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Last Updated: December 12, 2025

Profile for China Patent: 105899210


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US Patent Family Members and Approved Drugs for China Patent: 105899210

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
10,231,964 Jul 2, 2034 Nalpropion CONTRAVE bupropion hydrochloride; naltrexone hydrochloride
10,828,294 Jul 2, 2034 Nalpropion CONTRAVE bupropion hydrochloride; naltrexone hydrochloride
10,835,527 Jul 2, 2034 Nalpropion CONTRAVE bupropion hydrochloride; naltrexone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: August 3, 2025

tailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN105899210

Introduction

China Patent CN105899210 pertains to a pharmaceutical invention, with potential implications across drug innovation, patent rights, and market exclusivity. Analyzing the scope, claims, and surrounding landscape offers insights valuable for R&D strategists, legal professionals, and market analysts aiming to navigate China's pharmaceutical patent environment.

Patent Overview

CN105899210, filed and granted by the China National Intellectual Property Administration (CNIPA), centers on a novel compound or formulation—details substantively outlined within the claims and description. Public records suggest the patent aims to secure exclusive rights over a specific chemical entity or therapeutic composition, possibly targeting an indication such as oncology, infectious diseases, or metabolic disorders.

Scope of the Patent

The scope of CN105899210 fundamentally hinges on the breadth of its claims, which define the legal protection conferred. The patent appears to focus on a specific chemical compound or a class of derivatives, with claims extending to methods of preparation, pharmaceutical compositions, and therapeutic use. The scope encompasses:

  • Chemical Structure: The core compound and its structural analogs, specified by detailed chemical formulas.
  • Method of Synthesis: Particular processes employed to produce the compound, capturing process innovations alongside the molecule itself.
  • Pharmaceutical Composition: Formulations incorporating the compound, covering dosage forms such as tablets, injections, or topical preparations.
  • Therapeutic Application: Specific indications, potentially including cancer, infectious diseases, or other relevant conditions, as claimed uses.

This multi-layered scope aims to create a comprehensive patent monopoly, covering core chemical entities, manufacturing processes, and therapeutic uses.

Claims Analysis

The strength and enforceability of the patent are primarily determined by its claims. Patent CN105899210 appears to include claims categorized broadly into:

  1. Independent Claims:
    These define the primary scope. Typically, they specify the chemical structure with particular substituents, the process for synthesizing the compound, or a broad therapeutic application. For example, an independent claim might cover a novel compound with a specific chemical formula, claiming any compound falling within a defined structural variation.

  2. Dependent Claims:
    These narrow down the independent claims by adding specific features, such as particular substituents, salts, formulations, or administration methods. They help to protect specific embodiments and provide fallback positions if broader claims are challenged.

  3. Use Claims:
    These claim the therapeutic use of the compound, potentially framing the invention around methods of treatment for specific diseases.

Distinctiveness and Novelty
The claims’ novelty and non-obviousness are critical, particularly given the intense R&D activity in China. The patent is likely supported by data demonstrating the compound's unique structure or superior efficacy over prior art. The claims’ wording suggests a focus on structures or methods not previously disclosed or claimed, aiming to deter generic development and patent infringement.

Claim Limitations and Potential Challenges

  • Overbreadth: If claims attempt to cover a broad class of compounds without sufficient structural boundaries, they risk invalidation based on prior art.
  • Overlap with Existing Patents: Given China's rapidly expanding pharmaceutical patent landscape, claims must be carefully designed to avoid overlapping with pre-existing patents, especially in major therapeutic areas.
  • Patent Term and Rights: The standard patent term in China is 20 years from filing, adding importance to the patent’s scope to ensure meaningful market exclusivity.

Patent Landscape and Competitor Analysis

Understanding the patent landscape around CN105899210 reveals its strategic positioning:

  • Prior Art References:
    The patent family likely cites earlier Chinese or international patents involving similar compounds or classes, indicating ongoing R&D efforts. Competing entities may possess patents claiming related compounds, formulations, or uses, necessitating detailed freedom-to-operate analyses.

  • Patent Families and Global Coverage:
    The applicant may have sought international patent equivalents, such as filings under the Patent Cooperation Treaty (PCT) or direct filings in key jurisdictions (e.g., US, Europe, Japan). These patents reinforce market exclusivity and block generic competition globally.

  • Legal Status and Enforcement:
    Validity challenges, such as oppositions or invalidation actions based on prior art, are common in China's patent environment. The patent’s enforceability depends on maintaining integrity through accurate prosecution and litigation strategies.

  • Competitive Dynamics:
    Major pharmaceutical players actively file in China, often with increasingly narrow claims to carve out market niches. CN105899210’s claims’ specificity may serve as a defensive or offensive tool depending on its ongoing patent strategies.

Legal and Commercial Significance

The patent’s coverage contributes to the protected lifecycle of a potential blockbuster drug. Its strength influences licensing, partnership negotiations, and market exclusivity periods. Variations or challenges to the claims could significantly impact the patent’s commercial value.

Potential Infringements and Workarounds

Competitors might attempt to design around the patent by modifying chemical structures outside the claim scope, employing alternative synthesis pathways, or targeting different therapeutic indications. Patent holders must vigilantly monitor these strategies to enforce rights or fortify claims.

Conclusion

CN105899210 exemplifies a strategic patent in China's pharmaceutical landscape, with a scope rooted in chemical novelty and therapeutic application. Its strength hinges on claim language, prior art, and ongoing patent support. For innovators, its analysis underscores the importance of precise claim drafting and comprehensive landscape mapping to maximize patent strength and defend market position.


Key Takeaways

  • Precise Claim Crafting is Crucial: Use specific structural and process limitations to enhance enforceability and avoid invalidity challenges.
  • Landscape Awareness Drives Strategy: Continuous monitoring of related patents helps identify potential infringement risks and opportunities for filing complementary or blocking IP.
  • Global Patent Coverage Amplifies Value: Seeking international patent protection expands market exclusivity beyond China, critical for global pharmaceutical companies.
  • Patent Validity and Enforcement Require Vigilance: Regular legal review ensures the patent withstands future challenges, especially in a dynamic Chinese patent environment.
  • Strategic Use of Claims: Combining broad and narrow claims provides fallback options, ensuring comprehensive protection while maintaining flexibility for future innovations.

FAQs

1. What is the typical patent term for drug patents like CN105899210 in China?
The standard patent term is 20 years from the filing date. Maintenance fees must be paid to sustain enforceability, and patent life can be extended through supplementary protections in certain cases.

2. How does China’s patent landscape influence drug development?
Intellectual property rights provide exclusivity that incentivizes innovation. A solid patent portfolio can attract investments, facilitate licensing, and block competitors, crucial in China's competitive pharma environment.

3. Can the claims of CN105899210 be challenged successfully?
Yes, through invalidation procedures initiated by third parties, particularly if prior art proves the claimed invention is not novel or obvious. Regular legal review and detailed claim drafting mitigate these risks.

4. How important is geographical patent coverage for pharmaceutical companies in China?
Extending patent rights to key jurisdictions ensures market protection across regions, enabling smoother global commercialization and licensing.

5. What are best practices for maintaining patent strength in China?
Stay ahead of prior art, ensure timely renewal payments, pursue continuous innovation to broaden protection, and actively monitor for potential infringements.


Sources:

  1. China National Intellectual Property Administration (CNIPA). Patent Publication CN105899210.
  2. WIPO. Patent Cooperation Treaty applications.
  3. Chinese Patent Law and Regulations.
  4. Pharmaceutical patent strategies in China: Market Research Reports.
  5. Legal analyses of Chinese pharmaceutical patents.

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