Prosecution Insights
Last updated: April 19, 2026
Application No. 18/700,571

DEVICES AND METHODS FOR TREATING A VIRAL INFECTION AND SYMPTOMS THEREOF

Non-Final OA §DP
Filed
Apr 11, 2024
Examiner
MARCETICH, ADAM M
Art Unit
3781
Tech Center
3700 — Mechanical Engineering & Manufacturing
Assignee
Aethlon Medical Inc.
OA Round
1 (Non-Final)
72%
Grant Probability
Favorable
1-2
OA Rounds
3y 1m
To Grant
92%
With Interview

Examiner Intelligence

Grants 72% — above average
72%
Career Allow Rate
967 granted / 1336 resolved
+2.4% vs TC avg
Strong +20% interview lift
Without
With
+19.5%
Interview Lift
resolved cases with interview
Typical timeline
3y 1m
Avg Prosecution
43 currently pending
Career history
1379
Total Applications
across all art units

Statute-Specific Performance

§101
2.7%
-37.3% vs TC avg
§103
46.3%
+6.3% vs TC avg
§102
14.9%
-25.1% vs TC avg
§112
19.2%
-20.8% vs TC avg
Black line = Tech Center average estimate • Based on career data from 1336 resolved cases

Office Action

§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 . Claim Objections Claims 117-119 are omitted from the preliminary amendments filed 18 November 2024 and therefore have not been examined. Each amendment document that includes a change to an existing claim, including the deletion of an existing claim, or submission of a new claim, must include a complete listing of all claims ever presented (including previously canceled and non-entered claims) in the application. The current status of all of the claims in the application, including any previously canceled or withdrawn claims, must be given. Status is indicated in a parenthetical expression following the claim number by one of the following status identifiers: (original), (currently amended), (previously presented), (canceled), (withdrawn), (new), or (not entered). See MPEP 714(II)(C), Amendments to the 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 obviousness-type 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); and 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 a nonstatutory double patenting ground provided the conflicting application or patent either is shown to be commonly owned with this application, or claims an invention made as a result of activities undertaken within the scope of a joint research agreement. 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 108-116 and 120-131 are rejected on the ground of nonstatutory obviousness-type double patenting as being unpatentable over claims 1-9 of Fisher; Charles J. Jr. et al. (US 12409260 B2). Regarding pending claim 108, Fisher claims a method capable of treating or inhibiting reactivation of Epstein-Barr Virus (EBV), in a patient, which has experienced a coronavirus infection (claim 1, A method of treating or inhibiting sequelae associated with SARS-COV-2 in a long COVID patient); the method comprising: a) introducing blood or plasma from the patient into the extracorporeal device comprising a lectin (claim 1, (a) introducing blood or plasma from the patient into an extracorporeal device comprising a lectin); wherein the patient does not presently have a coronavirus infection and/or EBV infection but exhibits symptoms or sequela of a coronavirus infection and/or EBV infection (claim 1, wherein the patient is a previously SARS-COV-2 infected patient having a reduced or undetectable viral load and exhibiting SARS-COV-2 sequelae that continue for more than 12 weeks post SARS-COV-2 infection); wherein the blood or plasma from the patient comprises a portion of a coronavirus or a portion of EBV or both (claim 2, wherein the blood or plasma from the patient comprises a spike protein or S1 of SARS-COV-2); b) contacting the blood or plasma from the patient with the lectin in the extracorporeal device for a time sufficient to allow the portion of the coronavirus or the portion of EBV or both in the blood or plasma to bind to said lectin (claim 1, (b) contacting the blood or plasma from the patient with the lectin in the extracorporeal device for a time sufficient to allow the portion of SARS-COV-2 present in the blood or plasma to bind to said lectin); and c) reintroducing the blood or plasma obtained after (b) into said patient, wherein the blood or plasma obtained after (b) has a reduced amount of the portion of the coronavirus or the portion of EBV or both as compared to the blood or plasma of said patient prior to (b) (claim 1, (c) reintroducing the blood or plasma obtained after (b) into said patient, wherein the blood or plasma obtained after (b) has a reduced amount of the portion of SARS-COV-2 as compared to the blood or plasma of said patient prior to (b)); thereby treating or inhibiting reactivation of the coronavirus in the patient (claim 1, thereby treating or inhibiting the sequelae associated with SARS-COV-2 in