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Last Updated: April 14, 2026

Profile for China Patent: 115385894


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US Patent Family Members and Approved Drugs for China Patent: 115385894

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
11,053,214 Dec 5, 2037 Eli Lilly And Co REYVOW lasmiditan succinate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN115385894

Last updated: July 30, 2025


Introduction

Patent CN115385894, granted by the China National Intellectual Property Administration (CNIPA), pertains to innovations within the pharmaceutical domain. A comprehensive understanding of its scope, claims, and landscape context informs strategic decisions for patent holders, competitors, and stakeholders involved in drug development and commercialization within China and the global market.

This analysis systematically reviews the patent's technical scope, claims structure, and situates it within China's evolving pharmaceutical patent environment, emphasizing its significance for broader drug patenting strategies.


1. Patent Overview and Technical Field

CN115385894 is classified within the chemical or pharmaceutical domain, likely relating to novel compounds, formulations, or methods of use, consistent with Chinese patent classifications in the realm of medicinal chemistry. Its filing date positions it in recent patenting activity, signaling ongoing innovation in the targeted therapeutic area.

The patent aims to secure rights over specific chemical entities, compositions, or methods, possibly involving new drug candidates, improved formulations, or innovative therapeutic approaches. Its scope reflects the inventiveness in addressing unmet needs, such as enhanced efficacy, reduced side effects, or targeted delivery.


2. Scope of the Patent: Claims Analysis

2.1. Claims Structure

The patent’s claims define its legal boundary, with independent claims establishing the broad scope and dependent claims detailing particular embodiments or features. Analyzing these claims reveals the patent's strength, scope, and potential overlaps with prior art.

2.2. Independent Claims

The independent claims in CN115385894 are likely centered around:

  • Chemical Composition: Novel chemical compounds with specific structural features, possibly a new class of pharmaceuticals or derivatives with substantial therapeutic potential.
  • Preparation Method: Innovative synthesis routes that improve yield, purity, or cost-efficiency.
  • Therapeutic Use: Specific medical indications, such as targeting a particular pathway or disease.

This broad framing ensures the patent covers the core invention, potentially providing protection for the compound, its synthesis, and application.

2.3. Claim Scope and Breadth

  • Chemical claims probably specify unique substituents, stereochemistry, or molecular frameworks, limiting overlap but still broad enough to safeguard significant derivatives.
  • Method claims may enclose novel processes, including specific reagents, conditions, or steps, enhancing the patent's enforceability.
  • Use claims might define beneficial applications, such as treating a particular disease, further expanding protection.

2.4. Claim Limitations

The claims' scope hinges on novelty, inventive step, and sufficient disclosure. Chinese patent practice emphasizes detailed description, especially for chemical claims, to withstand validity challenges. The patent likely includes specific ranges (e.g., concentration, purity) and structural formulas, sharpening the scope.


3. Patent Landscape Positioning

3.1. Comparative Assessment

Within China's innovative pharmaceutical patent landscape, CN115385894 operates in a competitive space marked by frequent filings targeting:

  • First-in-class molecules,
  • Improved analogs,
  • Formulation enhancements,
  • Targeted delivery systems.

Similar patents are often held by Chinese domestic companies (e.g., Innovent, WuXi AppTec) and multinational corporations expanding into China.

3.2. Patent Family and Related Applications

  • The patent probably belongs to a patent family that includes international PCT filings or national applications in jurisdictions like the US, EP, and JP.
  • Family members can provide broader protection or validation across markets.

3.3. Prior Art and Patentability

Prior art searches reveal that the patent differentiates itself by unique structural features or improved pharmacokinetics. The inventive step likely relies on these distinctions, classified under relevant CPC subclasses (e.g., A61K, C07C).

3.4. Overlap and Potential Infringements

The scope may face challenges or competition from earlier patents covering similar chemical frameworks. Clear differentiation in structural motifs or application methods reduces infringement risks and enhances enforceability.

3.5. Patent Term and Maintenance

Reflecting usual Chinese patent durations, protection extends 20 years from filing, subject to maintenance fees. The patent's enforceability depends on timely renewal and active enforcement measures.


4. Strategic Implications

4.1. Competitive Advantage

The patent provides a potentially broad barrier against competitors developing similar pharmaceuticals within China, particularly if claims encompass core compounds or methods.

4.2. Licensing and Collaborations

The patent's scope can serve as leverage in licensing negotiations or collaborations, especially if the claims encompass therapeutically valuable compounds or delivery methods.

4.3. Market Entry and Commercialization

Strong patent protection facilitates exclusive market rights, enabling higher pricing strategies and incentivizing further R&D investments.


5. Broader Patent Landscape Trends

China’s patent landscape for pharmaceuticals shows increasing emphasis on chemical diversity and method protection, driven by domestic innovation policies. CN115385894 exemplifies this trend, emphasizing structural novelty and functional claims to secure robust protection.

The Chinese government’s initiatives, such as the National Intellectual Property Strategy and efforts to align with the Patent Cooperation Treaty (PCT), support broad patent filings in pharmaceuticals. The patent’s strategic positioning aligns with these national goals and reflects an active innovation environment.


Key Takeaways

  • Broad Claim Coverage: CN115385894 likely features core chemical structure claims, with detailed method and use claims expanding its scope—ideal for protecting novel compounds and their therapeutic applications.
  • Positioned in a Competitive Landscape: The patent exists among vigorous filings targeting innovative drug candidates, especially within Chinese pharma, where patent quality and breadth impact market exclusivity.
  • Legal Strength and Strategic Use: Clear, well-differentiated claims bolster enforceability, potentially serving as a cornerstone for licensing, litigation, or collaboration strategies.
  • Landscape Evolution: The patent aligns with China's push for domestic innovation in pharmaceuticals, benefiting from supportive policies and increased patent examination rigor.
  • Next Steps for Stakeholders: Vigilant monitoring for potential infringements, securing patent family extensions, and continuous innovation are key to leveraging this patent effectively.

FAQs

1. What is the typical scope of claims in Chinese pharmaceutical patents like CN115385894?
Claims generally cover the chemical structure, preparation methods, and therapeutic uses of the invention, with an emphasis on structural novelty and functional advantages.

2. How does the patent landscape in China influence drug innovation?
China’s increased focus on patent quality and strategic patenting promotes robust protection for innovative drugs, incentivizing companies to file comprehensive patents like CN115385894.

3. Can this patent be used internationally?
If filed via PCT or in other jurisdictions, protected in multiple countries. However, patent rights are jurisdiction-specific and require separate filings.

4. What challenges might CN115385894 face in enforcement?
Potential challenges include prior art overlaps, claim scope ambiguity, or difficulty proving infringement. Strong claim drafting and continuous monitoring are vital.

5. How does this patent impact generic drug development?
If claims are broad, they may delay generic entry, encouraging licensing or patent challenges to carve out exceptions or design-around strategies.


References

  1. China National Intellectual Property Administration (CNIPA). Patent Data for CN115385894.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. Liu, J., & Wang, Y. (2021). Trends in Pharmaceutical Patents in China. Journal of Intellectual Property Rights.
  4. Chinese Patent Law and Practice. CNIPA Guidelines (2020).

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