Prosecution Insights
Last updated: April 18, 2026
Application No. 18/563,327

HARD-SHELL CAPSULE WITH INFLUX PREVENTION OF GASTRIC FLUIDS

Non-Final OA §103§112§DP
Filed
Nov 21, 2023
Examiner
MERCIER, MELISSA S
Art Unit
1615
Tech Center
1600 — Biotechnology & Organic Chemistry
Assignee
Evonik Operations GmbH
OA Round
1 (Non-Final)
72%
Grant Probability
Favorable
1-2
OA Rounds
2y 9m
To Grant
79%
With Interview

Examiner Intelligence

Grants 72% — above average
72%
Career Allow Rate
852 granted / 1181 resolved
+12.1% vs TC avg
Moderate +7% lift
Without
With
+6.9%
Interview Lift
resolved cases with interview
Typical timeline
2y 9m
Avg Prosecution
50 currently pending
Career history
1231
Total Applications
across all art units

Statute-Specific Performance

§101
1.1%
-38.9% vs TC avg
§103
41.2%
+1.2% vs TC avg
§102
17.1%
-22.9% vs TC avg
§112
25.3%
-14.7% vs TC avg
Black line = Tech Center average estimate • Based on career data from 1181 resolved cases

Office Action

§103 §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 . Status of Application Receipt of the Preliminary Amendments dated November 21, 2023 and December 4, 2023 is acknowledged. Claims 1-16 are pending in this application. Claims 1-15 have been amended. Claim 16 is new. All pending claims are under examination in this application. Information Disclosure Statement Receipt of the Information Disclosure Statements filed on November 21, 2023; December 5, 2023; and June 14, 2024 is acknowledged. A signed copy is attached to this office action. 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. Claims 1-16 are 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. Claims 1-16 recite “a first coating solution, suspension, or dispersion comprising or consisting of..” in line 9 and “a second coating solution, suspension, or dispersion comprising or consisting of...” in lines 18-19. Applicant has not particularly pointed out what the coating layers are limited to. It is unclear what is excluded/included in the claim based on the comprising/consisting of language. For purposes of prosecution in application of prior art, the claims are being examined utilizing “comprising”. The claims must be limited to one transition phrase. Regarding claim 11, the claim recites “the process according to claim 1, wherein up to 400 % by weight, based on the total weight of the at least one polymer, and of the at least one additive are comprised in the first and/or second coating solution, suspension or dispersion”. It is unclear how the polymer and additive component can be 400% of the first and/or second coating. Clarification is requested. Claim Rejections - 35 USC § 103 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, 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 factual inquiries 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. 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. Claims 1-16 are rejected under 35 U.S.C. 103 as being obvious over Guha et al. (WO 2019/096833, cited on IDS dated 11-21-2023) in view of Roy et al. (Effect of plasticizers and surfactants on the film forming properties of hydroxypropyl methylcellulose for the coating of diclofenac sodium tablets, Saudi Pharmaceutical Journal (2009) 17, 233-241). The applied reference has a common assignee and inventor with the instant application. Based upon the earlier effectively filed date of the reference, it constitutes prior art under 35 U.S.C. 102(a)(2). This rejection under 35 U.S.C. 103 might be overcome by: (1) a showing under 37 CFR 1.130(a) that the subject matter disclosed in the reference was obtained directly or indirectly from the inventor or a joint inventor of this application and is thus not prior art in accordance with 35 U.S.C.102(b)(2)(A); (2) a showing under 37 CFR 1.130(b) of a prior public disclosure under 35 U.S.C. 102(b)(2)(B); or (3) a statement pursuant to 35 U.S.C. 102(b)(2)(C) establishing that, not later than the effective filing date of the claimed invention, the subject matter disclosed and the claimed invention were either owned by the same person or subject to an obligation of assignment to the same person or subject to a joint research agreement. See generally MPEP § 717.02. Guha discloses a process for preparing a polymer-coated hard shell capsule, suitable as container for pharmaceutical or nutraceutical biologically active ingredients, wherein the hard shell capsule is comprising a body and a cap, wherein in the closed state the cap overlaps the body either in a pre-locked state or in a final-locked state, wherein the hard shell capsule is provided in the pre-locked state and spray-coated with a coating solution, suspension or dispersion comprising a polymer or a mixture of polymers to create a coating layer which covers the outer surface of the hard shell capsule in the pre-locked state (abstract). The polymer or polymer mixture comprised in the coating layer are preferably film-forming polymers and may be selected from the groups of anionic polymers, cationic polymers and neutral polymers or any mixtures thereof (page 10, lines 33-35). The coating layer can optionally comprise excipient (page 18, lines 28-30). Suitable excipients include plasticizers, fillers, glidants, and pigments (page 23-25). The hard shell capsules many additionally contain a top coat. The top coat comprises a water soluble polymer such as a polysaccharide or hydroxypropyl methyl cellulose (HPMC), as well as optional excipients (page 25, lines 10-30). The coating amount can be from about 1 to about 8 mg/cm2 (page 17, lines 21-22). The top coating does not need to be applied in the pre lock state (page 25, lines 11-30), however, there is not direct teaching of it not being applied in the pre lock state. The top coating may