Prosecution Insights
Last updated: August 15, 2026
Application No. 19/218,926

SYSTEMS AND METHODS FOR GENERATING A NOCICEPTION NOURISHEMENT PROGRAM

Non-Final OA §103
Filed
May 27, 2025
Priority
Jul 24, 2023 — continuation of 12/334,208
Examiner
NGUYEN, HIEP VAN
Art Unit
Tech Center
Assignee
KPN Innovations LLC
OA Round
1 (Non-Final)
55%
Grant Probability
Moderate
1-2
OA Rounds
2y 8m
Est. Remaining
85%
With Interview

Examiner Intelligence

Grants 55% of resolved cases
55%
Career Allowance Rate
571 granted / 1035 resolved
-4.8% vs TC avg
Strong +30% interview lift
Without
With
+29.5%
Interview Lift
resolved cases with interview
Typical timeline
3y 11m
Avg Prosecution
38 currently pending
Career history
1080
Total Applications
across all art units

Statute-Specific Performance

§101
29.5%
-10.5% vs TC avg
§103
46.9%
+6.9% vs TC avg
§102
7.0%
-33.0% vs TC avg
§112
10.1%
-29.9% vs TC avg
Black line = Tech Center average estimate • Based on career data from 1035 resolved cases

Office Action

§103
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 Claims 21-36 have been examined. Claims 1-20, have been has been cancelled. 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 USPTO Internet website contains terminal disclaimer forms which may be used. Please visit www.uspto.gov/patent/patents-forms. The 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/process/file/efs/guidance/eTD-info-I.jsp. Claims 21, 36 are rejected on the ground of nonstatutory double patenting as being unpatentable over claims 1, 9 of U.S. Patent No. 11742069 and claims 1, 10 of US patent No. 12334210. Although the claims at issue are not identical, they are not patentably distinct from each other because both claims recite the same feature of retrieve a nociception parameter associated with a subject; classify the nociception parameter to a nociception grouping generate a nociception nourishment program as a function of the plurality of nutrition elements, wherein generating the nociception nourishment program comprises generating a nociception nourishment index. Allowable Subject Matter The primary reason for indicating allowability over the prior art is the inclusions of the following limitations in the combination as recited. Claim 21 is directed towards a system for tracking pain management from a nourishment program for nociception disorders, the system comprising: a computing device, wherein the computing device is configured to: retrieve a nociception parameter associated with a subject; identify a nociception biologic data associated with the nociception parameter; generate, a non-medicated treatment plan as a function of the nociception biologic data; and generate a nociception nourishment program as a function of the nociception biologic data, wherein generating the nociception nourishment program comprises generating a nociception nourishment index using an index model, wherein the index model comprises a machine learning module that is configured to: identify, by the machine learning module, pain state from the nociception biologic data; apply, by the machine learning module, a numerical assessment of pain management determined from the nociception parameter; generate, a nociception nourishment index as a function of pain state and the numerical assessment of pain management; and display, a subject's current nourishment and level of subject participation. For claim rejection under 35USC 101, the current invention recites “generate a nociception nourishment program as a function of the nociception biologic data, wherein generating the nociception nourishment program comprises generating a nociception nourishment index using an index model, wherein the index model comprises a machine learning module; identify, by the machine learning module, pain state from the nociception biologic data ”. Under Patent Subject Matter Eligibility Guidance (MPEP 2106.04-07), the combination of recited additional elements in the recited claims is patent eligible because the claims as a whole integrate an abstract idea into practical application under Prong Two of Step 2A of the Alice/Mayo Test. The claims are eligible because it is not directed to an abstract idea or any other judicial exception. For claim rejection under USC 103, the closet prior art relates to Zuckerman Starket al. (WO201706313A2 hereinafter Zuckerman) in view of Kane (US 20050177397). Zuckerman describes a nociception monitoring device including at least one sensor configured to sense at least three physiological parameters of a patient, and a computing unit configured to receive the at least three physiological parameters and to compute a nociception scale (NS) value, indicative of a nociception level of the patient, based on an analysis of the at least three physiological parameters. Kane describes linking consumers and nutritional pharmacologists offering personalized nutritional information through a central network site. However, both Zuckerman Stark and Kane fail to teach generating an indexing model using training data including a plurality of data entries correlating the respective effect of each nutrition element in the nociception nourishment program on the nociception parameter; and generating the nociception nourishment index as a function of the indexing model and the nutritional input. The NPL “Chronic Pain in Children and Adolescents: Diagnosis and Treatment of Primary Pain Disorders in Head, Abdomen, Muscles and Joints“ describes Primary pain disorders (formerly “functional pain syndromes”) are common, under-diagnosed and under-treated in children and teenagers. This manuscript reviews key aspects which support understanding the development of pediatric chronic pain, points to the current pediatric chronic pain terminology, addresses effective treatment strategies, and discusses the evidence-based use of pharmacology. Common symptoms of an underlying pain vulnerability present in the three most common chronic pain disorders in pediatrics: primary headaches, centrally mediated abdominal pain syndromes, and/or chronic/recurrent musculoskeletal and joint pain. However, the NPL of record does not disclose generating an indexing model using training data including a plurality of data entries correlating the respective effect of each nutrition element in the nociception nourishment program on the nociception parameter; and generating the nociception nourishment index as a function of the indexing model and the nutritional input. Claim 21-36 would be allowable if rewritten to overcome Double Patenting set forth in this Office action and to include all of the limitations of the base claim and any intervening claims. Conclusion Any inquiry concerning this communication or earlier communications from the examiner should be directed to HIEP VAN NGUYEN whose telephone number is (571)270-5211. The examiner can normally be reached Monday through Friday between 8:00AM and 5:00PM 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, Jason B Dunham can be reached on 5712728109. 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. /HIEP V NGUYEN/Primary Examiner, Art Unit 3686
Read full office action

Prosecution Timeline

May 27, 2025
Application Filed
Jul 29, 2026
Non-Final Rejection mailed — §103 (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
55%
Grant Probability
85%
With Interview (+29.5%)
3y 11m (~2y 8m remaining)
Median Time to Grant
Low
PTA Risk
Based on 1035 resolved cases by this examiner. Grant probability derived from career allowance rate.

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