complete. See MPEP § 804, subsection I.B.1. For a reply to a non-final Office action, see 37 CFR 1.111(a). For a reply to final Office action, see 37 CFR 1.113(c). A request for reconsideration while not provided for in 37 CFR 1.113(c) may be filed after final for consideration. See MPEP §§ 706.07(e) and 714.13. The USPTO Internet website contains terminal disclaimer forms which may be used. Please visit www.uspto.gov/patent/patents-forms. The actual 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/apply/applying-online/eterminal-disclaimer. Claims 17-19, 24 are provisionally rejected on the ground of nonstatutory double patenting as being unpatentable over claims 23, 24, 45 of copending Application No. 18248020. Although the claims at issue are not identical, they are not patentably distinct from each other because they are drawn to a substantial amount of overlapping subject matter. The elected species is recited in claim 45 of the ‘020 application. This is a provisional nonstatutory double patenting rejection because the patentably indistinct claims have not in fact been patented. Relevant Prior Art The prior art made of record and not relied upon is considered pertinent to applicant's disclosure: AN 1981:46741 CAPLUS Full-text DN 94:46741 OREF 94:7613a,7616a TI Investigation on products of reaction of O,O-dialkyl phosphoramidates with sulfonyl diisocyanate. Part II AU Arnold, Zdzislaw CS Physiol.-Biochem. Inst., Mil. Sch. Med., Lodz, 90647, Pol. SO Polish Journal of Chemistry (1980), 54(4), 703-7 CODEN: PJCHDQ; ISSN: 0137-5083 DT Journal LA English OS CASREACT 94:46741 AB The addn. of (RO)2P(O)NH2 (R = Et, Pr, Me2CH, Bu, Me2CHCH2) with OCNSO2NCO gave (RO)2P(O)NHCONHSO2NHCONHP(O)(OR)2 (same R). IT 870-52-0 1068-21-9 6415-20-9 17123-09-0 56477-39-5 RL: RCT (Reactant); RACT (Reactant or reagent) (addn. reaction of, with sulfonyl diisocyanate) RN 870-52-0 CAPLUS CN Phosphoramidic acid, dibutyl ester (CA INDEX NAME) PNG media_image5.png 114 358 media_image5.png Greyscale RN 1068-21-9 CAPLUS CN Phosphoramidic acid, diethyl ester (CA INDEX NAME) PNG media_image1.png 114 228 media_image1.png Greyscale RN 6415-20-9 CAPLUS CN Phosphoramidic acid, bis(1-methylethyl) ester (CA INDEX NAME) PNG media_image3.png 114 228 media_image3.png Greyscale RN 17123-09-0 CAPLUS CN Phosphoramidic acid, dipropyl ester (CA INDEX NAME) PNG media_image6.png 114 293 media_image6.png Greyscale RN 56477-39-5 CAPLUS CN Phosphoramidic acid, bis(2-methylpropyl) ester (CA INDEX NAME) PNG media_image7.png 145 293 media_image7.png Greyscale 2. AN 1980:76858 CAPLUS Full-text DN 92:76858 OREF 92:12679a,12682a TI I. Studies of 2,2'-bipyridyl-N,N'-dioxides. II. A potential approach to polynucleotide synthesis. III. Novel eight-membered ring C,N,S-compounds AU Wenkert, David CS Harvard Univ., Cambridge, MA, USA SO (1979) 228 pp. Avail.: Univ. Microfilms Int., Order No. 7922244 From: Diss. Abstr. Int. B 1979, 40(4), 1728 DT Dissertation LA English OS CASREACT 92:76858 AB Unavailable IT 1361416-57-0P 1361416-64-9P 1361416-71-8P RL: RCT (Reactant); SPN (Synthetic preparation); PREP (Preparation); RACT (Reactant or reagent) (prepn. of a phosphonating reagent for oligonucleotide synthesis) RN 1361416-57-0 CAPLUS CN Propanoic acid, 3-[(aminoethoxyphosphinyl)oxy]-, phenylmethyl ester (CA INDEX NAME) PNG media_image8.png 153 424 media_image8.png Greyscale RN 1361416-64-9 CAPLUS CN Phosphoramidic acid, 3-buten-1-yl ethyl ester (CA INDEX NAME) PNG media_image4.png 110 293 media_image4.png Greyscale RN 1361416-71-8 CAPLUS CN Phosphoramidic acid, ethyl 3-hydroxypropyl ester (CA INDEX NAME) PNG media_image9.png 110 310 media_image9.png Greyscale IT 195141-03-8P 1361416-56-9P RL: SPN (Synthetic preparation); PREP (Preparation) (prepn. of a