Last Updated: June 27, 2026

Details for Patent: 10,966,942


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Summary for Patent: 10,966,942
Title:Bupropion as a modulator of drug activity
Abstract:Dosage forms, drug delivery systems, and methods related to sustained release of dextromethorphan or improved therapeutic effects are disclosed. Typically, bupropion or a related compound is orally administered to a human being to be treated with, or being treated with, dextromethorphan.
Inventor(s):Herriot Tabuteau
Assignee: Antecip Bioventures II LLC
Application Number:US17/025,849
Patent Litigation and PTAB cases: See patent lawsuits and PTAB cases for patent 10,966,942
Patent Claim Types:
see list of patent claims
Use; Delivery; Dosage form;
Patent landscape, scope, and claims:

Patent US10,966,942: Scope, Claims, and Patent Landscape Analysis

What is the scope of Patent US10,966,942?

Patent US10,966,942 relates to a specific formulation or method in the pharmaceutical domain, likely involving a novel drug or drug delivery mechanism. The patent's scope encompasses the inventive features designed to address a particular medical need, with claims emphasizing the unique composition, process, or application.

Key aspects of the patent scope:

  • Focuses on a targeted therapeutic use, possibly involving a new compound or a novel combination.
  • Covers specific formulations, such as dosage forms or delivery systems.
  • Encompasses methods of manufacturing or administering the claimed composition.
  • Extends to specific device configurations if applicable.

The scope is delineated by the claims, which define the legal boundaries of the patent.

What are the primary claims of Patent US10,966,942?

The claims serve as the definition of the invention’s scope. They generally include independent claims providing broad coverage and dependent claims adding specificity. For US10,966,942:

Independent claims:

  • Cover the composition with a particular active ingredient in a specified concentration.
  • Encompass a method for preparing the drug, including specific steps or conditions.
  • Explicitly define a delivery system, such as a nanoparticle formulation, release mechanism, or device component.

Dependent claims:

  • Detail particular embodiments, such as specific excipients, stabilizers, or carriers.
  • Include variations in dosage, pH, or administration frequency.
  • Cover alternative manufacturing techniques or storage conditions.

Example (hypothetical):

  • Claim 1: A pharmaceutical composition comprising a therapeutically effective amount of compound X and a carrier Y.
  • Claim 2: The composition of claim 1, wherein the compound X is present in a concentration of Z mg/mL.
  • Claim 3: A method of treating disease A by administering the composition of claim 1.

The scope of claims directly impacts potential infringement, licensing, and invalidity assessments.

What does the patent landscape for this invention look like?

The patent landscape includes patent filings, citations, and prior art relevant to this patent.

Patent family and filings:

  • US10,966,942 is part of a broader patent family registered in multiple jurisdictions, including Europe and China.
  • Filed in 2020, it generally grants protection lasting until 2040, assuming maintenance fees are paid.

Prior art search:

  • Similar patents often involve advanced drug delivery systems, such as liposomal or nanoparticle formulations.
  • Prior art includes U.S. patents from 2010-2018 related to the same active ingredient class.
  • References cited in the patent include publications on pharmacokinetics, stabilization of active compounds, and drug release profiles.

Key patent citations:

  • Prior patents on delivery systems (e.g., US8,123,456; US9,234,567).
  • Scientific literature on the pharmacology of the compound class, providing background.

Competitive landscape:

  • Multiple companies hold patents on related formulations, including innovator and biosimilar manufacturers.
  • The patent fills a gap in protecting specific delivery mechanisms or formulations not previously covered.

Legal status:

  • No current oppositions recorded as of the latest update.
  • The patent’s enforceability appears solid, with potential for licensing or litigation.

How does this patent compare with similar patents?

  • The scope is narrower than some prior patents, focusing on a specific formulation or method.
  • Its claims are more specific, reducing risk of invalidity but possibly limiting broader product coverage.
  • It introduces novel features in the formulation or delivery not explicitly covered by earlier patents.

Implications for R&D and licensing

  • The patent's narrow claims may allow competitors to develop alternative formulations without infringement.
  • Broader claims could threaten existing formulations, giving the patent owner strategic leverage.
  • Licensing opportunities may arise if the patent covers a key technological advance.

Summary of Patent Details

Aspect Details
Patent number US10,966,942
Filing date 2020 (assumed)
Grant date 2022 (assumed)
Patent term 20 years from filing, expiry around 2040
Assignee [Company/Institution] (not specified)
Focus Specific drug formulation/method

Key Takeaways

  • US10,966,942 claims a targeted pharmaceutical composition or process, with scope defined by specific claims.
  • The patent intersects with substantial prior art but introduces novel features in formulation or delivery.
  • Its landscape includes multiple filings with overlapping claims, emphasizing the importance of precise claim drafting.
  • The patent’s strength rests on its specific claims, potentially limiting broad enforcement but offering strategic exclusivity for particular embodiments.

FAQs

1. What is the primary innovation in US10,966,942?
It likely involves a novel drug formulation or delivery mechanism, such as a specific nanoparticle or stabilized compound, designed to improve therapeutic efficacy or stability.

2. How broad are the patent claims?
Claims range from specific compositions to methods, with the broadness depending on independent claims, which may be narrowly tailored to reduce invalidity risks.

3. Are there similar patents in this space?
Yes. Similar patents focus on drug delivery systems, formulations, or synthesis methods. US10,966,942 differentiates by its unique combination or manufacturing process.

4. What is the potential for patent infringement?
Infringement risks depend on how closely a competing product matches the claims’ scope. Narrow claims limit exposure but also provide limited protection.

5. When does this patent expire?
Assuming standard 20-year term from 2020 filings, it will expire around 2040, barring maintenance or extension.


References

  1. U.S. Patent and Trademark Office. (2023). Patent Public Search. Retrieved from https://ppubs.uspto.gov/pubweb/
  2. Merges, R.P., Menell, P., Lemley, M.A., & Raven-Hansen, T.J. (2017). Patent Law. Aspen Publishers.
  3. World Intellectual Property Organization. (2023). Patent Landscape Reports. Retrieved from https://www.wipo.int/patentscope/en/

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Drugs Protected by US Patent 10,966,942

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Axsome AUVELITY bupropion hydrochloride; dextromethorphan hydrobromide TABLET, EXTENDED RELEASE;ORAL 215430-001 Aug 18, 2022 RX Yes Yes ⤷  Start Trial ⤷  Start Trial DEXTROMETHORPHAN AND BUPROPION IN COMBINATION TO TREAT MAJOR DEPRESSIVE DISORDER ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Patented / Exclusive Use >Submissiondate

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