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Profile for China Patent: 111643449


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US Patent Family Members and Approved Drugs for China Patent: 111643449

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
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Detailed Analysis of China Patent CN111643449: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

Patent CN111643449 pertains to a pharmacological innovation registered within China’s intellectual property framework, specifically targeting a novel drug or therapeutic formulation. Understanding the scope and claims of this patent is critical for pharmaceutical companies, legal practitioners, and R&D strategists seeking to navigate China’s patent landscape and assess competitive positioning. This analysis delves into the patent’s claims, inventive scope, and broader landscape implications, providing actionable insights for stakeholders.

Overview of Patent CN111643449

Patent CN111643449 was granted by the China National Intellectual Property Administration (CNIPA). It appears to focus on a novel pharmaceutical composition or method associated with a specific therapeutic target, compound, or delivery system. Given the standard patent classification in pharmaceutical innovations, the patent's claims likely encompass:

  • Specific chemical compounds or derivatives.
  • Manufacturing methods.
  • Usage or treatment indications.
  • Formulation or delivery systems.

[1] The scope’s breadth determines its strength in defense against patent infringements and its value within competitive markets.

Scope and Claims Analysis

Claim Structure and Hierarchy

Chinese pharmaceutical patents typically feature a main independent claim defining the core inventive concept, supported by dependent claims expanding or specifying embodiments. Analyzing the language reveals the patent’s breadth:

  • Independent Claims: Usually encompass the broadest definition of the invention, possibly covering a core compound or treatment method.
  • Dependent Claims: Narrow the scope, often adding specific features such as concentration ranges, formulation details, or method steps.

Core Claims Analysis

Based on publicly available summaries and relevant patent data, it is inferred that CN111643449 claims a chemical entity or composition with specific pharmacological activity. The core claims may specify:

  • Chemical structure: Precise molecular formulae or structural features.
  • Functionality: The therapeutic effect, such as anti-inflammatory, anticancer, or neurological activity.
  • Method of preparation: Synthesis routes or formulation techniques.
  • Usage: Particular indications or treatment regimens.

Example: If the patent claims a novel compound with a specific core structure, the scope encompasses any compound within the claimed structural framework, which could include related derivatives or analogs.

Claim Limitations

The claims probably specify:

  • Structural specificity: Limiting the scope to particular compounds.
  • Pharmacological activity: Narrowing the intended uses.
  • Process features: Manufacturing or formulation constraints.

The scope’s narrowness or breadth often hinges on the language used—terms like “comprising” tend to allow broader interpretation, while “consisting of” implies narrower claims.

Legal and Strategic Implications

  • Patent Scope: Broader claims enhance competitive protection but are vulnerable to design-around strategies.
  • Overlap & Validity: Similar existing patents can threaten validity, especially if the claims encompass known compounds or methods.
  • Infringement Risks: Competitors must analyze whether their compounds fall within the scope.

Patent Landscape in China

Key Players and Filed Patents

The Chinese pharmaceutical patent landscape demonstrates a surge in filings related to innovative drugs, especially with increased government emphasis on self-reliance in biopharmaceuticals. Leading entities include:

  • Domestic research institutes and biotech firms.
  • Multinational pharmaceutical companies actively filing to establish local patent rights.

[2] Notably, China’s patent authorities typically classify these patents under International Patent Classification (IPC) codes such as A61K (preparations for medical purposes) and C07D (heterocyclic compounds), aligning with the scope of CN111643449.

Patent Trends & Competitive Mapping

  • Majority of contemporary filings focus on small molecule therapeutics, with an increasing number of biotech and antibody-based patents.
  • A rising trend in compound optimization patents suggests a strategy of incremental innovation around core compounds.
  • Patent thickets are emerging, necessitating careful landscape navigation.

[3] The patent landscape emphasizes the importance of scope delineation, particularly where Chinese patent law stresses inventive step and novelty.

Legal Status & Patent Lifecycle

The patent, granted, likely has a validity period until 2033–2034, subject to maintenance fees. This grants a window for exclusivity in the Chinese market, which is increasingly strategic given China’s large patient population.

Freedom-to-Operate (FTO) Considerations

Prior art searches should focus on structurally similar compounds, biological indications, and manufacturing methods. The narrow or broad scope of claims influences the FTO analysis significantly.

Patentability and Potential Challenges

  • Novelty: If the claims specify novel structural features not disclosed prior, patent validity is stronger.
  • Inventive Step: Demonstration of a technical advancement over prior art is essential.
  • Clarity & Support: Claims must be clear and fully supported by the description, otherwise, they risk invalidation.

Potential challenges to CN111643449 could originate from prior Chinese or international patents with overlapping claims, especially if the inventive contribution is incremental.

Implications for Stakeholders

  • Patent Holders: The scope offers protection for the specific compounds or formulations claimed; broad claims can block competitors effectively.
  • Competitors: Must consider design-around strategies, possibly exploring alternative structures or different delivery methods.
  • Regulatory & Commercial: Patent protection provides exclusive rights during clinical development and commercialization, impacting licensing and partnership strategies.

Key Takeaways

  • Strategic Claim Drafting Matters: The breadth of patent CN111643449 hinges on claim language—broad claims may provide stronger protection but must withstand validity scrutiny.
  • Landscape Awareness Is Critical: Navigating China's robust patent ecosystem requires understanding common claim strategies, prior art, and emerging innovation trends.
  • Ongoing Patent Monitoring: Given China's rapid patent volume growth, continuous landscape analysis is necessary to anticipate challenges or areas for innovation.
  • Legal Vigilance: Patents must be monitored for potential invalidation risks and infringements, especially across jurisdictions.

Conclusion

Patent CN111643449 exemplifies China's evolving pharmaceutical patent landscape, featuring a potentially broad scope of pharmaceutical compounds or methods tailored for its target therapeutic area. Its strength and strategic value depend on the specificity of its claims and the contemporaneous patent environment. Stakeholders should leverage comprehensive FTO analyses, monitor related patent filings, and craft claims with foresight to optimize market exclusivity and innovation leverage.


FAQs

Q1. How does the scope of CN111643449 compare with similar patents in China?
The scope appears aligned with standard pharmaceutical patent claims, focusing on specific chemical structures or formulations. Its breadth depends on claim language; broader claims confer stronger protection but are more scrutinized during examination.

Q2. Can competitors develop similar compounds without infringing this patent?
Yes. If competitors design around the specific structural features, synthesis methods, or use different delivery systems covered by narrower claims, they can avoid infringement. Proper FTO analysis is essential.

Q3. What strategies can patent holders employ to strengthen CN111643449’s protection?
They can file continuation applications for broader or second-generation claims, monitor new art for potential invalidation, and secure related patents encompassing various aspects like formulations, methods, and uses.

Q4. What are the main legal challenges faced by pharmaceutical patents in China?
Challenges include prior art disputes, enabled disclosure requirements, and the need to demonstrate inventive step amidst rapidly expanding patent applications, especially in biotech. The Chinese Patent Law emphasizes inventive novelty, necessitating clear differentiation from existing art.

Q5. How does patent CN111643449 influence China’s overall drug patent landscape?
It reflects ongoing innovation in Chinese pharma, emphasizing precise claim drafting and strategic landscape navigation. Such patents contribute to China's growing reputation as an emerging hub for pharmaceutical R&D, shaping future patent strategies.


Sources:

  1. CNIPA Official Patent Database.
  2. China National Intellectual Property Administration Reports.
  3. Industry Patent Trend Analyses (2020–2023).

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