phosphonating reagent for oligonucleotide synthesis) RN 195141-03-8 CAPLUS CN Phosphoramidic acid, ethyl 3-(phenylmethoxy)propyl ester (CA INDEX NAME) PNG media_image10.png 148 424 media_image10.png Greyscale RN 1361416-56-9 CAPLUS CN Propanoic acid, 3-[(aminoethoxyphosphinyl)oxy]- (CA INDEX NAME) PNG media_image11.png 115 310 media_image11.png Greyscale AN 1979:507655 CAPLUS Full-text DN 91:107655 OREF 91:17367a,17370a TI N-Phosphorylated formamidines IN Guenther, Eberhard; Kochmann, Werner; Luthardt, Horst; Naumann, Kurt; Roethling, Tilo PA VEB Chemiekombinat Bitterfeld, Ger. Dem. Rep. SO Ger. (East), 7 pp. CODEN: GEXXA8 DT Patent LA German FAN.CNT 1 PI PATENT NO. KIND DATE APPLICATION NO. DATE --------------- ---- -------- --------------------- -------- DD 134872 A1 19790328 DD 1978-204026 19780308 PRAI DD 1978-204026 A1 19780308 PSPI PATENT NO. KIND STATUS STATUS DATE --------------- ---- ------------- ----------- DD 134872 A1 Dead 20201107 AB Reaction of (RX)(RO)P(Y)NH2 (X, Y = O or S, R = C1-12 alkyl) with DMF (promoted by SOCl2 or COCl2) gave 70-90% (RX)(RO)P(Y)NiCHNMe2 (X = O, Y = S, R = Et, X = Y = O, R = Et, Pr, Me2CH, Bu, Me2CHCH2, EtCHMeCH2, BuCHMeCH2, n-C10H21). IT 870-52-0 1068-21-9 6415-20-9 RL: RCT (Reactant); RACT (Reactant or reagent) (reaction of, with DMF) RN 870-52-0 CAPLUS CN Phosphoramidic acid, dibutyl ester (CA INDEX NAME) PNG media_image5.png 114 358 media_image5.png Greyscale RN 1068-21-9 CAPLUS CN Phosphoramidic acid, diethyl ester (CA INDEX NAME) PNG media_image1.png 114 228 media_image1.png Greyscale RN 6415-20-9 CAPLUS CN Phosphoramidic acid, bis(1-methylethyl) ester (CA INDEX NAME) PNG media_image3.png 114 228 media_image3.png Greyscale --------------- ---- -------- --------------------- -------- US 3761545 A 19730925 US 1971-165581 19710723 PRAI US 1971-165581 A 19710723 PSPI PATENT NO. KIND STATUS STATUS DATE --------------- ---- ------------- ----------- US 3761545 A Dead 20201106 AB (BuCHEtCH2O)2P(O)NH2 was prepd. by refluxing a mixt. of (BuCHEtCH2O)2P(O)OH and urea in MePh. A mixt. of mono- and diisooctyl phosphates reacted similarly and the reaction was claimed for alkyl pyrophosphates. IT 13024-82-3P RL: SPN (Synthetic preparation); PREP (Preparation) (prepn. of) RN 13024-82-3 CAPLUS CN Phosphoramidic acid, bis(2-ethylhexyl) ester (CA INDEX NAME) PNG media_image12.png 184 488 media_image12.png Greyscale Conclusion Claims 17-19, 24 are rejected. Claims 20, 21, 22-23, 25, 28-29, 32-33 are withdrawn from further consideration. Telephone Inquiry Any inquiry concerning this communication or earlier communications from the examiner should be directed to ANA MURESAN whose telephone number is (571)-270-7587. The examiner can normally be reached on Monday through Friday, 8:30 am to 5:30 pm EAST. If attempts to reach the examiner by telephone are unsuccessful, the examiner’s supervisor, Robert Havlin can be reached at 571-272-9066. 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. /ANA Z MURESAN/Primary Examiner, Art Unit 1692
Read full office action

Prosecution Timeline

Show 2 earlier events
Sep 26, 2025
Response Filed
Dec 18, 2025
Final Rejection mailed — §102, §DP
May 01, 2026
Interview Requested
May 07, 2026
Applicant Interview (Telephonic)
May 07, 2026
Examiner Interview Summary
May 18, 2026
Request for Continued Examination
May 19, 2026
Response after Non-Final Action
Jun 02, 2026
Non-Final Rejection mailed — §102, §DP (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

3-4
Expected OA Rounds
75%
Grant Probability
99%
With Interview (+31.6%)
2y 3m (~0m remaining)
Median Time to Grant
High
PTA Risk
Based on 723 resolved cases by this examiner. Grant probability derived from career allowance rate.

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