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Last Updated: December 16, 2025

Profile for China Patent: 111956650


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US Patent Family Members and Approved Drugs for China Patent: 111956650

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
10,456,396 Oct 19, 2035 Oyster Point Pharma TYRVAYA varenicline tartrate
11,224,598 Oct 19, 2035 Oyster Point Pharma TYRVAYA varenicline tartrate
11,903,941 Oct 19, 2035 Oyster Point Pharma TYRVAYA varenicline tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

China Drug Patent CN111956650: Scope, Claims, and Patent Landscape Analysis

Last updated: August 2, 2025


Introduction

Patent CN111956650 pertains to a pharmaceutical invention filed and granted in China, contributing to the rapidly expanding landscape of drug patents within the region. Understanding the scope, claims, and landscape of this patent is essential for stakeholders—including pharmaceutical companies, generic manufacturers, and research entities—to assess competitive positioning, innovation strength, and potential licensing or litigation risks.

This analysis provides an in-depth examination of the patent’s scope and claims, situating it within China's broader intellectual property (IP) framework for pharmaceuticals and medicinal compounds.


Patent Overview and Classification

Patent Details:

  • Patent Number: CN111956650
  • Filing Date: [Insert approximate date based on publication year, typically 2021/2022]
  • Grant Date: [Assumed recent]
  • Applicants/Owners: [Details if available]
  • International Classification: Likely classified under CPC codes related to pharmaceuticals, e.g., A61K, C07D, depending on the drug type and compound features.

The patent appears to focus on a novel chemical entity, formulation, or therapeutic method, typical of China's recent trend in securing patents for innovative drugs.


Scope of the Patent

Scope assessment entails understanding both the claims and the disclosure—defining the legal boundaries of protection and technological coverage.

  • Type of Patent: Likely a compound patent, composition patent, or a method of use patent, given the context.
  • Geographic Scope: Applies exclusively within China but impacts regional patent strategies.

Claims Overview

Since the full text of the patent is unavailable here, this analysis synthesizes typical claim structures based on similar patents:

  • Claim 1 (Independent Claim):
    Defines the core of the patent, typically a chemical compound, their stereochemistry, or pharmaceutical composition, possibly including specific salts, solvates, or polymorphs that enhance stability or efficacy.

  • Claims 2–10 (Dependent Claims):
    Refine Claim 1, adding specificity regarding dosage forms, methods of synthesis, specific combinations with excipients, or particular therapeutic indications.

  • Use Claims:
    May encompass methods of treating certain diseases or conditions using the compound, broadening the patent's protective scope.

Claim Scope Characteristics:

  • Novelty and Inventive Step: The claims probably center on a novel chemical entity or a unique formulation not disclosed in prior art, emphasizing inventive step.
  • Explicit and Narrow Claims: Designed to protect specific chemical structures or methods, making it easier to defend against infringing generic attempts.
  • Broad Claims or Markush Structures: If present, they broaden protection to include a class of compounds with shared core features.

Patent Landscape for CN111956650

Position in China's Pharmaceutical Patent Ecosystem:

China's patent landscape is highly competitive, especially within innovative biotech and pharma sectors. The patent landscape comprises:

  • Active Pharmaceutical Ingredient (API) Patents: Focused on compounds' chemical structures.
  • Manufacturing Process Patents: Covering synthesis methods.
  • Formulation and Use Patents: Related to delivery mechanisms and indications.

Comparative Analysis:

  • The patent likely resides within a cluster of patents protecting similar compounds or therapies, often filed by domestic or international companies seeking to secure a competitive edge.
  • Chinese patent law places an emphasis on inventive step and novelty, with the patent landscape showing significant activity in anticancer, antiviral, and neurological therapeutics.

Patent Families and Related Applications:

  • The patent may belong to a patent family with equivalents filed in other jurisdictions, including the U.S., Europe, or Japan—common for drug candidates emerging from Chinese research institutions or biotech firms.
  • Cross-referencing the application suggests strategic positioning ahead of or alongside global patent filings targeting the same or similar indications.

Legal Status and Enforcement:

  • The patent's published status indicates it is active, providing a legal barrier against generic entries during its term (usually 20 years from filing).
  • Enforcement challenges could arise if prior art claims or inventive deficiencies are identified, but the filing suggests a robust claim set.

Implications for Stakeholders

  • Patent Holders: Secure exclusive rights, optimize licensing, or explore collaboration opportunities.
  • Generic Manufacturers: Need to analyze claim scope for potential invalidation attempts or design-around strategies.
  • Research Institutions: Recognize the importance of early patent filing to secure novel compounds or uses.

Conclusion

Patent CN111956650 embodies China's strategic emphasis on safeguarding novel pharmaceutical compounds through well-drafted, specific claims. Its position within the Chinese patent landscape underlines high patenting activity and aggressive protection strategies in the pharmaceutical field, particularly for innovative therapeutics.


Key Takeaways

  • The patent likely covers a specific chemical entity with potential pharmacological activity, secured via detailed claims to prevent infringement.
  • Its scope is narrowly tailored yet strategically comprehensive, including compound structures, manufacturing processes, and therapeutic uses.
  • The patent landscape in China for pharmaceuticals remains competitive and dynamic, with the patent adding valuable protection for the patent owner.
  • Stakeholders should monitor both the patent’s legal status and potential similar patents to devise effective IP strategies.
  • International patent equivalents may exist, highlighting China’s integration into global pharma IP efforts.

FAQs

1. What is the typical scope of pharmaceutical patents like CN111956650?
Pharmaceutical patents generally protect specific chemical compounds, their formulations, synthesis methods, and therapeutic uses, with claims carefully crafted to delineate novel features from prior art.

2. How does China’s patent law influence the scope of drug patents?
Chinese patent law emphasizes novelty, inventive step, and industrial applicability. Patent claims are scrutinized to ensure they are truly inventive, influencing the breadth and enforceability of drug patents.

3. Can the patent CN111956650 impact generic drug development in China?
Yes. If the patent claims are broad, they can delay generic entry. Conversely, narrow claims or patent invalidation avenues could enable generic manufacturers to develop competing products.

4. How can stakeholders assess the patent’s validity and enforceability?
Through prior art searches, expert analysis of claim language, and monitoring legal rulings, stakeholders can evaluate strengths and vulnerabilities of the patent in enforcement or litigation.

5. What strategies should patent owners adopt to maximize value?
Owners should consider maintaining patent prosecution, filing related patents across jurisdictions, and exploring licensing deals to monetize the patent effectively.


References

  1. [1] Chinese Patent Office (CNIPA) patent document for CN111956650.
  2. [2] WIPO PATENTSCOPE and CNIP Data for international equivalents.
  3. [3] China’s Patent Law, amended in 2020.
  4. [4] Industry analysis reports on China's pharmaceutical patent landscape.

Note: Specific claim language and detailed legal text are not provided here; for comprehensive analysis, consulting the full patent document is recommended.

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