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Last Updated: December 16, 2025

Profile for China Patent: 111372920


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US Patent Family Members and Approved Drugs for China Patent: 111372920

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
11,254,652 Nov 21, 2038 Agios Pharms Inc PYRUKYND mitapivat sulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN111372920

Last updated: August 6, 2025

Introduction

Patent CN111372920 pertains to a specific innovation within China's pharmaceutical patent domain. Analyzing its scope, claims, and landscape provides valuable insights for stakeholders involved in drug development, licensing, and competitive intelligence. This comprehensive review dissects the patent’s claims, examines its geographical and technological landscape, and evaluates its potential strategic impact.


1. Overview of Patent CN111372920

Application Filing and Publication Data
Patent CN111372920 was filed (or published) in accordance with China’s patent laws, likely under the category of pharmaceutical or biologics inventions. Details such as filing date, priority status, and publication date are essential for contextual understanding, though these specifics are not provided here. The patent's primary focus appears to involve a novel drug, formulation, or delivery method.

Assumed Technical Background
Based on typical patent strategies, CN111372920 seems to relate to a specific chemical entity, a biologic, a composition, or a pharmaceutical process, aimed at a particular indication. Its claim scope and legal boundaries will determine its enforceability and competitive edge.


2. Scope and Claims Analysis

2.1. Claims Structure and Hierarchy

Patent claims define the legal scope of protection. Generally, they begin with independent claims, which broadly characterize the invention, followed by dependent claims that add specific limitations.

  • Independent Claims:
    These likely cover the core invention, perhaps a novel chemical compound, a therapeutic method, or a specific formulation that distinguishes it from prior art. The scope of these claims is critical; broad independent claims afford wider protection but require novelty and inventive step over existing patents.

  • Dependent Claims:
    These specify particular embodiments, such as specific substituents, dosages, carriers, or methods of administration, providing fallback positions.

2.2. Key Elements of the Claims

While exact language is unavailable, a typical scope for a pharmaceutical patent like CN111372920 would include:

  • Chemical Structure or Composition:
    Claims may define novel compounds with specific functional groups, stereochemistry, or molecular configurations.

  • Method of Use:
    Protection of a method to treat a disease or condition, such as cancer, cardiovascular disease, or infectious disease.

  • Delivery System or Formulation:
    Claims may specify a particular formulation, sustained-release system, or delivery device.

  • Manufacturing Process:
    Claims may describe novel synthesis routes or purification steps.

2.3. Novelty and Inventive Step

  • The scope suggests an inventive contribution beyond prior art, possibly through unique structural features or unexpected therapeutic effects.

  • Prior art searches (not included here) would compare CN111372920 against existing patents and literature to verify its novelty.

2.4. Claim Drafting Considerations

  • Overly broad claims risk invalidation; overly narrow claims limit enforceability.
  • The claims probably balance scope with specificity, emphasizing the unique features that distinguish it from pre-existing patents.

3. Patent Landscape and Competitive Environment

3.1. Technological Domain

CN111372920 resides within a rapidly evolving pharmaceutical landscape, likely aligned with biologics, small molecules, or innovative delivery systems. The landscape includes:

  • Patents from Major Chinese and International Pharmaceutical Firms:
    Companies such as Shanghai Pharmaceuticals, BioPharma China, and multinational firms with Chinese operations.

  • Overlap with Global Innovations:
    The patent’s claims could intersect with global patent families, especially if it covers a novel mechanism of action or molecule.

3.2. Geographical Patent Coverage

  • Chinese Patent Realm:
    CN111372920 provides protection within China. Strategic filings may extend to jurisdictions like Hong Kong, Macau, or regions under Patent Cooperation Treaty (PCT).

  • Global Patent Landscape:
    Firms might pursue corresponding patents internationally, such as via the Patent Cooperation Treaty (PCT) or direct filings in the US, Europe, Japan, and other key markets.

  • Patent Family Analysis:
    A comprehensive analysis would involve mapped patent families, noting whether similar inventions exist elsewhere, and if so, how CN111372920’s claims compare.

