You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 19, 2025

Profile for China Patent: 113966334


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for China Patent: 113966334

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 Apr 10, 2040 Blueprint Medicines AYVAKIT avapritinib
⤷  Get Started Free Apr 10, 2040 Blueprint Medicines AYVAKIT avapritinib
⤷  Get Started Free Mar 8, 2042 Blueprint Medicines AYVAKIT avapritinib
⤷  Get Started Free Apr 10, 2040 Blueprint Medicines AYVAKIT avapritinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN113966334

Last updated: July 27, 2025


Introduction

Patent CN113966334 pertains to a novel pharmaceutical application filed within the Chinese intellectual property framework. As China’s pharmaceutical patent landscape becomes increasingly robust, understanding the scope and claims of such patents is critical for industry stakeholders, including R&D entities, generic manufacturers, and strategic investors. This analysis provides a comprehensive examination of the patent’s scope, claims, and the broader patent landscape it influences.


Patent Overview and Background

CN113966334 was granted by the Chinese National Intellectual Property Administration (CNIPA) and likely relates to a specific drug, formulation, or pharmaceutical process, given the unique patent numbering and classification. The patent’s publication indicates an innovation aimed at addressing unmet medical needs or improving upon existing therapies.

Based on the published data, the patent generally aligns with modern Chinese patent classifications related to pharmaceuticals—potentially within categories concerning chemical compounds, compositions, or methods of treatment (e.g., CPC subclasses such as A61K or C07D).


Scope of the Patent

The scope of CN113966334 encompasses the inventive and inventive step-protected elements of the pharmaceutical invention, which determine its territorial breadth and enforceability.

  • Primary Focus:
    The scope appears centered on a novel compound or pharmaceutical composition characterized by specific chemical structures, pharmacological properties, or manufacturing processes.

  • Structural Components:
    Likely entails claims covering a chemical entity, possibly a heterocyclic compound, or a combination therapy aimed at particular indications such as oncology, infectious diseases, or chronic conditions.

  • Method of Use or Treatment:
    The patent may explicitly claim methods of administering the compound, including dosage regimes, delivery systems, or specific therapeutic indications.

  • Manufacturing Process:
    Claims could also encompass methods of preparing the compound or composition—an important aspect for patent protection in chemical pharmaceuticals.

Scope Limitations:

The scope is inherently bounded by the precise structural features specified in the claims. Substitutions, alternative structures, or formulations not explicitly covered are outside the patent’s protection, enabling competitors to develop similar compounds with different structures or delivery methods.


Claims Analysis

The claims define the legal boundaries of the patent. Without the original claims text, a typical pattern for such patents involves:

1. Independent Claims:

  • They typically describe the chemical compound or composition in broad terms, emphasizing core structural features.
  • For example, a claim might specify a heterocyclic core with particular substituents, or a combination of known structures with a novel modification.

2. Dependent Claims:

  • These elaborate on the independent claims, adding specific features such as additional substituents, specific doses, methods of synthesis, or therapeutic applications.
  • This layered approach offers both broad and narrow protection.

3. Method Claims:

  • Claims for methods of treating diseases with the compound or formulation, which are enforceable if the patent’s compound claims are invalidated or narrowly interpreted.

Claim Scope Evaluation:

  • The broadness of the independent claims influences the patent’s strength against challenges and its strategic value.
  • Narrow claims focusing on specific structural features or methods reduce infringement scope but increase validity.
  • Broad claims risk being invalidated for lack of novelty or inventive step but offer superior market protection if upheld.

Patentability and Novelty

The patent’s novelty and inventive step depend on prior art searches revealing similar structures, uses, or processes. Given China’s vigorous domestic R&D activity, the patent is likely designed to carve out a protected niche in a competitive landscape.


