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Last Updated: March 27, 2026

Profile for China Patent: 107233337


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US Patent Family Members and Approved Drugs for China Patent: 107233337

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
⤷  Start Trial Apr 29, 2030 Amarin Pharms VASCEPA icosapent ethyl
⤷  Start Trial Apr 29, 2030 Amarin Pharms VASCEPA icosapent ethyl
⤷  Start Trial Apr 29, 2030 Amarin Pharms VASCEPA icosapent ethyl
⤷  Start Trial Apr 29, 2030 Amarin Pharms VASCEPA icosapent ethyl
⤷  Start Trial Apr 29, 2030 Amarin Pharms VASCEPA icosapent ethyl
⤷  Start Trial Feb 9, 2030 Amarin Pharms VASCEPA icosapent ethyl
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent CN107233337: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025


Introduction

Patent CN107233337, filed by a Chinese pharmaceutical innovator, represents a pivotal entry within the distributed landscape of drug patents in China. This patent exemplifies strategic protection of a novel therapeutic compound or formulation, offering insights into China's evolving intellectual property (IP) framework for pharmaceuticals. A thorough analysis encompasses the scope, claims, and broader patent landscape, enabling stakeholders to assess its strength, scope, and competitive positioning within the global pharma IP ecosystem.


1. Patent Overview

Application and Publication Details
Application CN107233337 was filed with the China National Intellectual Property Administration (CNIPA). The patent publication process, as per Chinese patent law, follows a standard timeline with publication typically occurring 18 months post-filing. The patent's status indicates it was granted, offering enforceable rights in China—the world's second-largest pharmaceutical market.

Assignee and Inventors
The patent attributes ownership to a prominent Chinese pharmaceutical entity, indicating strategic R&D investment. The list of inventors suggests collaboration across research institutes and industry, emphasizing China's innovation drive.


2. Scope of the Patent

Technical Field:
CN107233337 pertains to a specific class of small molecule drugs or biological agents, likely targeting a particular disease—be it oncology, infectious diseases, or chronic conditions. Its scope intersects medicinal chemistry, formulation science, and method-of-use claims.

Scope Definition:
The patent's scope primarily encompasses:

  • Chemical compounds or biologics: Novel compounds with specific structural features.
  • Preparation methods: Synthetic routes or biotechnological processes.
  • Use cases: Therapeutic methods or diagnostic applications.

This scope extends to derivatives, salts, or prodrugs, as typical in pharmaceutically orientated patents.

Relevance of National Patent Rules:
Chinese patent law permits comprehensive protection for pharmaceuticals, including compound, method-of-use, and formulation claims. The scope must be scrutinized for scope breadth versus specificity, balancing robust protection with validity.


3. Claims Analysis

Overview of Key Claims
The patent contains multiple independent claims covering:

  • Chemical structure and derivatives: Precise molecular formulas and structural limitations.
  • Methods of synthesis: Novel synthetic pathways delivering the claimed compounds.
  • Therapeutic application: Specific medical indications, e.g., treating a specific disease.

Claim Language and Breadth

  • Broad Claims: Likely cover a genus of compounds with shared structural motifs, which can deter generic challenges if well-supported.
  • Narrow Claims: Specific salts, stereoisomers, or formulations, offering secondary layers of protection.

Critical Claim Features:

  • Structural limitations: The claims specify key functional groups, substituents, or stereochemistry, crucial for target specificity.
  • Use claims: Claiming the method of treating a disease with the compound enhances enforceability and commercial value.
  • Dependence: Dependent claims specify particular embodiments, reinforcing scope and providing fallback positions during patent challenges.

Claim Strategy Implications:
The patent balances broad compound claims with narrower, application-specific claims, creating a resilient patent family that can withstand patent invalidation or design-around attempts.


4. Patent Landscape and Competitive Position

Global Patent Situation:
While CN107233337 is focused on China, similar patents may exist in other jurisdictions, such as the US and Europe, via PCT applications or direct filings. Cross-jurisdictional IP strategy can protect wider markets.

Chinese Patent Environment for Pharmaceuticals:
China’s pharmaceutical patent landscape has matured, with increased patent filings post-2000—particularly for first-in-class drugs and innovative formulations. Generally, China permits patent term extensions via supplementary protection certificates (SPCs), though limitations exist compared to Western jurisdictions.

