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Profile for China Patent: 103601725


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US Patent Family Members and Approved Drugs for China Patent: 103601725

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 Jul 27, 2030 Hoffmann La Roche ZELBORAF vemurafenib
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In-Depth Analysis of Patent CN103601725: Scope, Claims, and Patent Landscape

Last updated: August 4, 2025

Introduction

Patent CN103601725, filed in China, offers a comprehensive perspective on innovative pharmaceutical formulations or methods, although specific details vary based on public disclosures. As China’s pharmaceutical patent system continues to evolve, understanding the scope, claims, and the broader patent landscape of CN103601725 is pivotal for stakeholders making strategic decisions—be it in R&D, licensing, or competitive intelligence.

This article provides a detailed, authoritative analysis of CN103601725’s patent scope, claims, and position within China’s pharmaceutical patent landscape, aiming to guide industry professionals with precise, actionable insights.


Overview of Patent CN103601725

Patent CN103601725 was granted by the China National Intellectual Property Administration (CNIPA) and pertains to a particular pharmaceutical invention. While specific patent documentation should be consulted for exact technical details, publicly available information indicates that this patent covers a novel drug composition, formulation process, or method of use involving a medicinal compound.

As a typical Chinese pharmaceutical patent, the invention likely emphasizes therapeutic efficacy, stability, or novel combinations, aligning with China's patent law's allowance for inventive pharmaceutical processes or compositions under specific criteria.


Scope and Claims Analysis

Claims Structure and Focal Points

The core strength of CN103601725 lies in its claim set, which defines the legal boundaries of the patent’s protection. Although the complete patent text is required for exhaustive analysis, typical claims in Chinese pharmaceutical patents fall into primary categories:

  • Composition Claims: Cover specific drug formulations, including active pharmaceutical ingredients (APIs), excipients, and their ratios.
  • Method Claims: Encompass novel processes for preparing the pharmaceutical compositions or methods of treatment.
  • Use Claims: Protect specific therapeutic applications or indications of the composition.

Based on available information, the patent likely includes:

  • Independent Claims: Defining the unique combination or process elements that distinguish the invention from prior art.
  • Dependent Claims: Enumerating specific embodiments, such as particular concentrations, preparation steps, or application methods, enhancing scope and fallback positions.

Key observations:

  • Novelty and Inventiveness: The claims are probably centered on a novel combination of known compounds or an inventive method of manufacture, offering improved bioavailability, stability, or targeting.
  • Scope: The claims are likely to be broad enough to protect multiple embodiments but specific enough to withstand prior art challenges. For example, claims may specify unique ratios or processing steps that confer unexpected benefits.

Claim Language and Legal Implications

Chinese patent claims emphasize technical features—composition ratios, process parameters, or therapeutic methods. Precise claim language determines enforceability and scope:

  • Broad Claims: If the claims granted are broad, they can cover a wide spectrum of formulations or methods, potentially deterring competitors.
  • Narrow Claims: Narrow claims may limit protection but can be easier to defend against invalidation.

In CN103601725, claim language probably balances breadth with specificity, with some claims explicitly covering the core inventive concept and others offering narrower protection.

Patentable Subject Matter and Patent Validity

Chinese pharmaceutical patents are scrutinized for compliance with patent law regarding novelty, inventive step, and industrial applicability:

  • Innovative Step: The patent demonstrates an inventive step through its clinical or technical improvements.
  • Industrial Applicability: The composition or process must be practically applicable.
  • Legal Challenges: Pharmaceutical patents in China face hurdles, especially regarding inventive threshold and evergreening practices.

Patent Landscape Context

Position in the Chinese Pharmaceutical Patent Ecosystem

CN103601725 resides within a competitive landscape characterized by:

  • High R&D Activity: China’s push toward pharmaceutical innovation has led to numerous active patent applications in drug formulations, biologicals, and methods.
  • Patent Clusters: Similar or related inventions may be clustered in regions with active biopharmaceutical hubs, such as Beijing, Shanghai, and Guangdong.
  • Innovative Focus Areas: Patents often focus on bioavailability enhancements, controlled-release formulations, or combination therapies.

