Changeflow GovPing Pharma & Drug Safety Aspirin Oral Mucosal Formulations
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Aspirin Oral Mucosal Formulations

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Summary

USPTO published patent application US20260090985A1 for oral mucosal aspirin formulations (91-200mg micronized) with buffer and surfactant components. The application, filed by inventor James Dzandu, covers sublingual and buccal delivery formulations with pH ≤3. No regulatory obligations or compliance deadlines are imposed by this patent publication.

What changed

USPTO published patent application US20260090985A1 on April 2, 2026, disclosing pharmaceutical formulations comprising micronized aspirin (91mg to 200mg), a buffer, a surfactant, and pharmaceutically acceptable excipients for oral mucosal (sublingual and/or buccal) administration. The formulations are characterized by a pH ≤3 when dissolved in 1mL distilled water. The application also discloses methods of treating subjects by administering these formulations. Filing occurred on October 2, 2025, under application number 19348728.

This is a patent application publication, not a regulatory requirement or enforcement action. It creates no compliance obligations or deadlines. Pharmaceutical companies and drug manufacturers developing aspirin delivery systems should review the claims to assess potential freedom-to-operate implications or licensing opportunities. The patent remains pending examination and has not yet been granted.

Archived snapshot

Apr 2, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← USPTO Patent Applications

ORAL MUCOSAL FORMULATIONS OF ASPIRIN

Application US20260090985A1 Kind: A1 Apr 02, 2026

Inventors

James Dzandu

Abstract

Disclosed herein, in part, are pharmaceutical formulations for oral mucosal (e.g., sublingual and/or buccal) administration comprising micronized aspirin, (e.g., 91 mg to 200 mg micronized aspirin), a buffer, a surfactant, and one or more pharmaceutically acceptable excipients, wherein the pH of a solution of the formulation dissolved in 1 mL distilled water is less than or equal to 3. Methods of treating a subject in need thereof comprising administering one or more disclosed pharmaceutical formulations to the subject are also provided herein.

CPC Classifications

A61K 9/006 A61K 9/1611 A61K 9/1617 A61K 9/1629 A61K 31/192 A61P 9/04

Filing Date

2025-10-02

Application No.

19348728

View original document →

Named provisions

Abstract CPC Classifications Filing Date

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Last updated

Classification

Agency
USPTO
Published
April 2nd, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Draft
Change scope
Minor

Who this affects

Applies to
Pharmaceutical companies Drug manufacturers
Industry sector
3254 Pharmaceutical Manufacturing
Geographic scope
United States US

Taxonomy

Primary area
Intellectual Property
Operational domain
Legal
Topics
Pharmaceuticals Healthcare

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