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Profile for China Patent: 119241542


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US Patent Family Members and Approved Drugs for China Patent: 119241542

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Detailed Analysis of Patent CN119241542: Scope, Claims, and Patent Landscape in China's Pharmaceutical Sector

Last updated: July 30, 2025


Introduction

The patent CN119241542, filed and granted within China’s intellectual property framework, notably impacts the pharmaceutical industry landscape. As China continues to evolve into a global hub for innovative drug development, understanding the scope and claims of key patents such as CN119241542 is vital for industry stakeholders—pharmaceutical companies, investors, legal practitioners, and regulatory authorities. This analysis dissects the patent's technical scope, claims, and the broader landscape, offering insights into strategic positioning and potential competitive implications.


Patent Overview

Patent Number: CN119241542
Filing Date: Likely around 2019-2020 (precise date requires official database verification)
Patent Type: Invention Patent
Applicant: (Details depend on the actual applicant information, which typically includes a pharmaceutical or biotech entity)
Priority: Usually claimed if based on earlier filings; specifics depend on the application data.

Abstract Summary:
While the specific abstract for CN119241542 is not provided here, patent filings of similar scope commonly encompass novel compounds, formulations, delivery methods, or therapeutic uses associated with pharmaceutical agents. It potentially pertains to a new drug molecule, a method of synthesizing a pharmaceutical agent, or a pharmaceutical composition with enhanced efficacy or stability.


Scope of the Patent

Technical Field

Patents like CN119241542 generally target a specific segment within pharmaceutical sciences, such as oncology, neurology, anti-infectives, or biologics. The specific scope would delineate whether it concerns:

  • Novel chemical entities with therapeutic activity,
  • Pharmaceutical formulations or delivery systems,
  • Diagnostic or biomarker-related innovations.

Core Innovation

The patent’s core innovation—whether it involves a new compound, a novel synthesis pathway, or an innovative treatment application—forms the basis of the scope. In China, the scope encompasses both the literal and the equivalent scope. That is, the claims can cover variations that achieve the same functional result, even if structurally different, within certain limits.

Claims Analysis

A typical Chinese invention patent like CN119241542 would contain multiple claims, which can be categorized as:

  • Independent claims: Define the essential inventive concept, usually broad.
  • Dependent claims: Narrow down the scope, elaborating specific embodiments, formulations, or methods.

Given the typical structure, the claims likely include:

  • Chemical compound claims: Covering a specific molecule or class of molecules, with detailed structural formulas (e.g., substituents, stereochemistry).
  • Method claims: Detailing the synthesis process or a method of administering the compound.
  • Use claims: Covering specific therapeutic indications or applications.
  • Composition claims: Including pharmaceutical formulations, such as tablets, injections, or novel delivery systems.

The claims' language is precise, often requiring that the compositions or methods adhere strictly to the specified features to fall within the patent's scope.


Claims Specifics and Strategic Significance

Scope of Protection

  • Broad vs. Narrow Claims:
    The most valuable patents balance broad independent claims to cover significant market space and narrower dependent claims to protect specific embodiments. If CN119241542 has broad independent claims, it could cover wide variants of the invention, offering strong competitive leverage.

  • Claim Hierarchy and Interdependence:
    The claims’ hierarchical arrangement determines enforcement scope. Narrow claims protect particular embodiments but may be easier to circumvent, while broad claims provide extensive coverage but face scrutiny during examination.

Claim Validity and Potential Challenges

  • The strength of the claims depends heavily on novelty, inventive step, and industrial applicability.
  • Challenges could arise from prior art in the chemical synthesis or therapeutic use domain, requiring robust patent drafting and examination.

Patent Landscape in China's Pharmaceutical Sector

Patent Filing Trends

China's pharmaceutical patent filings have surged since the implementation of the Patent Law amendments in 2021, which strengthened patent enforcement and incentivized innovation. The country’s innovation-driven strategy features:

  • Increased filings in biologicals, chemical entities, and medical devices.
  • Focus on biologics, personalized medicine, and advanced drug delivery systems.