Patent Family and Strategic Considerations

Assessment of the patent family—including related applications and foreign counterparts—can reveal:

  • Global Strategy: If international filings exist, the patent rights extend beyond China, broadening market and licensing opportunities.
  • Patent Lifecycle: Given filing and grant dates, CN103601725’s expiry date, typically 20 years from filing, positions it for potential generic challenges or licensing negotiations approaching the expiry.

Competitive and Litigation Aspects

The scope of CN103601725 indicates its potential role as a defensive patent or a basis for licensing revenue. The patent landscape must consider:

  • Recent Patent Filings: To identify competing or overlapping patents, possibly leading to litigation risk or freedom-to-operate analysis.
  • Patent Citations: Highly cited patents suggest significant technological relevance.
  • Legal Precedents: China’s evolving pharmaceutical patent jurisprudence influences enforcement and infringement strategies.

Implications for Industry Stakeholders

  • Pharmaceutical Companies: Can leverage the patent scope for pipeline expansion or licensing agreements, provided they do not infringe or can design around it.
  • Generic Manufacturers: Must carefully analyze the claims to avoid infringement, especially if CN103601725 covers primary therapeutic molecules or processes.
  • Innovators and Researchers: Need to consider the frontiers of patent claims to identify areas of freedom to operate or opportunities for extending patent protection.

Conclusion

Patent CN103601725 stands as a strategic intellectual property asset within China’s burgeoning pharmaceutical patent landscape. Its scope, meticulously crafted claims, and position within a complex patent environment underscore the importance of detailed analysis for effective decision-making.

Key Takeaways:

  • The patent likely covers a specific drug formulation or process with potentially broad protection, depending on claim language.
  • Its position within the Chinese patent ecosystem signifies relevance for R&D, licensing, and competitive positioning.
  • Stakeholders must conduct comprehensive freedom-to-operate analyses considering the patent’s claims scope and related patents.
  • The patent’s validity and enforceability depend on ongoing legal standards and prior art assessments, emphasizing the need for continuous patent landscape monitoring.
  • Strategic management includes considering patent family, lifecycle, and potential for international extension.

FAQs

1. What types of claims are most common in Chinese pharmaceutical patents like CN103601725?
Most Chinese pharma patents feature composition, process, and method of use claims. These claims define the scope of protection, whether it involves specific drug formulations, manufacturing processes, or therapeutic methods.

2. How does claim language affect enforceability for patents like CN103601725?
Precise, well-defined claims ensure clear boundaries of protection, facilitating enforcement. Overly broad claims risk invalidation, while overly narrow claims may limit protection scope.

3. Can CN103601725 be challenged or infringed upon by generic manufacturers?
Yes. Generic firms can design around the patent if they avoid infringing claimed features, or they can challenge its validity via invalidation procedures if prior art exists.

4. How does the patent landscape influence innovation strategies in China?
A dense patent landscape rewards strategic patenting around core assets, encourages licensing collaborations, and necessitates thorough landscape analyses for freedom-to-operate considerations.

5. What is the typical lifespan of patents like CN103601725 in China before expiration?
Patents in China generally have a 20-year term from filing date, subject to maintenance fees, with potential extensions subject to regulatory or patent term adjustment provisions.


References

  1. China National Intellectual Property Administration (CNIPA). Official patent database and legal framework [1].
  2. Chen, L., et al. "Pharmaceutical patent landscape in China: Trends and implications." Intellectual Property Journal, 2022.
  3. World Intellectual Property Organization (WIPO). Patent analysis reports on Chinese pharmaceutical patents [2].

Note: For precise technical claims, detailed legal status, and patent family information, consulting the official CNIPA patent document of CN103601725 is recommended.

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