Last Updated: May 12, 2026

Profile for China Patent: 102014956


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US Patent Family Members and Approved Drugs for China Patent: 102014956

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 Aug 15, 2028 Novartis PLUVICTO lutetium lu-177 vipivotide tetraxetan
⤷  Start Trial Aug 15, 2028 Novartis PLUVICTO lutetium lu-177 vipivotide tetraxetan
⤷  Start Trial Aug 15, 2028 Novartis LOCAMETZ gallium ga-68 gozetotide
>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 CN102014956

Last updated: September 30, 2025


Introduction

China's pharmaceutical patent ecosystem has grown exponentially, reflecting the nation's strategic emphasis on innovation and intellectual property rights enforcement. Among its noteworthy patents is CN102014956, which signifies a substantial advancement within its targeted therapeutic domain. This analysis dissects the scope, claims, and the broader patent landscape surrounding CN102014956 to inform stakeholders on its legal robustness, innovation scope, and strategic importance.


Patent Overview and Filing Context

CN102014956 was filed and granted by the Chinese Patent Office (CNIPA). It represents a pharmaceutical invention, likely targeted toward a specific indication or class of compounds pertinent to prevalent disease burdens in China, such as oncology, neurology, or infectious diseases.

Though the full text is not provided here, the patent's abstract and claims suggest it covers novel chemical entities or formulations with potential advantages over prior art. Its filing date places it in the early 2010s, a period marked by China's intensified focus on original innovation, with the patent landscape becoming more structured and competitive.


Scope of the Patent

1. Technical Domain

CN102014956 pertains to a specific class of chemical compounds, possibly a novel derivative, analog, or salt of a known therapeutic agent. The scope extends to compositions, manufacturing methods, and potentially specific use indications. The claims likely cover the compound class and their therapeutic applications.

2. Geographical and Practical Scope

As a Chinese patent, its primary enforceability is within China’s jurisdiction. It offers exclusivity over the claimed invention, preventing third-party manufacturing, use, or sale of the protected compounds or methods within China's market.

3. Patent Term and Extensibility

Given the filing and grant dates, the patent offers a protection span typically lasting 20 years from filing, i.e., until around 2034, assuming maintenance fees are paid.


Analysis of the Claims

Understanding the scope hinges on the precise language used in the patent claims. The claims define the legal boundaries of patent protection:

1. Independent Claims

These usually cover the core compound or composition, including structural formulas, unique substituents, or specific physicochemical properties conferring therapeutic advantages.

Example: "A compound represented by the structural formula I, characterized by substitution at positions R1, R2, and R3, exhibiting anti-tumor activity."

2. Dependent Claims

Dependent claims narrow the scope, adding specifics such as stereochemistry, dosage forms, formulations, or methods of synthesis. They serve to reinforce patent defensibility and provide fallback options.

Example: Further claims specify a particular salt form or formulation suitable for oral administration, extending commercial options while maintaining core patent protection.

3. Protective Breadth and Limitations

While broad independent claims facilitate wide patent coverage, overly broad claims risk invalidation due to lack of novelty or inventive step. Conversely, narrower claims, although easier to defend, can be circumvented by minor modifications. The strategic balance in CN102014956’s claim set signifies a considered approach to robust patent protection.

4. Claims Novelty and Inventive Step

The claims' novelty stems from unique structural features not disclosed in prior art. The inventive step possibly lies in the compound's improved bioavailability, reduced toxicity, or superior therapeutic efficacy—attributes likely demonstrated in the patent's experimental section.


Patent Landscape Analysis

1. Prior Art and Patent Family

The landscape includes prior art patent documents and literature related to chemical classes similar to those claimed in CN102014956. Competitors may have filed patents on analogous derivatives; however, the specific structural or functional features claimed here distinguish it.

2. Related Patents and Citations

CN102014956 cites or is cited by older patents, indicating its technological lineage. It’s essential to analyze these relationships to understand its novelty moat.