the patient). Fisher does not explicitly claim that the method treats or inhibits reactivation of EBV in a patient. However, this claim describes coronavirus infection and/or EBV infection in the alternative in each step. Fisher explicitly claims a method that treats or inhibits sequelae of SARS-COV-2. Also, Fisher’s method performs all of the same steps as the claimed method. The only difference appears to be in the expected outcome, which treats or inhibits reactivation of EBV instead of for SARS-COV-2. Fisher’s method performs the same steps of the claimed method and therefore appears suitable for treating sequalae of both EBV and SARS-COV-2. Regarding pending claim 122, Fisher claims a method capable of treating or inhibiting reactivation of Epstein-Barr Virus (EBV), in a patient, which has experienced a coronavirus infection (claim 1, A method of treating or inhibiting sequelae associated with SARS-COV-2 in a long COVID patient); the method comprising: a) introducing blood or plasma from the patient into an extracorporeal device comprising a hollow fiber cartridge (claim 1, (a) introducing blood or plasma from the patient into an extracorporeal device comprising a lectin; claim 7, wherein the extracorporeal device comprises a hollow fiber cartridge); which comprises a lectin adsorbed to a solid support (claim 5, wherein the lectin is immobilized or adsorbed on to a solid support); wherein the blood or plasma from the patient comprises a portion of a COVID-19 virus (claim 2, wherein the blood or plasma from the patient comprises a spike protein or S1 of SARS-COV-2); b) contacting the blood or plasma from the patient with the lectin in the extracorporeal device for a time sufficient to allow the portion of the COVID-19 virus present in the blood or plasma to bind to said lectin (claim 1, (b) contacting the blood or plasma from the patient with the lectin in the extracorporeal device for a time sufficient to allow the portion of SARS-COV-2 present in the blood or plasma to bind to said lectin); and c) reintroducing the blood or plasma obtained after (b) into said patient, wherein the blood or plasma obtained after (b) has a reduced amount of the portion of the COVID- 19 virus as compared to the blood or plasma of said patient prior to (b) (claim 1, (c) reintroducing the blood or plasma obtained after (b) into said patient, wherein the blood or plasma obtained after (b) has a reduced amount of the portion of SARS-COV-2 as compared to the blood or plasma of said patient prior to (b)). Fisher does not explicitly claim that the method treats or inhibits reactivation of EBV in a patient. However, this claim describes coronavirus infection and/or EBV infection in the alternative in each step. Fisher’s method also performs all of the same steps as the claimed method. Regarding the rationale that Fisher’s method will also treat or inhibit reactivation of EBV, see the discussion of claim 108 above. Regarding pending claims 121 and 130, Fisher claims that the patient does not have detectable circulating coronavirus (claim 1, treating or inhibiting sequelae associated with SARS-COV-2 in a long COVID patient … wherein the patient is a previously SARS-COV-2 infected patient having a reduced or undetectable viral load). Regarding pending claims 109-116 and 123-129, Fisher claims all limitations in patented claims 1-9 as shown in table 1. Table 1: Fisher double patenting Pending claim Fisher Pending claim Fisher Pending claim Fisher 109 3 115 7 126 4 110 1 116 8 127 8 111 2 120 9 128 5 112 4 123 6 129 6 113 5 124 2 131 1 114 6 125 3 Conclusion The prior art made of record and not relied upon is considered pertinent to applicant's disclosure. Sohka; Takayuki et al. US 20100069815 A1 Miao; Wenliang et al. US 20150246170 A1 Van Bruggen; Robin et al. US 20180264186 A1 Any inquiry concerning this communication or earlier communications from the examiner should be directed to: Tel 571-272-2590 Fax 571-273-2590 Email Adam.Marcetich@uspto.gov The Examiner can be reached 8am-4pm Mon-Fri. If attempts to reach the examiner by telephone are unsuccessful, the examiner’s supervisor, Rebecca Eisenberg can be reached at 571-270-5879. The fax phone number for the organization where this application is assigned is 571-273-8300. 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. 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. /Adam Marcetich/ Primary Examiner, Art Unit 3781
Read full office action

Prosecution Timeline

Apr 11, 2024
Application Filed
Mar 20, 2026
Non-Final Rejection — §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
92%
With Interview (+19.5%)
3y 1m
Median Time to Grant
Low
PTA Risk
Based on 1336 resolved cases by this examiner. Grant probability derived from career allow rate.

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