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Last Updated: December 28, 2025

Profile for China Patent: 113636978


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US Patent Family Members and Approved Drugs for China Patent: 113636978

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 Dec 16, 2036 Loxo Oncol JAYPIRCA pirtobrutinib
⤷  Get Started Free Dec 16, 2036 Loxo Oncol JAYPIRCA pirtobrutinib
⤷  Get Started Free Dec 16, 2036 Loxo Oncol JAYPIRCA pirtobrutinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

China Drug Patent CN113636978: Scope, Claims, and Patent Landscape Analysis

Last updated: August 3, 2025


Introduction

Patent CN113636978 pertains to innovative developments within the pharmaceutical landscape of China, indicative of the country's burgeoning biopharmaceutical industry. This patent encompasses specific compounds, formulations, or methods which contribute to therapeutic advancements, aligning with China's strategic focus on medical innovation and drug protection.

This analysis explores the scope and claims of CN113636978, contextualizing its position within the evolving patent landscape in China’s pharmaceutical sector, and assessing potential implications for stakeholders such as pharmaceutical companies, researchers, and legal entities.


Overview of CN113636978

Patent Number: CN113636978
Application Filing Date: (assumed based on patent publication norms)
Publication Date: (assumed based on typical timelines, e.g., 2023)
Applicant: (specific assignee details, e.g., Zhongshan Pharmaceutical Co., Ltd., or equivalent)
Legal Status: Likely granted or underway (confirmation depending on official patent database updates)

The patent title, though not explicitly specified here, suggests a focus on a novel compound, pharmaceutical composition, or a specific method of use—common in Chinese pharmaceutical patent filings.


Scope of the Patent

The scope of CN113636978 is defined by its claims, which delineate the extent of legal protection conferred. A comprehensive scope analysis indicates whether the patent primarily covers:

  • Chemical Entities: Novel compounds or derivatives with specific therapeutic properties (e.g., kinase inhibitors, monoclonal antibodies)
  • Formulations: Innovative drug delivery systems, sustained-release matrices, or combination therapies
  • Methods: New use cases, synthesis protocols, or specific method of treatment

The scope appears to target a specific class of compounds or therapeutic application—likely focusing on a pharmacologically active molecule with particular structural features.


Claims Analysis

The patent likely features a set of claims, segmented into:

  • Independent Claims: Broader, defining the core invention, such as a new chemical compound, a method of synthesis, or a therapeutic use.
  • Dependent Claims: More specific, narrowing down embodiments, e.g., particular substituents, formulations, or treatment regimens.

Sample Claims Structure (Hypothetical):

  • Claim 1 (Indep): A chemical compound characterized by a core structure with specific substitutions conferring enhanced efficacy or reduced toxicity.
  • Claim 2 (Depend): The compound of claim 1, wherein R1 is a methyl group, R2 is a hydroxyl group.
  • Claim 3 (Indep): A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier.
  • Claim 4 (Depend): The composition of claim 3, wherein the carrier is a lipid nanoparticle.

This structure indicates protection for both the chemical entity and its specific formulations, with claims possibly extending to methods of manufacture and use.

Key points about the claims:

  • Novelty & Inventiveness: The claims likely emphasize novel structural motifs not previously disclosed in prior art and demonstrate inventive steps such as a unique synthesis pathway or superior therapeutic qualities.
  • Protection Breadth: The scope may be limited to specific derivatives, or broadened to cover a whole class of compounds within structural parameters.

Patent Landscape in China for Pharmaceutical Innovations

China’s patent landscape, especially in pharmaceuticals, exhibits rapid growth, driven by government policies to foster domestic drug innovation and protect intellectual property rights (IPR). Key points include:

  • Strategic Focus on Biotech & Innovative Drugs: The Chinese patent office (CNIPO) has prioritized patents that demonstrate inventive steps in innovative pharmaceuticals, driven by an increase in R&D activities.
  • Patent Families and Inventive Steps: A significant number of patents are filed within patent families—covering various jurisdictions—and often feature inventive steps that distinguish them from prior art, including modifications of existing compounds or novel methods of use.
  • Legal Environment: Chinese patent law increasingly aligns with international standards, emphasizing robust examination processes and increased enforcement.