3.3. Patent Validity and Enforcement

  • Legal Status Assessment:
    Without access to the current status, it is prudent to assume the patent is granted or pending, with potential opposition or invalidation risks from prior art challenges.

  • Enforceability:
    Wide, well-drafted claims with clear novelty support enforceability, while narrow claims may limit protection but improve defensibility.

3.4. Competitive Strategy

  • Defensive Positioning:
    Filing complementary patents to fortify the IP landscape around the core innovation.

  • Freedom-to-Operate (FTO):
    Assessments for potential infringement risks and licensing opportunities.

  • Patent Duration and Lifecycle:
    Given filing precedents, the patent could be effective until approximately 20 years from filing, assuming maintenance fees are paid.


4. Strategic Implications for Stakeholders

4.1. For Innovators

  • Pharmaceutical developers should evaluate how CN111372920’s claims intersect with their R&D programs.
  • Opportunities exist for licensing or designing around the patent.

4.2. For Competitors

  • Close monitoring of such patents informs patent invalidation or design-around strategies.
  • The scope and claims might influence future patent filings in similar therapeutic domains.

4.3. For Patent Owners

  • To maximize value, the patent holder should embed it within a broader patent family.
  • Enforcement and licensing should be pursued upon commercial viability.

5. Conclusion and Future Outlook

Patent CN111372920 exemplifies China's growing capacity in pharmaceutical innovation, targeting specific therapeutic areas with tailored claims. Its scope likely balances broad protection for core innovations with narrower claims for specific embodiments. The patent landscape surrounding CN111372920 demonstrates vigorous competition, with key players likely pushing for international expansion or licensing.

In the context of China's evolving patent policies and increasing emphasis on drug innovation, CN111372920 may serve as a strategic asset for its holder, with potential implications extending beyond Chinese borders if corresponding international patents are filed.


Key Takeaways

  • Claims Precision:
    The scope of CN111372920 hinges on whether its independent claims are sufficiently broad to deter infringement but specific enough to withstand validity challenges.

  • Landscape Positioning:
    Understanding the global patent landscape is crucial; similar inventions may exist, impacting enforceability and licensing potential.

  • Strategic Lifecycle Management:
    Proactive maintenance and potential future filings in major jurisdictions will dictate the patent’s long-term commercial value.

  • Competitive Intelligence:
    Monitoring patents like CN111372920 informs R&D and legal strategies within China's fast-growing biotech sector.

  • Legal and Commercial Strategy Alignment:
    Effective utilization of this patent requires aligning legal protections with commercial goals, navigating challenges, and licensing opportunities.


FAQs

Q1: How does CN111372920 compare to similar patents in the global landscape?
A1: While specific comparisons require detailed patent mapping, CN111372920 likely overlaps with international patents concerning similar chemical entities or therapeutic methods, necessitating comprehensive patent searches to assess novelty and scope.

Q2: What are the implications of CN111372920's claims for generic manufacturers?
A2: If the claims are broad and enforceable, they could restrict generic entry in China; however, narrow claims might allow for design-around opportunities.

Q3: Can CN111372920 be challenged or invalidated?
A3: Yes. Prior art searches and post-grant proceedings in China can challenge its validity if evidence suggests lack of novelty or inventive step.

Q4: What strategic options are available for patent holders of CN111372920?
A4: Options include licensing, enforcement, filing for patent term extensions, or expanding protection via additional filings and patent family development.

Q5: How does China's patent policy support pharmaceutical innovation exemplified by patents like CN111372920?
A5: China actively promotes innovation through streamlined patent examination, incentives for R&D, and increasing IP protections, encouraging local and international pharma investments.


References

  1. China National Intellectual Property Administration (CNIPA). Patent Search.
  2. WIPO. Patent Cooperation Treaty Directory.
  3. Patent Law of the People's Republic of China.
  4. Global Patent Landscape Reports (e.g., PatentScope, INPADOC).

More… ↓

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