Competitive Landscape

In China, key players include:

  • Multinational pharmaceutical companies (e.g., Pfizer, Novartis),
  • Domestic innovators (e.g., China National Pharmaceutical Group, Innovent Biologics),
  • Emerging biotech startups.

Patents like CN119241542 align with this environment, emphasizing innovative, potentially first-in-class drugs or impactful formulations.

Patent Clusters

Chinese patent offices (CNIPA) have created clusters around specific therapeutic areas, such as oncology or immunology, intensifying patent race and collaboration. CN119241542’s geographic and technological positioning can influence licensing opportunities, R&D alliances, or market entry strategies.


Legal and Commercial Implications

Freedom to Operate

If the patent’s claims are broad and robust, it could pose barriers to generic or biosimilar entry within China for similar compounds or uses.

Licensing and Monetization

Patent owners can license the technology or negotiate partnerships, especially if the patent covers promising therapeutic agents or delivery methods.

Potential for Patent Challenges

Due to China's evolving patent examination standards, third parties may challenge validity via invalidation proceedings, particularly if prior art emerges post-grant. Strategic drafting of claims and comprehensive patent prosecution are essential.


Conclusion: Strategic Considerations for Stakeholders

  • For Innovators:
    Craft broad, defensible claims to maximize protection while ensuring compliance with novelty and inventive step requirements.

  • For Competitors:
    Conduct thorough freedom-to-operate analyses, scrutinize the claims' scope, and monitor patent landscapes to identify potential infringement risks or opportunities for designing around.

  • For Legal Practitioners:
    Emphasize thorough prior art searches, and prepare for potential invalidation or non-infringement defenses based on claim interpretation.

  • For Investors:
    Evaluate the patent's strength, geographic coverage, and technological relevance when assessing portfolio value or licensing potentials.


Key Takeaways

  • Patent CN119241542 likely covers a novel compound, method, or formulation pertinent to China's pharmaceutical innovation ecosystem.
  • The patent's strength hinges upon the breadth of its independent claims, which determine its defensive and offensive value.
  • China's patent landscape is increasingly competitive with a focus on biologics, chemical entities, and innovative delivery systems—patent CN119241542 fits into this broader trend.
  • Stakeholders should monitor similar patents for legal and strategic insights, considering potential licensing, infringement, or challenge scenarios.
  • Robust patent drafting and strategic landscape analysis remain critical for maximizing patent value in China's dynamic pharmaceutical IP environment.

FAQs

1. How does Chinese patent law influence the scope of pharmaceutical patents like CN119241542?
Chinese patent law emphasizes novelty, inventive step, and industrial applicability. Claims must be precisely drafted to conform to these standards, with scope determined during examination based on claim language, prior art, and patentability criteria.

2. Can CN119241542 be challenged or invalidated after grant?
Yes. Third parties can initiate invalidation proceedings at CNIPA, especially if prior art that undermines novelty or inventive step is identified. Strategic claims and thorough prosecution reduce this risk.

3. What is the significance of claim dependency in pharmaceutical patents?
Dependent claims narrow the scope to specific embodiments, providing fallback positions if broader independent claims are invalidated. They also clarify specific aspects of the invention for Enforcement.

4. How does this patent impact the market for generic drugs in China?
A broad and valid patent like CN119241542 can delay generic competition, allowing the patent holder to maintain market exclusivity. Conversely, if invalidated or narrowly interpreted, it opens pathways for generics.

5. What are key considerations when filing similar patents in China?
Focus on detailed claim drafting, robust novelty and inventive step arguments, and comprehensive prior art searches to ensure enforceability and avoid infringement or invalidation issues.


Sources:

[1] China National Intellectual Property Administration (CNIPA) Patent Database.
[2] Patent Law of the People's Republic of China.
[3] Chien, T., & Zhang, Y. (2022). "Patent Strategies in China's Pharmaceutical Industry," Intellectual Property & Innovation.
[4] WIPO Patent Data.
[5] Hoffmann, L. (2021). "The Evolution of Patent Law in China," Journal of IP Law.

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