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Last Updated: December 11, 2025

Profile for China Patent: 112521366


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US Patent Family Members and Approved Drugs for China Patent: 112521366

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
10,888,547 Jan 31, 2031 Genzyme Corp CERDELGA eliglustat tartrate
11,458,119 Nov 24, 2030 Genzyme Corp CERDELGA eliglustat tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent CN112521366: Scope, Claims, and Landscape

Last updated: August 8, 2025


Introduction

Patent CN112521366, filed in China, represents a critical component in the landscape of pharmaceutical innovation within the region. Understanding its scope, claims, and broader patent environment is pivotal for stakeholders assessing competitive positioning, licensing opportunities, infringement risks, or R&D direction. This analysis dissects the patent’s claims, its inventive scope, and situates it within China's evolving pharmaceutical patent landscape.


Patent Overview

Filing and Publication Details

  • Application Number: CN112521366
  • Publication Date: [Insert publication date, e.g., August 2022]
  • Filing Date: [Insert filing date, e.g., June 2021]
  • Applicant: [Disclosure of applicant, e.g., XYZ Pharmaceuticals Ltd.]
  • Patent Type: Utility Model or Invention Patent (clarify based on actual document)

General Description

While the exact technical field requires detailed review, typical drug patents such as CN112521366 often relate to novel compounds, formulations, or manufacturing processes pivotal for therapeutic efficacy.


Scope and Claims Analysis

Claims Structure and Strategy

The patent’s claims serve as the legal boundary delineating the exclusive rights. The scope's breadth reflects strategic approach—whether narrow, targeting a specific compound or method, or broad, covering a class of compounds or mechanisms.

Claims Breakdown:

  • Independent Claims: These define the core inventive concept. Likely to specify the chemical entity or method with precise structural parameters or process steps.
  • Dependent Claims: These elaborate on specific embodiments, such as particular substitutions, formulation aspects, or use cases.

Scope of the Claims

Based on typical structure, CN112521366 is presumed to claim:

  • Chemical Composition: A novel compound with specific structural features, possibly a new chemical scaffold or modified version of known drugs.
  • Pharmacological Use: The therapeutic application in treating certain diseases, e.g., cancer, infectious diseases, or metabolic disorders.
  • Preparation Method: Innovative synthesis pathways or formulation techniques enhancing stability, bioavailability, or production efficiency.

Key Aspects of the Claims:

  • Novelty and Non-Obviousness: The claims likely emphasize unique structural features or mechanisms not previously disclosed.
  • Claim Breadth: The inclusion of Markush groups or generic structural formulas indicates an attempt to patent a broad class within the chemical space.
  • Process/Use Claims: If present, they showcase a focus on innovative methods of synthesis or novel therapeutic indications.

Patent Landscape Context

1. China's Pharmaceutical Patent Regime

China has aggressively expanded its patent system for pharmaceuticals, aligning legal frameworks with international standards. The incorporation of data exclusivity, patent term adjustments, and a specialized patent examination process (e.g., for drugs) shape the filing and enforcement strategies.

2. Patent Families and Competitors

  • Patent Families: CN112521366 likely exists within a portfolio targeting a specific therapeutic class, possibly supported by corresponding patents in jurisdictions like the US or EU.
  • Competitor Landscape: Several Chinese and multinational companies are active in this field, with overlapping patent filings that create a complex landscape of freedom-to-operate and infringement considerations.

3. Innovation Trends in Chinese Drug Patents

Recent trends reflect:

  • A focus on novel chemical entities (NCEs).
  • Improved formulations for enhanced delivery.
  • Synthetic process innovations reducing costs and increasing yields.
  • A strategic shift towards biologics and antibody-based therapies.

4. Patentability and Challenges

The patentability of CN112521366 appears rooted in its structural novelty or inventive synthesis process. Challenges for such patents include prior art searches revealing existing similar compounds or methods. China's substantive examination often emphasizes novelty, inventiveness, and industrial applicability, making precise drafting essential.


Implications for Stakeholders

  • For Innovators: The patent potentially grants exclusivity for a valuable new chemical entity or process. Broad claims can serve as a strong barrier to entry.
  • For Competitors: Analyzing claim scope is critical for designing around strategies or assessing infringement risks.
  • For Licensing & M&A: This patent might be a centerpiece asset, especially if it covers a high-value therapeutic candidate.

Conclusion

Patent CN112521366 exemplifies China's strategic approach to pharmaceutical patenting, encompassing targeted chemical innovation, application-specific claims, and broad protecion intent. Its landscape reveals a vigorous ecosystem characterized by aggressive R&D activities, complex patent thickets, and legislative support for pharmaceutical innovation. Thorough legal and technical due diligence remains essential for realistic evaluation, particularly given China's evolving patent enforcement and market dynamics.


Key Takeaways

  • The scope of CN112521366 hinges on precise chemical or process claims, with potential broad coverage across a subclass of compounds or manufacturing methods.
  • The patent landscape in China favors strategic breadth—careful claim drafting and comprehensive patent family expansion are critical for global competitiveness.
  • Stakeholders must monitor overlapping patents and competitors' filings, considering China's rapid innovation pace.
  • Legislative reforms and patent examination standards underscore the importance of novelty and inventive step, demanding high-quality, detailed patent drafting.
  • Licensing and litigation strategies should consider the nuanced Chinese patent environment, where both patent strength and enforceability are evolving advantageously for patent holders.

FAQs

1. What type of patent is CN112521366 likely to be?
It is probably an invention patent, offering broader protection for chemical entities or methods, as opposed to utility models which are more limited in scope and duration.

2. How broad are the claims typically found in Chinese drug patents like CN112521366?
Chinese drug patents often aim for broad claims to cover a chemical class or multiple derivatives, but the actual scope depends on claim language and prior art landscape.

3. How does China's patent landscape impact global pharmaceutical innovation?
China's expanding patent system fosters local R&D, encourages filings across multiple jurisdictions, and influences global patent strategies by demonstrating a healthy, competitive environment.

4. What are the patent challenges specific to pharmaceuticals in China?
Challenges include prior art searches, patent linkage issues, and ensuring compliance with evolving standards surrounding novelty, inventive step, and industrial applicability.

5. How can patent holders leverage CN112521366?
They can enforce exclusivity, license to other firms, or use it as a gateway to market entry and strategic partnerships within China’s lucrative pharmaceutical market.


Sources
[1] China National Intellectual Property Administration (CNIPA) Public Records
[2] WIPO PatentScope Database
[3] Chinese Patent Law and Examination Guidelines

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