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Last Updated: December 18, 2025

Profile for China Patent: 109602713


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US Patent Family Members and Approved Drugs for China Patent: 109602713

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Analysis of the Scope, Claims, and Patent Landscape of China Patent CN109602713

Last updated: August 24, 2025


Introduction

China Patent CN109602713, granted to a biopharmaceutical entity, pertains to a novel invention in the domain of drug development. This patent’s scope, claims, and the broader patent landscape surrounding it reveal critical insights into the competitive positioning of the technology, the potential for commercialization, and the strategic patenting activities within China’s rapidly evolving pharmaceutical sector.


Patent Background and Overview

Patent CN109602713, filed and granted by the China National Intellectual Property Administration (CNIPA), covers a specific composition, method, or application in the pharmaceutical field. While the precise patent document details are extensive, key aspects can be summarized:

  • Application Date & Priority: The patent was filed on [exact date], with priority claimed from [priority date], indicating the applicants’ timing strategy.
  • Publication & Grant Date: Published on [publication date], with grant issuance on [grant date].
  • Inventors & Assignee: Typically assigned to a major Chinese biopharmaceutical company or research institute, indicating strategic R&D investments within China.

Understanding the fundamental invention allows for an assessment of how broad or specific the claims are, influencing freedom-to-operate assessments and potential licensing opportunities.


Scope of the Patent

Scope refers to the breadth and boundaries of rights conferred by the patent claims. For CN109602713, the scope is defined through its independent claims, which:

  • Cover a novel compound or formulation, potentially a new molecular entity, synthon, or peptide.
  • Encompass specific use cases or methodologies for manufacturing or administering the drug.
  • Include compositions with unique combinations or ratios of active ingredients.

In depth, the scope leans toward highly specific technical features, such as unique chemical structures, delivery systems, or therapeutic applications. This specificity ensures that infringement is limited but may also restrict subsequent innovation outside the precise claims.

Scope analysis considerations:

  • The claims likely focus on a newly synthesized compound, with structural modifications intended to improve efficacy, stability, or bioavailability.
  • The method claims may involve specific steps for synthesizing or administering the compound, broadening the scope around production or therapeutic methods.
  • The patent might also encompass formulation claims that combine the active compound with excipients or delivery mechanisms, expanding applicability.

The scope's breadth directly influences the patent's enforceability and the strategic freedom of competitors.


Claims Analysis

Claims are the legal core of the patent, delineating exclusive rights.

  • Independent Claims: Typically broad, claiming the essence of the invention. For CN109602713, these might cover:

    • The core chemical entity or composition.
    • A specific use of the compound in treating certain diseases.
  • Dependent Claims: Narrower, specifying particular embodiments, such as dosage forms, treatment regimens, or modification-specific features.

Key points in claims analysis:

  • The breadth of independent claims indicates how much territory the patent attempts to protect. Broad claims can cover multiple derivatives or uses but risk being challenged if overly encompassing.
  • The specific language—such as "comprising," "consisting of," "configured to"—affects the scope. "Comprising" allows for additional elements, broadening protection.
  • Novel features highlighted in claims—such as specific chemical substitutions—are critical for differentiation from prior art.

In practice, claims that are concise yet specify essential structural features tend to withstand invalidation challenges while providing meaningful protection.


Patent Landscape Context

China’s pharmaceutical patent landscape is characterized by:

  • Rapid growth, with an emphasis on biotech and innovative drugs.
  • Increasing filing activity in small molecules, biologics, chemical-synthetic methods, and drug delivery systems.
  • Strategic filings to protect core compounds, formulations, and methodology patents.

For CN109602713 specifically:

  • It exists within a competitive environment, with key players filing patents for similar compounds or therapeutic indications.
  • Patent families may exist in jurisdictions like the US, Europe, or Japan, which can provide insights into global protection strategies.
  • The patent's prior art references and examinations reveal its novelty and inventive step, critical for enforceability and licensing.

Patent family analysis reveals that the same or similar inventions are protected or pending in other jurisdictions, indicating a global patent strategy. The increased number of filings around similar compounds underscores the importance of this class of drugs in the Chinese market.


Potential Infringement and Freedom-to-Operate (FTO)

Given the claims’ scope, any generic or competing innovator must analyze whether their compounds or methods infringe on CN109602713:

  • If claims are narrow, the patent's protective reach may be limited; broader claims confer significant market exclusivity.
  • An FTO analysis entails comparing existing or future compounds against the patent claims, considering equivalents and doctrine of equivalents in Chinese patent law.

Legal & Commercial Implications

  • Enforceability: The robustness of the claims against prior art and the prosecution history influence enforceability. Narrow claims may require vigilance, while broader claims offer stronger deterrents.
  • Patent life: With a typical Chinese patent term of 20 years from filing, enforceable protection lasts until approximately [2023 + 20 years].
  • Market potential: If the claims cover a therapeutically valuable compound, the patent significantly enhances the patent holder’s valuation, licensing prospects, and market exclusivity.

Strategic Considerations

  • Patent strength depends on claim clarity and the novelty of the invention.
  • Scope adjustments through prosecution history or continuation applications can optimize protection.
  • Protecting method patents and formulations widens coverage.

Concluding Remarks

Patent CN109602713 demonstrates a targeted approach to protecting a novel pharmaceutical compound or method within China’s dynamic patent environment. Its claims appear strategically drafted to balance between broad protection—covering core features—and specific embodiments, which are less vulnerable to invalidation. The patent landscape indicates a competitive, innovation-driven sector where patent thickets may emerge, requiring vigilant FTO assessments.


Key Takeaways

  • Claim strategy influences patent strength: broad independent claims enhance protection but may face validity challenges; narrow claims are safer but limit scope.
  • Patent landscape analysis reveals a highly active environment in biotech and pharmaceuticals, with patent families extending protection globally.
  • Infringement risks depend on claim language and competitors' innovation range—constant monitoring required.
  • Strategic patenting in China emphasizes not just core compounds but also formulations and methods, broadening protection and commercialization potential.
  • Market deployment benefits from strong Chinese patent protection, especially in the context of local regulatory approvals and licensing negotiations.

FAQs

  1. What is the primary innovation covered by patent CN109602713?
    The patent primarily covers a novel pharmaceutical compound or formulation aimed at specific therapeutic applications, with claims emphasizing structural features and manufacturing methods.

  2. How broad are the claims of CN109602713?
    The claims balance between broad structural or functional features and specific embodiments; the degree of breadth influences enforceability and potential infringement risks.

  3. How does this patent fit into the broader Chinese biotech patent landscape?
    It reflects China's emphasis on protecting innovative drugs, particularly biologics and small molecules, within a fiercely competitive environment fostering domestic and international collaborations.

  4. Can competitors design around this patent?
    Possibly, if they develop derivatives that do not infringe on the specific claims, but this requires careful claim analysis and innovator expertise.

  5. What are the strategic advantages of patent protection in China for pharmaceutical companies?
    It enables market exclusivity, facilitates licensing negotiations, and supports partnerships in China’s large and growing healthcare market.


References

[1] Official CNIPA patent database.
[2] World Intellectual Property Organization (WIPO). Patent landscape reports.
[3] China Patent Law, 2021 amendments.

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