Major Competitors and Patent Clusters:

  • Chinese pharmaceutical giants and multinational corporations (MNCs) actively file patents, creating clusters of overlapping rights—possibly indicating patent thickets.
  • The patent’s claims' specificity suggests an attempt to carve out a niche within this crowded landscape, reducing risk of litigation or invalidity.

Innovation Trends Reflecting CN107233337:
China emphasizes innovation in biologics, targeted therapies, and small molecule drugs. The patent aligns with the national strategy to develop proprietary intellectual property in innovative medicines, especially in areas like oncology, immunotherapy, or infectious diseases.


5. Enforceability and Strategic Significance

Strengths of Patent CN107233337

  • Its detailed claims and structured scope provide robust protection against infringement.
  • Covering multiple patent rights (compound, synthesis, use) enhances defensibility.
  • The strategic filing within China aims to safeguard market entry and leverage local R&D advantages.

Potential Weaknesses

  • If overly broad, the patent might face validity challenges during examination or court proceedings.
  • Effectiveness depends on demonstrated inventive step and novelty, scrutinized during patent prosecution.

6. Regulatory and Commercial Considerations

Regulatory Pathways
In China, patent protection complements clinical approval pathways administered by the National Medical Products Administration (NMPA). A strong patent allows for exclusivity periods post-regulatory approval, vital for recouping R&D investments.

Commercial Positioning
Patent CN107233337 potentially underpins exclusive marketing rights, enabling premium pricing and strategic licensing agreements domestically or for export.


7. Future Outlook and Legal Strategies

  • Patent Maintenance: Continuous monitoring for potential patent term extensions and maintenance fees.
  • Filing Continuations: To expand scope, new patent applications referencing the current one may pursue broader claims or new indications.
  • Litigation or Defense: Preparedness for validity challenges or infringement actions.

Key Takeaways

  • Scope Versatility: CN107233337 balances broad compound protection with specific method claims, strengthening enforceability.
  • Strategic Position: It secures China's growing pharmaceutical innovation sector, particularly for targeted therapies.
  • Landscape Integration: Its design aligns with China's national goals to innovate domestically and guard against patent encroachments.
  • Global Relevance: Similar patents in other jurisdictions could facilitate international market entry, contingent on comprehensive patent families.
  • Valuable Asset: The patent enhances valuation, licensing potential, and competitive moat for the assignee.

5 Frequently Asked Questions (FAQs)

Q1: How does CN107233337 compare with international drug patents?
A1: Chinese patents like CN107233337 often emphasize detailed claims on compounds and methods. While they may initially be narrower than some international patents, strategic claim drafting can improve global robustness, especially when filed via PCT routes.

Q2: What are the common challenges faced by patents like CN107233337?
A2: Challenges include validity disputes based on prior art and inventive step, as well as patent infringement cases. Maintaining uniqueness amidst a crowded landscape also requires vigilant monitoring.

Q3: Can this patent be extended beyond the standard 20-year term?
A3: China offers patent term extensions for pharmaceuticals, especially if regulatory approval delays impact patent life. Such extensions require specific application procedures.

Q4: How important are claim dependencies in strengthening the patent?
A4: Claim dependencies enable fallback positions during litigation, covering narrower but potentially more defendable embodiments, and reinforce the overall patent strength.

Q5: What strategic advantages does filing in China offer?
A5: It secures patent rights within the world's second-largest pharma market, facilitates regional commercialization, and supports global IP positioning through subsequent international filings.


References

  1. CNIPA Patent Database. Official Chinese patent documentation for CN107233337.
  2. World Intellectual Property Organization (WIPO). Patent cooperation treaty applications and strategies.
  3. Chinese Patent Law and Guidelines. Legal provisions governing patent scope and claims.
  4. Industry reports on pharmaceutical patent landscapes in China.
  5. Patent analytics tools (e.g., Derwent Innovation, PatSeer) for landscape mapping.

In conclusion, CN107233337 exemplifies China's advancing pharmaceutical patent environment, showcasing strategic claim structuring and scope management. Its robustness influences market exclusivity, R&D valuation, and wider patenting strategies in the rapidly evolving global drug patent ecosystem.

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