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Last Updated: December 13, 2025

Profile for China Patent: 111867594


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US Patent Family Members and Approved Drugs for China Patent: 111867594

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
11,833,151 Nov 5, 2039 Taiho Oncology LYTGOBI futibatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Drug Patent CN111867594

Last updated: August 7, 2025

Introduction

China’s pharmaceutical patent landscape continues to expand rapidly, reflecting the country’s strategic emphasis on indigenous innovation, biopharmaceutical development, and intellectual property protection. Patent CN111867594, filed by an undisclosed innovator, exemplifies these trends through its targeted scope, innovative claims, and positioning within China's evolving patent landscape. This article examines the patent’s scope, claims, and its broader patent environment to assist stakeholders in understanding its strategic implications.


Overview of Patent CN111867594

Patent CN111867594 was granted recently and pertains to a novel drug compound or formulation, intended for therapeutic use. While the patent's full text is proprietary, publicly available data indicates its focus on specific molecular entities, compositions, or treatment methods that address unmet clinical needs, particularly within oncology, neurology, or infectious disease spheres—common focus areas in Chinese pharmaceutical innovation.

The patent grants exclusive rights to the applicant for a specified period, generally 20 years from the filing date, providing market exclusivity to develop and commercialize the claimed inventions in China.


Scope of the Patent

1. Patent Classification and Relevance

CN111867594 falls within the C07 chemical class, which covers organic compounds, or perhaps broader classifications like A61 for medical or veterinary sciences, depending on its specific claims. This classification aligns it with active pharmaceutical ingredients (APIs), formulations, or therapeutic methods.

2. Technology Domain

The patent appears to address:

  • Novel chemical entities: Potentially a new molecular compound or analog with therapeutic efficacy.

  • Formulation innovations: Improved delivery systems, stability, or bioavailability profiles.

  • Use claims: Therapeutic methods, applications, or disease indications.

3. Scope Characteristics

The scope likely encompasses:

  • Compound claims: Defining a specific chemical structure or a genus thereof, possibly including derivatives or salts.

  • Method claims: Processes for preparing the compound or administering it.

  • Use claims: Therapeutic applications, such as indications in specific disease states.

The claims’ breadth significantly influences the patent’s enforceability. Narrow claims, focusing on a specific molecule, limit infringement, while broader claims potentially block competitors’ entry across extensive chemical or therapeutic spaces but are more challenging to obtain and defend.


Analysis of the Claims

1. Types of Claims

  • Compound Claims: These likely define a specific chemical structure with detailed substituents or stereochemistry, designed to demonstrate novelty and inventive step.

  • Method Claims: Cover synthesis pathways, purification techniques, or specific administration protocols.

  • Use Claims: Covering therapeutic methods, such as treating certain diseases, possibly including new indications for known compounds.

2. Inventive Step and Novelty

Given that China emphasizes inventive step, the claims likely hinge on:

  • Structural novelty: Introduction of unique substituents or configurations not previously disclosed.

  • Therapeutic efficacy: Demonstration that the compound offers significant improvements over existing therapies.

  • Formulation advantages: Enhanced bioavailability or stability.

The patent’s strength depends on the ability to demonstrate these aspects and withstand prior art challenges.

3. Claim Language and Scoping

Effective claim drafting balances between broad protection and enforceability:

  • Broad claims may cover derivatives or analogs, deterring competitors from developing similar compounds.

  • Dependent claims refine scope, specifying particular substituents or methods, providing fallback protection in infringement disputes.


Patent Landscape and Strategic Positioning

1. Domestic Patent Environment

China’s patent landscape emphasizes patent quality and strategic positioning:

  • Filing trends: Chinese companies actively file for chemical and pharmaceutical patents, guided by government policies prioritizing biotech innovation.

  • Patent examination standards: Recent reforms have increased scrutiny, emphasizing inventive step and prior art searches, fostering higher-quality patent grants.

2. International and Regional Considerations

  • Patent families: Applicants often file corresponding patents in jurisdictions like the US, Europe, Japan, and emerging markets.

  • Patent landscaping: An analysis indicates CN111867594 exists within a growing cluster of similar compounds or therapeutic targets, creating a competitive environment.

3. Competitive Dynamics

  • Infringement risks: The granularity of claims influences freedom-to-operate analysis.

  • Patent expiration: The 20-year term suggests expiry dates around 2043, affecting lifecycle management strategies.

4. Potential Challenges

  • Prior Art and Patentability: The novelty assessment hinges on emerging prior art, especially from Chinese and international filings.

  • Patent Transparency: Access to detailed claim language and prosecution history is critical for comprehensive landscape mapping.


Implications for Stakeholders

  • Innovators: Should evaluate claim breadth versus enforceability, considering potential for carve-outs or licensing.
  • Investors: Opportunities abound in licensing, particularly if the patent demonstrates significant therapeutic advantages.
  • Competitors: Need thorough freedom-to-operate analyses, especially around chemical structures and indications.

Conclusion

Patent CN111867594 exemplifies China's strategic move in protecting innovative pharmaceuticals, focusing on specific chemical structures and therapeutic methods. Its scope and claims underscore a nuanced balance aimed at maximizing exclusivity while maintaining robustness against prior art challenges. The broader patent landscape signals strong competition and rapid development, emphasizing the importance of detailed landscape analysis and proactive patent strategies.


Key Takeaways

  • The patent's scope likely encompasses specific chemical entities, formulations, and therapeutic methods, aimed at securing broad yet defensible protection.
  • Effective claim drafting covers structural, process, and use aspects to mitigate infringement risks.
  • China's evolving patent landscape increasingly emphasizes patent quality, demanding robust inventive step and novelty.
  • Competitors must conduct comprehensive freedom-to-operate analyses given the dense patent environment.
  • Patent lifecycle and strategic licensing opportunities make CN111867594 a valuable asset if it demonstrates significant therapeutic innovation.

FAQs

1. How does patent CN111867594 differ from similar Chinese pharmaceutical patents?

It likely distinguishes itself through unique chemical structures or targeted therapeutic applications, supported by experimental data demonstrating improved efficacy or stability compared to prior art.

2. Can competitors design around this patent?

Potentially, if they develop compounds outside the scope of the claims or adopt alternative synthesis methods, though detailed claim analysis is necessary to confirm.

3. What are the key considerations when assessing the strength of the claims?

Claim language specificity, breadth, and supporting data on novelty and inventive step influence enforceability and robustness.

4. How does the patent landscape in China affect global drug development strategies?

China’s focus on high-quality patent filings and strategic national policies incentivizes domestic innovation and encourages multinational companies to protect their inventions locally or via patent families.

5. What should patent owners monitor post-grant?

Regular landscape updates, potential third-party challenges, expiration timelines, and new filings around similar compounds or indications.


References
[1] Chinese Patent Search Database, CN111867594 Patent Document.
[2] Chinese Patent Law, 2022 Revisions.
[3] China National Intellectual Property Administration (CNIPA), Patent Examination Guidelines.
[4] World Intellectual Property Organization (WIPO), Patent Landscape Reports, Biopharmaceuticals.
[5] Industry analysis reports, "The Chinese Pharmaceutical Patent Landscape," 2022.

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