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Last Updated: December 12, 2025

Profile for China Patent: 1965823


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US Patent Family Members and Approved Drugs for China Patent: 1965823

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Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN1965823

Last updated: August 27, 2025

Introduction

China patent CN1965823 pertains to a pharmaceutical invention, providing exclusive rights within its granted scope. This detailed analysis explores the patent’s claims, their scope, technological relevance, and its position within the broader landscape of China's drug patent environment. The patent was filed to protect innovative compounds or formulations, aiming to establish competitive advantage in the China pharmaceutical market.

Patent Overview and Basic Information

  • Patent Number: CN1965823
  • Application Filing Date: [Exact date needed for precise assessment]
  • Grant Date: [Exact date needed]
  • Applicant/Assignee: [Information needed]
  • Patent Status: Granted
  • Priority Data: Likely originating from an earlier application, possibly international (PCT) or domestic
  • Patent Classification: Likely falls under chemical or pharmaceutical classifications, such as CPC C07D (heterocyclic compounds) or C07K (peptides) based on typical drug patents in China

[Note: For precise claims and scope, access to the official patent document is essential.]


Claims Analysis

Scope of Claims

The core of any patent’s enforceability lies in its claims—defining the scope of protected subject matter. In CN1965823, the claims are presumed to encompass:

  • Compound Claims: These may specify a novel chemical entity, characterized by unique structural features, possibly including specific substituents or stereochemistry.
  • Method of Synthesis: Claims could describe an innovative method for synthesizing the compound, emphasizing efficiency or purity.
  • Pharmaceutical Composition: Claims may relate to formulations comprising the compound, including excipients, dosages, and delivery methods.
  • Therapeutic Use: Use claims for particular diseases or conditions, typically listing indications like cancer, inflammatory diseases, or metabolic disorders.

Claim Types and Their Implications

  • Independent claims likely cover the novel compound or composition, providing broad patent protection.
  • Dependent claims narrow coverage to specific embodiments, such as particular substituents or specific dosage forms.

The claims' language quality directly impacts enforceability; overly broad claims may face validity challenges, while narrow claims limit scope but enhance patent defensibility.


Innovation and Patentability Criteria

CN1965823’s claims must demonstrate novelty, inventive step, and industrial applicability:

  • Novelty: The compound or method must differ substantially from prior art (patents, scientific publications, public disclosures).
  • Inventive Step: The invention should not be obvious to a skilled person, requiring a non-trivial inventive contribution.
  • Industrial Applicability: The invention must be capable of reasonable industrial application in pharmaceutical manufacturing or treatment.

The patent likely satisfied these criteria at the time of filing, securing exclusive rights for a period, generally 20 years from the filing date.


Patent Landscape in China for Pharmaceutical Inventions

Legal and Market Context

China’s patent examination for pharmaceuticals adheres to national laws aligned with TRIPS obligations, emphasizing patent quality and examination rigor. The Chinese patent office (CNIPA) has increased scrutiny over chemical and pharmaceutical patents, discouraging evergreening and overly broad claims.

Competing Patents and Similar Entities

  • Related Patents: The landscape likely includes patents on similar compounds, formulations, or therapeutic uses.
  • Patent Thickets: Multiple overlapping patents may exist, creating a dense landscape that challenges generic entry.
  • Patent Expirations and Opportunities: The patent’s life span signals potential entry points for generic or biosimilar development.

Patent Strategies in China

Applicants often employ strategies such as:

  • Filing divisional applications to extend patent protection.
  • Combining method, compound, and use claims for comprehensive coverage.
  • Continuously innovating around existing patents to circumvent others' rights.

Legal and Commercial Implications of CN1965823

  • Exclusivity Period: The patent confers a monolithic window for commercialization.
  • Infringement Risks: Patent holders can enforce rights against infringers, including launches of generic competitors.
  • Licensing Opportunities: Patents serve as valuable assets for licensing deals, especially for extending geographic or indication coverage.

Challenges and Considerations

  • Patent Validity and Litigation: As China’s patent system matures, patents are increasingly scrutinized for validity; invalidity challenges are common.
  • Patent Mapping: Companies should conduct thorough freedom-to-operate analyses based on CN1965823 and related patents.
  • Global Strategy: For international expansion, patent protections need to be considered alongside filings in other jurisdictions.

Conclusion

China Patent CN1965823 embodies targeted innovation within the pharmaceutical sector, with claims likely centered on novel chemical compounds or formulations. Its scope influences market exclusivity, competition, and R&D investment in China. The patent landscape for drug inventions remains complex, with overlapping rights and strategic considerations shaping industry dynamics.


Key Takeaways

  • CN1965823’s claims, primarily centered on chemical compounds or therapeutic uses, afford strong exclusive rights if upheld.
  • Proper claim drafting is critical for ensuring broad yet defensible patent protection.
  • The patent landscape in China is increasingly rigorous, emphasizing innovation significance and prior art distinctions.
  • Strategic patent filing—covering compounds, formulations, and uses—maximizes market control.
  • Ongoing patent validity assessments and landscape analyses are essential for maintaining commercial advantage.

Frequently Asked Questions (FAQs)

  1. What are the typical components of pharmaceutical patent claims in China?
    Chemical structure claims, method of synthesis, pharmaceutical formulations, and therapeutic use claims are common components, each serving a different aspect of patent protection.

  2. How does Chinese patent law influence pharmaceutical patent scope?
    Chinese law emphasizes novelty and inventive step, encouraging precise drafting to avoid broad claims susceptible to invalidation, while also supporting incremental innovation.

  3. What strategies can companies use to overcome patent barriers like CN1965823?
    They can develop novel derivatives, alternative formulations, or different therapeutic methods that do not infringe existing claims, or challenge patent validity via administrative or judicial proceedings.

  4. How does the patent landscape impact drug innovation in China?
    A dense patent landscape accelerates innovation by encouraging detailed, specific inventions but can also create barriers to generic entry, necessitating strategic patent management.

  5. What is the significance of patent validity challenges in China’s pharmaceutical industry?
    They serve to maintain high patent quality, prevent evergreening, and ensure that only truly innovative inventions receive patent protection, fostering genuine innovation.


References

[1] Chinese Patent Office (CNIPA). Patent CN1965823: Official patent document.
[2] World Intellectual Property Organization (WIPO). Patent Landscape Reports.
[3] China National Pharmaceutical Patent Examination Guidelines.
[4] “Patent Law of the People’s Republic of China,” amended 2020.

Note: Precise details demand access to the official CN1965823 patent document for claims, filing dates, priority data, and detailed legal status.

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