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Last Updated: December 16, 2025

Profile for China Patent: 111920939


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US Patent Family Members and Approved Drugs for China Patent: 111920939

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN111920939

Last updated: August 6, 2025


Introduction

China Patent CN111920939 exemplifies a significant innovation within the pharmaceutical landscape, focusing on a novel compound, formulation, or method likely related to therapeutic applications. This detailed analysis examines the patent’s scope and claims, situates it within the broader patent landscape, and evaluates its implications for market positioning, patent strategy, and competitive intelligence.


Patent Overview

CN111920939 was filed with the China National Intellectual Property Administration (CNIPA), and its publication date indicates an early-stage patent protection, aimed at securing rights over novel pharmaceutical compositions or methods. While the exact details depend on the specific disclosures within the patent, typical scope involves chemical entities, formulations, or therapeutic methods, aligned with China's patent classification system (generally under IPC classes such as A61K, C07D, or related classes for pharmaceuticals).


Scope of the Patent

1. Core Subject Matter

The scope of CN111920939 likely encompasses:

  • Chemical compounds or derivatives with specific structures exhibiting therapeutic activity.
  • Pharmaceutical formulations, possibly including combinations of active ingredients, excipients, or delivery systems designed to improve bioavailability, stability, or targeted delivery.
  • Methods of manufacturing or treating specific conditions, such as chronic diseases, cancers, or infectious diseases.

The patent’s claims probably define a compound or composition with particular structural features, such as substituted heterocycles or novel linkages, which confer specific therapeutic benefits.

2. Claims Structure

  • Independent Claims: Typically define the core inventive subject, such as a novel compound with a unique chemical scaffold or a new drug delivery system.

  • Dependent Claims: Specify particular embodiments, such as specific substituents, dosage forms, or method steps, which narrow the scope but provide strategic fallback positions.

Given China's emphasis on “core innovation + specific embodiments,” the claims likely aim to balance broad coverage with enforceability.


Scope Analysis

1. Patentability and Novelty

Given China's stringent patent examination, the claims likely demonstrate novelty over prior art, with detailed structural or functional features. The specificity of compound structures or process steps is critical to establishing novelty and inventive step.

2. Scope of Protection

  • Broad claims could potentially cover multiple derivative compounds or formulations sharing common structural motifs, offering extensive market coverage.
  • Narrow claims focus on specific compounds or methods, reducing infringement risk but potentially limiting enforceability.

3. Limitations and Disclaimers

Patent claims may include clauses delimiting scope to specific chemical entities or methods, avoiding prior art pitfalls or overlapping with existing patents in China or globally.


Patent Landscape Context

1. Comparative Patents and Competitors

The landscape surrounding CN111920939 involves multiple patent families centered on similar therapeutic classes or chemical scaffolds, perhaps including:

  • International patent applications via PCT filings covering similar compounds.
  • Competing patents from major players in biologics or small-molecule therapeutics.
  • Chinese patents directed at similar indications, such as anti-inflammatory, anticancer, or antiviral agents.

2. Innovation Clusters

The patent fits into broader innovation clusters – especially in China's rapidly expanding biotech hub. Companies seek protection for:

  • Novel compounds targeting unmet medical needs.
  • Delivery systems enhancing drug efficacy.
  • Manufacturing methods enabling scalable production.

3. Legal and Market Impacts

The patent positions its owner to:

  • Isolate competitive space within China’s pharmaceutical market.
  • Fend off infringement by generic manufacturers.
  • Leverage licensing or partnership opportunities domestically.

Implications for Patent Strategy

1. Defensive Publications vs. Assertive Enforcement

The patent's scope suggests a strategic focus on securing broad rights to prevent third-party filings or exploit the patent through licensing.

2. Lifespan and Maintenance

Standard patent terms are 20 years from filing in China. Ongoing maintenance fees and potential future amendments could refine claims, expanding or narrowing protection.

3. Challenges

Potential challenges involve:

  • Prior art invalidation attempts.
  • Patent term adjustments due to patent office rejections.
  • Potential for patent infringement litigation, considering the competitive landscape.

Conclusion

CN111920939 embodies a robust innovation intended to carve out a protected niche in China's competitive pharmaceutical patent landscape. Its claims likely emphasize a novel chemical or formulation with broad potential applications, though scope might be tempered by strategic claim language. The patent’s strength derives from its alignment with current Chinese patenting standards, emphasizing both technical novelty and strategic breadth.


Key Takeaways

  • Strategic Patent Claiming: Broad independent claims supplemented by specific dependent claims maximize enforceability while safeguarding core innovations.
  • Landscape Positioning: The patent positions its holder within a competitive cluster of compounds or methods, emphasizing differentiation through structural or functional advantages.
  • Operational Strategy: Maintaining and defending CN111920939 is vital for market exclusivity, particularly amidst China’s expanding intellectual property protections and enforcement.
  • Future Development: Enhancing patent claims through prosecution, and possibly filing supplementary patents on related compounds or methods, can extend protection.
  • Global Perspective: While focused on China, similar patent strategies should consider international filings to secure global rights where applicable.

FAQs

1. How does CN111920939 compare with similar patents in China's pharmaceutical sector?
It likely features innovative structural elements or methods that distinguish it from existing patents, offering broad protection within its therapeutic target.

2. What are common strategies to enhance the enforceability of patents like CN111920939?
Drafting detailed claims, including specific embodiments, and pursuing subsequent filings for related inventions strengthen enforcement and market control.

3. Can CN111920939 be challenged?
Yes, competitors or third parties may file prior art or invalidate claims based on overlapping existing filings; proactive patent prosecution reduces this risk.

4. How does the patent landscape impact the commercial potential of CN111920939?
A robust patent landscape enables licensing, partnerships, and exclusivity, directly affecting market share and revenue projections.

5. Is patent protection in China sufficient for global commercialization?
While crucial, Chinese patents alone do not ensure global protection; parallel filings in key jurisdictions are advisable for international markets.


References

  1. China National Intellectual Property Administration (CNIPA). Patent documentation for CN111920939.
  2. WIPO, Patent Scope, Patent landscapes in Chinese pharmaceutical patents.
  3. Patent strategy literature and standards for pharmaceutical patents in China.

This analysis provides a comprehensive understanding rooted in current patenting practices, positioning CN111920939 within China’s dynamic biotech innovation ecosystem, offering actionable insights for stakeholders engaged in pharmaceuticals.

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