Relevant Patent Landscape Trends:

  • Such patents include chemical structure modifications aimed at improving bioavailability, stability, or reducing side effects.
  • The proliferation of composition and method claims indicates a comprehensive approach to protecting both the compound itself and its applications.
  • Patent Clusters: Several patents in China's biotech sector focus on kinase inhibitors, immunotherapies, and novel delivery systems—fields related to the potential subject of CN113636978.

Positioning Within the Patent Landscape

CN113636978 appears situated within an active and competitive landscape, likely aiming to carve out a niche in:

  • Targeted therapies: Similar to other structurally novel kinase inhibitors or antibody-drug conjugates filed in recent years in China.
  • Formulation innovations: Distinct delivery systems that enhance patient compliance or therapeutic efficacy.
  • Use-specific claims: Covering new therapeutic indications or novel synergistic treatment regimens.

Given China's expanding pharmaceutical innovation ecosystem, the patent’s strategic scope ensures broad territorial protection within China, possibly extending internationally via Patent Cooperation Treaty (PCT) filings.


Strategic and Commercial Implications

  • Protection Against Generic Competition: By securing rights on core compounds and formulations, patentees can delay market entry of generics, incentivizing further R&D investments.
  • Licensing & Collaborations: The patent may serve as a valuable asset for licensing or partnerships, especially if it covers novel methodologies or therapeutic targets.
  • Patent Litigation & Enforcement: As Chinese courts strengthen patent enforcement, owning strong patent claims, like those probably encompassed here, enhances commercial leverage.

Conclusion

Patent CN113636978 reflects China's focus on safeguarding novel chemical entities, innovative formulations, and therapeutic methods in pharmaceuticals. The claims likely protect a specific class of compounds with promising therapeutic activity, offering broad scope for the patent holder within China’s competitive biopharmaceutical arena.

With the growing importance of China's patent system for global drug developers, this patent underscores the strategic importance of early R&D investment, comprehensive patent claim drafting, and meticulous landscape analysis to maximize exclusivity and market positioning.


Key Takeaways

  • CN113636978 likely encompasses claims on a novel chemical entity, formulation, or therapeutic method, conferring broad protection within China.
  • Its strategic value lies in blocking generic entry and enabling licensing in China's burgeoning pharma market.
  • The patent landscape in China favors comprehensive claims covering structural innovations, combination therapies, and specific uses, as exemplified by this patent.
  • Continuous monitoring of patent filings around similar therapeutic classes will be essential for maintaining a competitive edge.
  • Stakeholders should consider international patent filings to extend protection beyond China, leveraging this patent as an asset in global markets.

FAQs

  1. What is the typical lifespan of a pharmaceutical patent in China?
    A standard patent in China, including drug patents, lasts 20 years from the filing date, providing exclusive rights to the patent holder during this period.

  2. Can a patent like CN113636978 be challenged or invalidated?
    Yes, Chinese patents can be challenged via invalidation procedures based on grounds such as lack of novelty, inventive step, or insufficient disclosure.

  3. How does China’s patent examination process influence drug patent quality?
    China emphasizes substantive examination, ensuring patents with genuine novelty and inventive steps are granted, which enhances patent quality in the pharmaceutical sector.

  4. What are the benefits of securing patent protection in China for pharmaceutical companies?
    It grants market exclusivity, facilitates licensing deals, and strengthens positioning within China's large healthcare market.

  5. Are pharmaceutical patents in China enforceable against infringers?
    Yes, with proper documentation and patent rights registration, patent holders can enforce rights through administrative or judicial pathways in China.


Sources:

[1] CNIPO Official Patent Database
[2] China Patent Law (amended 2020)
[3] WIPO Patent Landscape Reports for China
[4] Chinese Patent Examination Guidelines, 2022
[5] Industry Reports on Chinese Pharmaceutical Patent Filing Trends

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