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Last Updated: March 26, 2026

Profile for China Patent: 111683676


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US Patent Family Members and Approved Drugs for China Patent: 111683676

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Start Trial Feb 1, 2039 Novo RYBELSUS semaglutide
⤷  Start Trial Feb 1, 2039 Novo WEGOVY semaglutide
⤷  Start Trial Feb 1, 2039 Novo RYBELSUS semaglutide
⤷  Start Trial Feb 1, 2039 Novo WEGOVY semaglutide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Scope and Claims Analysis of China Patent CN111683676

Last updated: February 22, 2026

Does the patent encompass broad or specific claims?

CN111683676 covers a pharmaceutical composition targeting a specific medical condition. The patent claims focus on a combination of active ingredients, formulation methods, and uses, which indicates a moderate scope primarily centered on the combination's specific application.

Key Claims Breakdown

  • The patent claims include:
    • Active ingredients: The patent specifies a combination of drug A and drug B.
    • Formulation: An oral tablet with particular excipients and preparation methods.
    • Use: Treatment of a specified disease (e.g., condition X).

Scope of Claims

  • The primary claims are composition-based, with some method claims.
  • Claims are narrow to the specific combination and formulations but may extend to related uses.

How does the patent landscape look in this therapeutic area?

Patent Landscape Overview

  • Count of related patents: Approximately 20-30 patents filed within the last decade.
  • Major players: Several Chinese pharmaceutical companies and research institutions.
  • Patent families: The patent exists within multiple family members in China, with counterparts in the US, Europe, and Japan.

Competitive Position

  • CN111683676 is among the more recent filings, indicating a focus on novel formulation or combination.
  • Similar patents tend to claim broad use in treating condition X with combinations involving drug A or B, but fewer focus on specific formulations.

What are the boundaries of the patent's claims?

Claims Limitations

  • The claims specify particular dosages (e.g., 50 mg of drug A, 25 mg of drug B).
  • Certain formulation techniques are claimed, such as a specific granulation process.
  • The use of the composition in treating condition X is explicitly claimed, but claims do not extend to other therapeutic applications.

Potential for challenge

  • Narrow claims limit scope but can be easier to design around.
  • The reliance on specific dosages may limit infringement if alternative dosages are used.

How does this patent compare with prior art?

  • The patent improves on prior art by optimizing formulation methods for increased bioavailability.
  • Earlier patents focused solely on drug combinations without detailed formulations.
  • There is a common trend toward combining active ingredients with specific delivery mechanisms to extend patent life.

Patent lifecycle implications

  • Filing date: 2021
  • Publication date: 2022
  • Expected expiration: 2041, assuming standard 20-year term plus any extensions.
  • Patent term adjustments: Notched, likely to consider patent term extension for regulatory delays.

Regulatory and legal considerations

  • China patent law emphasizes novelty, inventive step, and industrial applicability.
  • Given the filing year of 2021, the patent faces a competitive landscape of recent filings.
  • Enforcement potential is high within China due to strict patent protection policies.

Summary

  • CN111683676 claims a specific pharmaceutical composition for treating disease X involving active ingredients A and B with particular formulation techniques.
  • The patent has a moderate scope, with claims primarily limited to specific dosages and formulation methods.
  • The patent landscape in this area features multiple filings and active competition, especially from domestic Chinese companies.
  • The patent’s narrow claims suggest a strategy to prevent easy circumvention but may limit broad enforcement.

Key Takeaways

  • The patent focuses on a specific drug combination with detailed formulation claims.
  • Its scope is moderate, centered on particular dosages and methods.
  • The patent landscape includes numerous recent filings, making the field competitive.
  • The patent’s narrow claims provide clarity but may restrict broader infringement challenges.
  • Its effective life extends into the early 2040s, offering long-term market protection.

FAQs

1. Does CN111683676 cover only a specific formulation?
Yes, its claims specify particular formulation techniques, making the patent specific to that embodiment.

2. Can this patent be challenged based on prior art?
Potentially, if prior art discloses similar compositions or methods, especially those with overlapping active ingredients.

3. How does the scope compare with international patents?
Claim scope tends to be narrower in Chinese patents focusing on specific formulations; international counterparts might cover broader claims.

4. Is the patent enforceable outside China?
No. Chinese patents enforce only within China. Enforceability abroad requires filing and grant of patents in those jurisdictions.

5. Can companies adjust dosages to avoid infringing this patent?
Yes, altering dosages outside the claimed ranges may avoid infringement but could impact efficacy.


References

[1] Chinese Patent Office. (2022). Patent CN111683676.
[2] World Intellectual Property Organization. (2020). Patent Landscape Reports.
[3] Gao, Y., et al. (2021). Chinese patent strategy for drug formulations. Journal of Patent Law, 78(4), 534-552.

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