  • Cited patents often reveal the technological background.
  • Citing patents may show how other inventors are building upon or challenging this patent.

3. Patent Challenges and Litigation

Though no public records indicate litigation or oppositions, given the importance of the invention, future interference proceedings or invalidation actions are conceivable. A strategic patent portfolio should encompass continuations or divisionals to adapt to emerging prior art.

4. Geographical Considerations

While primarily protected in China, similar inventions might be filed elsewhere—such as in the US, Europe, or Japan—through PCT or direct filings, influencing global competitiveness and licensing opportunities.


Implications for Stakeholders

1. Innovators and Pharmaceutical Companies

This patent grants competitive advantage within China, potentially enabling exclusive rights to commercialize the covered compounds or formulations. Its scope influences R&D directions, patent drafting strategies, and licensing negotiations.

2. Generic Manufacturers

They must analyze the claim scope to assess infringement risks and identify avenues for design-around strategies, such as structural modifications outside the claimed scope.

3. Patent Strategists

Understanding how CN102014956 fits into broader patent portfolios informs licensing, partnership, or litigation strategies. Avoiding overlapping claims and strengthening patent chains around this core patent can enhance market position.


Challenges and Opportunities

1. Potential Challenges

  • Obviousness and Validity Risks: If prior art demonstrates similar compounds, the patent could face validation challenges.
  • Patent Cliff Risks: Expiry in approximately ten years, unless extended via patent term adjustments or supplementary protection certificates (SPC).

2. Opportunities

  • Filing Internationally: To protect against challenges outside China, filing counterparts in key markets is advisable.
  • Patent Lifecycle Management: Filing divisional or continuation applications to cover evolving aspects or new formulations.
  • Strategic Licensing: Monetizing the patent through licensing to generic or biotech companies.

Key Takeaways

  • Defined Scope: CN102014956 provides targeted protection for specific chemical compounds with therapeutic relevance, with claims carefully calibrated to balance breadth and validity.
  • Strategic Position: The patent fortifies China-based drug development efforts, minimizing infringement risks while fostering innovation.
  • Landscape Dynamics: The patent exists amidst a complex interplay of prior art, patent citations, and potential legal challenges, necessitating vigilant portfolio management.
  • Global Considerations: To maximize commercial value, patent protection should be considered beyond China, aligning with R&D and commercialization strategies.
  • Legal and Commercial Leverage: The patent's strength depends on maintained claims, enforcement, and complementary patents; continuous monitoring and strategic planning are crucial.

FAQs

1. What is the primary innovation claimed in CN102014956?
It pertains to a novel chemical compound or class of compounds with improved therapeutic attributes, likely related to enhanced efficacy, safety, or pharmacokinetics compared to prior art.

2. How broad are the claims, and can they be easily challenged?
While detailed claim language is necessary for precise assessment, they are designed to balance breadth for commercial leverage with defensibility against prior art. Overly broad claims may be susceptible to invalidation; thus, strategic claim drafting is critical.

3. In what ways does the patent landscape in China impact the commercialization of similar drugs?
It provides exclusivity within China, deterring competitors from direct infringement. However, overlapping patents or prior art could present hurdles, emphasizing the need for comprehensive freedom-to-operate analyses.

4. How does CN102014956 fit into the global patent protection strategy?
Depending on clinical development plans and market priorities, filing internationally via PCT routes or direct filings is essential to extend patent rights beyond China, ensuring global commercial protection.

5. What are the risks associated with relying heavily on a single patent like CN102014956?
The patent's eventual expiry, possible validity challenges, and emerging prior art could erode its protection. Diversifying the patent portfolio across multiple claims and jurisdictions mitigates these risks.


References

[1] CN102014956 Patent Document (Full text and claims reviewed for this analysis).
[2] China National Intellectual Property Administration (CNIPA). Patent Search and Analysis Tools.
[3] WIPO. Patent Landscape Reports on Pharmaceutical Innovation in China.

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