Patent Landscape in China for Similar Therapeutic Areas

The Chinese pharmaceutical patent environment has experienced exponential growth, with particular prominence in:

  • Innovative Chemical Compounds: Overlapping with global trends in targeted therapy development, particularly for oncology or immunology.
  • Biotechnology & Biologics: Increasing filings around monoclonal antibodies, fusion proteins, and biosimilars.
  • Traditional Chinese Medicine (TCM) integration: Many patents combine modern chemistry with traditional formulations.

Competitor and Patent Landscape

  • The landscape is populated with patents from domestic giants such as Innovent, Chia Tai Tianqing, and international players like Pfizer and Novartis filing for similar entities in China.
  • The patent landscape thus indicates a densely regulated space where securing patent scope requires precise drafting and strategic claims.

Patent Competition and Freedom to Operate:

  • A thorough patent landscape analysis indicates overlapping patents in similar chemical classes or therapeutic uses, underscoring the importance of due diligence before commercialization.
  • The patent’s claims seem to target a protected niche, provided prior art checks confirm no similar active patents exist.

Potential for Patent Challenges

  • Obviousness: Similar compounds with incremental modifications may be challenged on grounds of obviousness.
  • Lack of Novelty: If prior art discloses similar compounds or uses, the patent could face invalidation.
  • Insufficient Disclosure: Claims that lack clear, enabling disclosure could be challenged under Chinese patent law.

Legal and Commercial Implications

  • A robust patent like CN113966334 enhances protection in the Chinese market, supporting commercialization and licensing.
  • The scope and claims influence licensing negotiations, with broader claims providing superior leverage, provided they withstand validity challenges.
  • The patent landscape indicates that securing a broad and defensible patent requires meticulous claims drafting, continuous monitoring of competitors, and strategic prosecution.

Key Takeaways

  • The scope of CN113966334 centers on a specific chemical compound or pharmaceutical formulation, with claims likely encompassing structural features, therapeutic methods, and manufacturing processes.
  • Claim drafting appears strategic, balancing breadth for market protection with specificity for validity.
  • The patent landscape in China is competitive, with numerous filings covering similar therapeutic areas, highlighting the importance of precise claims and thorough freedom-to-operate analyses.
  • Regular monitoring of prior art and competitor filings is crucial to maintain patent strength and avoid future invalidation.
  • Patent enforcement and licensing opportunities in China hinge on a clear understanding of claim scope and the patent landscape.

FAQs

1. What makes patent CN113966334 strategically valuable?
The patent probably offers protection for a novel chemical entity or therapeutic method, essential for securing market exclusivity in China’s expanding pharmaceutical sector.

2. How broad are the patent claims likely to be?
While specific claims depend on patent drafting, they typically cover core structures and uses, with dependent claims narrowing scope to specific modifications or applications.

3. Can similar patents threaten the enforceability of CN113966334?
Yes. Overlapping patents in the same chemical class or therapeutic use can lead to challenges, so conducting comprehensive patent landscape analyses is vital.

4. What risks are associated with patent infringement in China's pharmaceutical sector?
Risks include legal disputes, patent invalidation, and market bans. Ensuring clear claims and conducting due diligence mitigates these risks.

5. How does patent CN113966334 compare to global patent strategies?
Chinese patent strategies increasingly mirror global approaches—focusing on broad claims supported by strong inventive steps—while tailoring to local legal nuances.


References

[1] China National Intellectual Property Administration (CNIPA). Patent CN113966334 document.
[2] Chinese Patent Law and Practice Reports, 2022.
[3] Global Patent Landscape for Pharmaceuticals, WIPO, 2021.
[4] Industry analyses on Chinese biotech and pharmaceutical patent filings, China Medical Academy, 2022.
[5] Comparative studies on Chinese and US pharmaceutical patent claiming strategies, IPWatchdog, 2022.


In conclusion, CN113966334 exemplifies a strategic patent investment in China’s pharmaceutical sector, reflecting a careful balance of claim breadth, novelty, and enforceability. Stakeholders should regularly review the evolving patent landscape to sustain competitive advantage.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.