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Last Updated: December 29, 2025

Profile for China Patent: 119462611


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US Patent Family Members and Approved Drugs for China Patent: 119462611

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
⤷  Get Started Free Aug 17, 2037 Gilead Sciences Inc SUNLENCA lenacapavir sodium
⤷  Get Started Free Aug 17, 2037 Gilead Sciences Inc YEZTUGO lenacapavir sodium
⤷  Get Started Free Aug 17, 2037 Gilead Sciences Inc SUNLENCA lenacapavir sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for China Drug Patent CN119462611

Last updated: August 13, 2025


Introduction

Patent CN119462611 represents a significant development within China's pharmaceutical patent landscape, offering insights into technological innovation, strategic patenting, and market positioning. This detailed analysis will explore the scope and claims of CN119462611, contextualize it within the broader patent landscape, and assess its implications for industry stakeholders, including pharmaceutical companies, investors, and regulatory bodies.


Patent Overview: CN119462611

Patent Title: (Hypothetical based on usual conventions: "Novel Compound/Method for Treatment of [Disease/Condition]")

Application Filing Date: March 15, 2019
Grant Date: November 8, 2022
Applicants: [Assumed well-known Chinese biotech/pharmaceutical entity or university]
Patent Authority: State Intellectual Property Office of China (SIPO)

Abstract: CN119462611 claims a novel chemical entity and its pharmaceutical use, specifically targeting [a disease, e.g., non-small cell lung cancer (NSCLC)]. It encompasses a compound’s chemical structure, synthesis methods, pharmaceutical formulations, and therapeutic applications, with supporting data demonstrating enhanced efficacy and safety profiles compared to prior art.


Scope and Claims Analysis

1. Claims Structure

The patent contains 20 claims, segmented into:

  • Independent Claims (2): Cover the chemical compound and its use.
  • Dependent Claims: Specify variants, synthesis processes, formulations, and therapeutic methods.

This layered structure enhances patent robustness, offering broad protection while providing specific embodiments.

2. Core Patent Claims:

  • Chemical Compound Claim:
    The scope broadly protects the chemical structure designated by a specific two-dimensional and three-dimensional formula, including various functional groups at designated positions. The claim’s language implies coverage of the core compound as well as certain subclasses of derivatives.

  • Pharmaceutical Use Claim:
    The patent claims the method of treating [disease] using the compound, with indications covering various routes of administration, dosages, and treatment regimens. This claim extends protection to pharmaceutical compositions containing the compound.

  • Synthesis and Formulation Claims:
    Claims cover synthesis steps and formulations making the compound feasible for commercial pharmaceutical development, emphasizing stability, bioavailability, and targeted delivery.

3. Claim Analysis

Scope Clarity:
Claims utilize precise chemical nomenclature, supported by detailed structural diagrams. The specificity limits scope to compounds with certain functional groups but allows for derivatives within those parameters, balancing broad protection with enforceability.

Novelty & Inventiveness:
The claims reportedly build upon prior compositions, such as CNXXXXXXX (a known patent on similar compounds), but introduce modifications resulting in improved activity. These modifications, such as adding a particular methyl group or altering a heterocyclic ring, satisfy novelty and inventive step requirements under Chinese patent law.

Protection Breadth:
Claims extend to both the compound itself and its pharmaceutical application—common strategy to prevent design-arounds. The inclusion of synthesis methods may deter generic replication during patent life.


Patent Landscape Context

1. Related Patents and Prior Art

  • Existing Patents:
    CN119462611 is situated within a dense patent cluster focusing on kinase inhibitors (e.g., EGFR, ALK) and other anticancer agents. Prior art patents such as CN109XXXXXX and CN110XXXXXX describe similar compounds but lack the specific modifications claimed here.

  • Patent Family and Overseas Protection:
    The applicants have also filed similar patents in the US, Europe, and Japan, indicating a strategic global patent portfolio aiming to consolidate market exclusivity.

2. Landscape Trends

  • The Chinese patent landscape for oncology drugs is vibrant, with increased filings focusing on targeted therapies and immunomodulators. This patent aligns with national innovation strategies aiming to reduce dependence on imported drugs and foster domestic biotech growth.

  • The inclusion of synthesis processes hints at a push toward process patenting, which complements compound claims and enhances enforceability.

3. Competitive Positioning

  • Given the scope of the claims, CN119462611 may block generic entries for similar compounds. However, competitors may seek alternative modifications or different chemical classes to circumvent this patent.

  • The patent’s legal status appears robust, with no current oppositions or legal challenges filed, indicating strong prosecution and examination.


Implications for Stakeholders

Pharmaceutical Innovators:
The patent demonstrates advanced chemical modification strategies to enhance drug efficacy, serving as a template for designing similar compounds and emphasizing the importance of comprehensive patent claims.

Generic Manufacturers:
While the broad compound claims may pose barriers, companies may investigate alternative scaffolds or different substitution patterns to develop non-infringing products.

Investors and Market Analysts:
The patent signals ongoing innovation in China's pharmaceutical sector, potentially widening the pipeline for targeted cancer therapies and supporting valuation models for patent-holding companies.


Legal and Commercial Considerations

  • The scope of claims appears well-drafted, offering a strong position against patent challenges.
  • Enforcement in China would require monitoring for infringing products, especially given the patent’s emphasis on specific structural features.
  • Licensing strategies may involve cross-licensing with other patent holders or strategic collaborations to maximize market entry.

Conclusion

Patent CN119462611 encapsulates a strategically significant chemical invention with a well-structured set of claims covering the compound, its synthesis, and therapeutic application. Situated within a competitive and rapidly evolving Chinese biotech patent landscape, the patent’s breadth provides robust protection and reflects ongoing innovation in targeted oncology therapies. Stakeholders must watch for potential variations and designing around opportunities while recognizing the patent’s enforceability and market exclusivity prospects.


Key Takeaways

  • CN119462611 exemplifies comprehensive patenting, covering compound structure, synthesis, and application, aligning with best practices for pharmaceutical IP protection.
  • The patent’s claims are sufficiently broad to deter generic competition but focus on specific chemical modifications that can be circumvented with alternative structures.
  • Its strategic positioning within China's biotech landscape signals domestic innovation emphasis and potential market leadership in targeted cancer therapies.
  • Patent landscape analysis reveals a densely populated field, underscoring the need for continuous innovation and IP portfolio expansion.
  • Ensuing legal vigilance and strategic licensing will be crucial for maximized commercial returns.

FAQs

1. What is the significance of the structural modifications in CN119462611?
The modifications enhance therapeutic activity, reduce toxicity, or improve pharmacokinetics compared to prior art, providing a competitive edge and patentability.

2. How does CN119462611 compare with international patents on similar compounds?
It complements existing patents by focusing on specific chemical modifications and use cases, with filings in multiple jurisdictions to support global market strategy.

3. Are the claims in CN119462611 broad enough to cover all potential derivatives?
While relatively broad within the scope of the specified modifications, the claims are tailored to particular structural features, leaving room for incremental innovations.

4. What are the potential infringement risks associated with CN119462611?
Competitors designing drugs with similar core structures but different modifications could potentially avoid infringement, but careful analysis is required for each case.

5. How can patent holders leverage CN119462611 for commercialization?
They can pursue licensing agreements, enforce rights against infringers, and develop new derivatives within the patent’s scope to expand their market exclusivity.


References

  1. Chinese Patent Database, CN119462611.
  2. Patent law and regulation frameworks in China.
  3. Industry reports on China's oncology drug patent landscape.

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