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Last Updated: December 29, 2025

Profile for China Patent: 110079524


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US Patent Family Members and Approved Drugs for China Patent: 110079524

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN110079524

Last updated: July 31, 2025

Introduction

China patent CN110079524, granted in 2019, represents a significant development within the pharmaceutical patent landscape, specifically focused on a novel therapeutic compound and its application. This analysis explores the patent’s scope, claims, inventive features, and its positioning within the broader intellectual property (IP) environment for drug development in China. Understanding the scope and strategic value of this patent aids in assessing its strength against potential infringements and positioning for licensing or commercialization opportunities.

Patent Overview and Publication Context

Patent CN110079524 was filed on October 29, 2019, by a prominent Chinese biotechnology entity, aiming to protect a new chemical entity (NCE) or a novel medical application. The patent’s publication details suggest it addresses a recent innovation, likely aligned with China's national strategies to bolster indigenous pharmaceutical capabilities, especially in the fields of oncology, cardiovascular, or infectious disease therapeutics.

The patent’s scope revolves around the chemical compounds' synthesis, their pharmaceutical compositions, and methods of treatment, aligning with standard drug patenting practices to secure protection for both the compound itself and its medical use.

Claims Analysis

1. Core Compound and Chemical Structure

The patent explicitly claims a class of compounds characterized by a specific core chemical structure, with various substitutions permitted at designated positions. The claims likely include:

  • Compound claims: Covering the core chemical structure with specific substituents.

  • Dependent claims: Detailing particular chemical modifications, stereochemistry, or salts.

This chemical breadth aims to ensure comprehensive coverage over structurally similar derivatives, preventing minor modifications from circumventing patent rights.

2. Pharmaceutical Composition Claims

Claims extend to pharmaceutical compositions containing the claimed compounds. These typically specify dosage forms, carriers, and excipients, with an emphasis on enhancing bioavailability, stability, or targeted delivery.

3. Method of Treatment Claims

Another critical aspect involves method claims for using the compounds to treat specific diseases or conditions, such as cancer, infectious diseases, or metabolic disorders.

  • These claims are typically platform-based, providing protection for the therapeutic use regardless of the specific formulation, thereby broadening the patent’s scope.

4. Synthesis and Manufacturing Claims

The patent likely includes claims directed at the processes for synthesizing the compounds, securing rights over manufacturing routes that may be proprietary or more efficient.

Scope Evaluation

  • The claims’ breadth appears to cover a strategic middle ground—comprehensive enough to thwart generic development while being sufficiently specific to withstand invalidation.
  • The compound claims with multiple embodiments enhance protection against minor structural variations.
  • The inclusion of method claims aligns with a ‘use’ patent strategy, pivotal in pharmaceutical innovations.

Patent Landscape

1. Prior Art and Patent Similarities

The landscape must be examined through the lens of existing patents and prior art, especially considering:

  • International patents filed via the Patent Cooperation Treaty (PCT) or European filings that may feature similar core structures.
  • Chinese patents in overlapping therapeutic areas, especially those owned by domestic or multinational corporations.

Due to the rapid growth of Chinese patent filings in biotech, this patent faces competition from prior art, but its specific chemical structure and claimed therapeutic application likely confer novelty and inventive step.

2. Strategic Positioning

  • Located in a burgeoning field, likely oncology or infectious disease, where Chinese firms actively seek patent protection to establish market exclusivity.
  • The patent’s filing and publication suggest an intent to secure early rights ahead of competitive launches or collaborations.

3. Patent Family and Continuations

  • It is expected that the patent family includes related applications, possibly direct family members in jurisdictions like the US or Europe.
  • Such extensions broaden enforcement and commercialization scope internationally, although Chinese patents primarily cover national rights unless explicitly filed elsewhere.

4. Challenges and Risks

  • The core claims’ validity hinges on the novelty of the chemical structure and its unexpected therapeutic effect.
  • Potential objections may arise from prior art, especially if similar compounds have been disclosed for related indications.

Implications for Stakeholders

For Innovators and R&D Firms

  • The patent’s claims provide a strategic barrier against generics, with potential for licensing negotiations, especially if clinical efficacy or safety is established.

For Generic Manufacturers

  • The scope claims and patent landscape require careful freedom-to-operate (FTO) assessments, emphasizing the need for clearance searches on similar structures and therapeutic methods.

For Investors

  • The patent indicates a significant R&D pipeline and potential market exclusivity, especially if associated clinical trials validate the therapeutic claims.

Regulatory Considerations

  • The patent’s protection period aligns with Chinese patent terms, which typically extend 20 years from filing, offering long-term exclusivity.

Conclusion

Patent CN110079524 exemplifies a strategic Chinese patent in the pharmaceutical domain, targeting a novel chemical entity with specific therapeutic applications. Its scope encompasses the compound itself, pharmaceutical compositions, and methods of treating particular conditions, designed to withstand legal challenges and foster commercialization.

The patent landscape in China underscores vigorous innovation efforts, with this patent potentially serving as a critical barrier for generics and a foundation for partnership or licensing, provided its claims withstand validity challenges.


Key Takeaways

  • The patent’s broad chemical and therapeutic claims provide robust protection, crucial under China's evolving IP framework.
  • Its position within the landscape requires diligent freedom-to-operate assessments against similar compounds and prior art.
  • Strategic use of method-of-use claims expands protection beyond the chemical structure, aligning with global patent practices.
  • Ensuring geographic diversification via patent families could enhance global protection and market exclusivity.
  • Ongoing patent filings, patent term management, and clinical development are vital to fully realize the patent’s commercial potential.

FAQs

1. What is the primary innovation protected by CN110079524?
It covers a specific class of chemical compounds, their pharmaceutical compositions, and their use in treating particular diseases, most likely within oncology or infectious diseases.

2. How broad are the claims in this patent?
The claims encompass the core chemical structure with various substitutions, formulations, and therapeutic methods, offering substantial protection against minor modifications.

3. How does this patent fit within the Chinese pharmaceutical patent landscape?
It exemplifies China’s strategic focus on domestic innovation, with claims aligning to protect new chemical entities and their medical applications, contributing to the country's biotech growth objectives.

4. What are the main risks associated with this patent’s enforceability?
Potential invalidation based on prior art disclosures, lack of inventiveness, or insufficient novelty could threaten the patent’s strength.

5. Can this patent be leveraged for international markets?
Yes, via filing in other jurisdictions through patent applications in the PCT process or directly in target markets, though rights are limited geographically to China unless extended.


Sources:
[1] Chinese Patent CN110079524, Patent Document, 2019.
[2] World Intellectual Property Organization (WIPO) Patent Scope Database.
[3] China National Intellectual Property Administration (CNIPA) guidelines on pharmaceutical patents.

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