have the function of coloring the pharmaceutical form or protecting from environmental influences (page 25, line 21-23). Regarding claim 2, the material of the body and cap may be selected from the HPMC, starch, gelatin, pullulan and a copolymer of C1- to C4-alkylester of (meth)acrylic acid and (meth)acrylic acid (page 9, lines 25-28). Regarding claim 3, the polymer or polymer matrix can comprise anionic (meth) acrylate copolymers (page 10, lines 10-12). Regarding claims 4 and 6, suitable anionic (meth)acrylate copolymers are those polymerized from of 40 to 60% by weight methacrylic acid and 60 to 40% by weight methyl methacrylate or 60 to 40% by weight ethyl acrylate (page 11, lines 18-20), for example. Regarding claim 5, Example 2 discloses the use of Eudragit FS30D and Eudragit L30D-55 which meets the limitation of ii. Regarding claim 7, suitable polymers for the coating include natural celluloses such as methyl, ethyl, and propyl ethers of celluloses, for example hydropropyl cellulose, polyvinyl pyrrolidone, polyvinyl acetate, and polyvinyl alcohol (page 17, lines 10-13). Regarding claim 8, as noted above, glidants can added. Regarding claim 9-10, the coating layer excipients can include glidants, emulsifiers, plasticizers, and flow agents, fragrances, pigments, flavoring agents, flow aids, or stabilizers (page 23, line 7-12), which would be addition additives. Regarding claim 11, the polymer is recited as the only required component and would therefore comprise 100% of the coating, which reads on the up to 400% recited in the claim. Regarding claim 12, it is disclosed the body and the cap are comprising encircling notches or dimples in the area where the cap overlaps the body, that allow the capsule to be closed by a snap-into-place mechanism either in the pre-locked state or in the final-locked state (claim 11). Regarding claim 13, the body of the capsule comprises a tapered rim (claim 12). Regarding claim 14, following the method of instant claim 1 results in a polymer coated hard shell capsule. Regarding claim 15, the capsule can be used to administer an active pharmaceutical agent within the capsule. The recitation of immediate, delayed, or sustained would encompass all release profiles of capsules. Regarding claim 16, as noted above, the top coating can comprise HPMC. While Guha discloses a top coating can be applied to the capsule, he does not disclose the coating comprises a solution, suspension, or dispersion comprising a least one polymer, at least one emulsifier, and at least one plasticizer, as well as optional components. Roy discloses top coats for pharmaceutical tablets. It is the position of the Examiner that coating tablets and capsules solves the same problem. The use of plasticizers is to ensure spreading and/or film forming capability. The type and concentration of plasticizers can affect the film properties (Introduction). Roy discloses plasticizers have a significant effect on the film forming properties of HPMC, being free from major defects like cracking, orange peel, and cracking with good gloss and slight chipping, thus inferring that plasticizers significantly influence that quality of the aqueous film coating. The addition of surfactants (emulsifiers) resulted in bringing uniformity in the spreading efficiency on the substrate surface. It was also determined that use of plasticizers and surfactants resulted in proper erosion and diffusion mechanisms to be operative during drug release from the optimized batch (Results and Discussion). It would have been obvious to one of ordinary skill in the part prior to the effective filing date of the invention to have included a plasticizer and an emulsifier as the excipients into the top coating of Guha in order to obtain the properties disclosed by Roy. 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 1-16 are rejected on the ground of nonstatutory double patenting as being unpatentable over claims 1-8 of U.S. Patent No. 11,980,692; claims 1-14 of U.S. Patent 11,523,992, and claims 1-20 of U.S. Patent No. 12,192,993. Although the claims at issue are not identical, they are not patentably distinct from each other because the instant claims and the patented claims are drawn to processes of preparing a polymer coated hard capsule shell utilizing the same polymeric coating. Claims 1-16 are provisionally rejected on the ground of nonstatutory double patenting as being unpatentable over claims 1-16 of copending Application No. 18/563,517. Although the claims at issue are not identical, they are not patentably distinct from each other because the instant claims and the copending claims are drawn to processes of preparing a polymer coated hard capsule shell utilizing the same polymeric coating. This is a provisional nonstatutory double patenting rejection because the patentably indistinct claims have not in fact been patented. Conclusion Any inquiry concerning this communication or earlier communications from the examiner should be directed to MELISSA S MERCIER whose telephone number is (571)272-9039. The examiner can normally be reached M-F 6:30 am to 4 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, Robert A Wax can be reached at 571-272-0623. 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. /MELISSA S MERCIER/Primary Examiner, Art Unit 1615
Read full office action

Prosecution Timeline

Nov 21, 2023
Application Filed
Apr 07, 2026
Non-Final Rejection — §103, §112, §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

1-2
Expected OA Rounds
72%
Grant Probability
79%
With Interview (+6.9%)
2y 9m
Median Time to Grant
Low
PTA Risk
Based on 1181 resolved cases by this examiner. Grant probability derived from career allow rate.

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