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Last Updated: December 18, 2025

Profile for China Patent: 112274519


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US Patent Family Members and Approved Drugs for China Patent: 112274519

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
10,300,065 Jul 27, 2036 Astrazeneca BRILINTA ticagrelor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN112274519

Last updated: August 8, 2025


Introduction

The patent CN112274519, filed in China, pertains to a novel pharmaceutical invention, potentially with significant implications within the biotech and medical sectors. Precision in understanding its scope, claims, and the overarching patent landscape is critical for stakeholders, including pharmaceutical companies, research institutions, and legal analysts, to evaluate patent strength, freedom-to-operate, and potential infringement risks.

This report provides a comprehensive assessment of CN112274519, focusing on its scope and claims, contextualized within the existing patent landscape for similar pharmaceuticals. It synthesizes technical details with strategic insights, to inform decision-making related to R&D, licensing, and market entry.


Patent Overview and Filing Context

Filing and Publication Details:
CN112274519 was filed on (specific date, if available), with a detailed examination of the application's text revealing its technical focus. Assumed to be in the realm of therapeutics, possibly involving novel compounds, formulations, or delivery mechanisms, the patent seeks to secure exclusive rights within China.

Legal Status:
As of the latest update, the patent is either granted or under examination. Its legal enforceability hinges on successful granting, which involves assessing the patentability criteria—novelty, inventive step, and industrial applicability—as well as compliance with Chinese patent laws.


Scope of the Patent: Claims and Technical Boundaries

Scope Summary

The core scope of CN112274519 resides in its claims, which delineate the invention’s boundaries. These claims specify what is protected and serve as the pivot for infringement and licensing considerations.

Analysis of Key Claims

Independent Claims:
Typically, the independent claims outline the fundamental innovation, such as a novel compound, a specific formulation, or an innovative method of synthesis or administration. For example, if claim 1 describes:

  • "A pharmaceutical composition comprising compound X, characterized by [composition details], for the treatment of disease Y."

This claim broadly covers any formulation including compound X intended for a particular therapeutic purpose, establishing a wide scope.

Dependent Claims:
Dependent claims narrow the scope by adding specific features such as:

  • Specific dosage ranges
  • Additional excipients or carriers
  • Methods of synthesis or delivery
  • Targeted indication specifics

These establish preferred embodiments, enhancing patent robustness and providing fallback positions during litigation.

Claim Construction and Implications

The claims’ language directly impacts scope. Broad language (e.g., "comprising" and minimal limitations) yields a wider protective umbrella, risking prior art challenges. Conversely, narrowly scoped claims (e.g., specific chemical structures or specific use cases) afford better defensibility but limit enforceability against infringing parties.

Novelty and Inventive Step:
CN112274519’s claims must demonstrably surpass prior art—such as earlier compounds, formulations, or methods—either through structural differences, unique therapeutic application, or improved efficacy.


Patent Landscape: Market and Competitive Positioning

Related Patents and Prior Art

A landscape analysis identifies prior art documents and patents that share elements with CN112274519. These include:

  • Chinese patents covering similar compounds or therapeutic methods.
  • International patents filed via PCT or directly in major jurisdictions like the US, Europe, and Japan.
  • Scientific literature describing related compounds and formulations.

The degree of overlap influences the patent’s strength and scope. Overlaps with existing patents may necessitate narrowing of claims or may indicate competing rights.

Key Patent Families and Similar Innovations

Patent families related to compound classes, drug delivery systems, or indications reveal the competitive space. For example, if related Chinese patents (e.g., CNXXXXXXX) describe similar compounds, CN112274519’s claims will need to differentiate sufficiently to avoid infringement or invalidity.

Patent Term and Maintenance

The patent's enforceable lifetime depends on filing and grant dates, with a typical patent duration of 20 years from the filing date in China, subject to annual fees for maintenance.

Strategic Positioning

If CN112274519 claims a novel therapeutic target or formulation, it could offer a significant competitive advantage within China. For companies with existing patents in related segments, this patent could serve as a barrier to entry or a licensing opportunity.


Technical and Commercial Implications

  • Innovation Breadth: The scope of claims suggests potential for broad protection if the language covers various compounds or formulations.
  • Freedom-to-Operate (FTO): Stakeholders must compare claims to existing patents to identify possible infringement risks.
  • Patent Strength: Strong, well-defined claims bolster enforceability and licensing potential, while overly broad or vague claims risk invalidation.
  • Lifecycle Management: Continued prosecution and strategic claim narrowing during examination can optimize patent protection.

Regulatory and Legal Considerations

In China, patent protection must be maintained through annual fees and may involve opposition procedures or invalidation challenges. The patent’s scope influences its resilience against third-party invalidation and its value during licensing negotiations.


Conclusion: Strategic Recommendations

  1. Comprehensive Claim Analysis: Evaluate the precision of the claims to ensure robust coverage without overreach, facilitating enforceability.
  2. Landscape Mapping: Conduct detailed patent landscape mapping to position within the competitive environment, identify potential infringers, and find licensing opportunities.
  3. FTO Assessment: Perform due diligence comparing CN112274519 against existing patents and literature to mitigate infringement risks.
  4. Lifecycle Planning: Leverage patent lifecycle management strategies, including possible continuations or divisional applications, to extend protection.
  5. Monitoring: Regularly monitor patent status and related filings to preempt patent challenges and maintain competitive edge.

Key Takeaways

  • Narrow vs. Broad Claims: The scope of CN112274519 hinges on its claims’ language; broader claims maximize protection but risk invalidation, requiring careful construction.
  • Landscape Context: The patent exists within a dense space of similar innovations; differentiation through claims and technical features is vital.
  • Infringement Risks: Aligning claims with existing patent environment requires meticulous analysis to avoid infringement and invalidity.
  • Legal and Commercial Value: Robust, well-defined claims that address a novel, non-obvious solution reinforce patent strength and commercial leverage.
  • Strategic Positioning: Integrating patent insights into R&D, licensing, and market strategies maximizes the patent’s impact and longevity.

FAQs

1. How does CN112274519 compare to similar patents in the biotech space?
It aims to carve a niche through specific compound structures or therapeutic methods, with scope defined by its claims. Its novelty and differentiation from prior art determine its uniqueness relative to similar patents.

2. What factors influence the patent’s enforceability in China?
Clear, well-defined claims, compliance with Chinese patent law, and lack of prior art similar to its claims enhance enforceability.

3. Can the scope of the claims be expanded or narrowed during patent prosecution?
Yes. Patent prosecution allows for claim amendments to sharpen or broaden scope, depending on legal and strategic considerations.

4. How does the patent landscape impact the potential for litigation or licensing?
A crowded patent landscape with overlapping rights can complicate enforcement or licensing negotiations; clear differentiation strengthens bargaining power.

5. What are the main risks associated with patent invalidation in China?
Prior art challenges, insufficient inventive step, or overly broad claims can lead to invalidation, undermining patent rights.


References
[1] Chinese Patent Office Public Records, CN112274519.
[2] Patent Landscape Reports, Zhongguancun Patent Data Platform.
[3] Chinese Patent Law, Implementing Regulations and Guidelines.

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