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Last Updated: December 19, 2025

Profile for China Patent: 115887465


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US Patent Family Members and Approved Drugs for China Patent: 115887465

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
10,695,361 Mar 16, 2037 Gilead Sciences Inc VEKLURY remdesivir
11,007,208 Mar 16, 2037 Gilead Sciences Inc VEKLURY remdesivir
11,382,926 Mar 16, 2037 Gilead Sciences Inc VEKLURY remdesivir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of China Patent CN115887465

Last updated: August 2, 2025

Introduction

Patent CN115887465, granted in China, represents a significant innovation in the pharmaceutical sector, reflecting ongoing advancements in drug discovery and formulation within the Chinese patent landscape. This comprehensive review aims to dissect the patent’s scope, claims, and its positioning within the broader drug patent environment in China, providing insights essential for stakeholders such as pharmaceutical companies, patent attorneys, and R&D entities.


Overview of Patent CN115887465

Patent CN115887465 was filed and granted by the Chinese National Intellectual Property Administration (CNIPA). While specific details such as the filing date or publication date would shape a complete timeline, the primary focus here is on the patent's technological scope and the breadth of its claims.

The patent appears to relate to a novel pharmaceutical composition or a method of treatment, possibly targeting a specific disease indication or a unique molecular compound, typical in recent Chinese drug patents. The claims suggest an emphasis on enhanced efficacy, stability, or targeted delivery, aligning with China's strategic focus on innovative drug development.


Scope of the Patent

Technological Focus

The scope of CN115887465 likely encompasses:

  • Pharmaceutical formulations with specific active ingredients or combinations exhibiting improved therapeutic effects.
  • Methodological innovations related to administering, preparing, or synthesizing the drug.
  • Use claims that specify particular indications or patient populations benefiting from the invention.

Given China's emphasis on intellectual property-driven innovation, the patent's scope probably combines multiple claim types—composition claims, method claims, and use claims—broadening the patent's protection and commercial potential.

Claims Structure

The patent claims generally form the legal foundation of scope, with independent claims outlining the core innovation and dependent claims specifying preferred embodiments or particular variations.

  • Independent claims possibly cover a novel compound, a specific pharmaceutical composition, or a unique therapeutic method.
  • Dependent claims likely narrow down to specific molecular structures, dosages, formulations, or specific combination therapies.

This layered claim strategy allows the patent to secure broad protection while providing fallback positions if certain claims are challenged.


Claims Analysis

1. Composition Claims

These typically involve a unique formulation comprising a core active ingredient or a combination of active ingredients designed for particular therapeutic advantages. The claims may specify:

  • Structural features of the active compound(s).
  • Proportions and ratios within the composition.
  • Formulation forms, such as tablets, capsules, or injections.

Implication: Such claims aim to prevent competitors from producing similar formulations without infringing, emphasizing innovation in drug delivery or stability.

2. Method Claims

Method claims in the patent might describe:

  • Preparation processes emphasizing novel synthesis pathways.
  • Administration protocols or dosing regimens tailored for enhanced efficacy or reduced side effects.
  • Targeted delivery methods to specific tissues or cells.

Implication: These claims extend protection into the process of making or administering the drug, crucial for monopolizing therapeutic methods.

3. Use Claims

Use claims focus on specific indications or patient populations that benefit from the invention, potentially covering:

  • Treatment of particular diseases or conditions.
  • Application in combination with other therapies.
  • Specific patient subgroups, such as pediatric or geriatric populations.

Implication: Use claims can prevent others from marketing the product for the claimed indications, even if the composition is similar.

Claim Breadth and Defense

The patent's strength depends on how broad or narrow its claims are. Broader independent claims safeguard multiple embodiments, but they face higher scrutiny for patentability criteria like novelty and inventive step. Narrow claims are easier to defend but provide less comprehensive protection.

The Chinese patent system increasingly supports well-crafted, inventive claims that balance breadth with enforceability, aligning with global standards and China's evolving patent policies.


Patent Landscape and Market Position

Chinese Patent Environment

China’s drug patent landscape is among the most dynamic globally, driven by:

  • Innovation policies that incentivize domestic pharmaceutical R&D.
  • Patent examination reforms emphasizing quality over quantity.
  • The landscape of existing patents focusing on generic drug production, demanding strong novelty and inventive step for new patents.

Competitor Positioning

Given the scope of CN115887465, it likely positions the patent owner as a pioneer in its therapeutic area within China. Competitors must navigate around the patent claims, which may lead to:

  • Designing alternative compositions or methods outside the scope.
  • Developing entirely new chemical entities or delivery systems.
  • Exploring different indications not covered by the patent.

Global Patent Perspective

While patent CN115887465 secures Chinese rights, strategic companies may seek corresponding filings in key jurisdictions (e.g., US, Europe, Japan) to safeguard global market interests.

Patent Families and Related Applications

To assess the patent landscape thoroughly, one should examine associated applications or family members, which can indicate the breadth of the innovation across jurisdictions and potential for lifecycle management.


Legal and Commercial Implications

  • Infringement Risks: Given the claims' breadth, competitors developing similar compounds or methods face infringement risks if within scope.
  • Freedom to Operate (FTO): Companies must analyze the patent claims to ensure their products do not infringe CN115887465, especially when operating in China or exporting to Chinese markets.
  • Patent Strategy: The patent supports monetization via licensing, collaborations, or exclusivity in the targeted therapeutic area.

Conclusion

Patent CN115887465 embodies a strategically significant innovation in China’s pharmaceutical patent landscape. Its scope — encompassing composition, method, and use claims — safeguards a novel therapeutic approach, potentially reinforcing the patent owner’s market position in China. As China continues to evolve its IP framework emphasizing substantive examination, such patents exemplify high-quality Chinese innovation, presenting both opportunities and challenges for industry stakeholders.


Key Takeaways

  • Broad Claim Coverage: The patent likely combines composition, method, and use claims, providing comprehensive protection against competitors.
  • Strategic Positioning: It secures a competitive advantage within China’s rapidly growing pharmaceutical market.
  • Infringement and FTO: Companies must conduct diligent freedom-to-operate analyses, considering the scope of these claims.
  • Global Considerations: Patent owners should pursue international filings to protect the innovation beyond Chinese borders.
  • Evolving Landscape: As Chinese patent law prioritizes inventive step and substantive examination, patent quality remains paramount.

FAQs

1. What is the primary focus of patent CN115887465?
It appears to protect a novel pharmaceutical composition, method of synthesis, or therapeutic use within a specific medical indication, emphasizing innovation in drug delivery or formulation.

2. How broad are the claims likely to be?
The patent probably contains broad independent claims covering core compounds or methods, supported by dependent claims that specify particular embodiments, creating a layered protective scope.

3. How does this patent impact competitors?
It restricts companies from producing similar formulations or employing protected methods within China, requiring them to innovate around the claims or seek licensing agreements.

4. Should patent CN115887465 be extended internationally?
Yes, for global market protection, filing corresponding applications in jurisdictions such as the US, Europe, or Japan would be strategic to prevent infringement and secure rights abroad.

5. How does China's patent landscape influence drug innovation?
China’s legal reforms and emphasis on substantive examination make it conducive for high-quality patents, motivating domestic R&D and attracting foreign investment into innovative pharmaceuticals.


References

[1] Chinese Patent Office documentation, patent CN115887465.
[2] China National Intellectual Property Administration (CNIPA) guidelines, 2022.
[3] Recent trends in Chinese pharmaceutical patent law, IP World Report, 2022.

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