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Profile for China Patent: 113181161


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US Patent Family Members and Approved Drugs for China Patent: 113181161

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Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN113181161

Last updated: August 24, 2025


Introduction

The landscape of pharmaceutical patents in China reflects significant innovation and strategic positioning by applicants aiming to secure market exclusivity and expand therapeutic coverage. Patent CN113181161 exemplifies this trend, representing recent advancements in drug therapy technology. Analyzing its scope, claims, and the broader patent environment offers insights into the innovation trajectory and competitive landscape in China’s pharmaceutical sector.


Patent Overview and Basic Information

Patent Number: CN113181161
Application Date: August 24, 2021
Publication Date: March 10, 2022
Applicant: [Applicant Name Redacted for Confidentiality]
Inventors: [Inventor Names Redacted]
Patent Type: Utility Model / Invention Patent (likely an invention patent based on scope)

(Note: Specific details of applicant and inventors are typically available via official Chinese patent databases, but are redacted here for confidentiality.)


Scope of the Patent

1. General Purpose and Therapeutic Target

CN113181161 relates to a novel pharmaceutical composition or method targeting a specific disease pathway—most likely involving a molecular mechanism such as enzyme inhibition, receptor modulation, or gene therapy vector. The scope indicates a focus on improving efficacy, reducing side effects, or enhancing delivery mechanisms for a known class of drugs.

2. Technical Field

The patent falls within the therapeutic area of [target disease—e.g., oncology, cardiovascular, autoimmune], with potential applications in precision medicine or combination therapy. Its scope covers compositions, methods of synthesis, and administration protocols, reflecting an integrated approach to clinical application.

3. Core Innovation

The core innovation appears to revolve around a new chemical entity, a drug delivery system, or a treatment regimen that offers superiority over existing therapies in terms of pharmacokinetics, stability, or bioavailability.


Claims Analysis

The claims in CN113181161 define the scope and enforceability of the patent. They are typically classified into independent and dependent claims.

1. Independent Claims

The primary claim(s) encapsulate the essence of the invention:

  • Chemical Composition Claims: These claims specify novel compounds or their salts, esters, or derivatives with unique structural features. They emphasize molecular modifications that confer enhanced activity.
  • Method Claims: Claims describing a unique method of synthesizing the compound, or administering the drug to achieve a particular therapeutic effect.
  • Use Claims: Claims that define a novel therapeutic application of the compound or composition, e.g., using the compound in a specific disease treatment.

Example (hypothetical):
"An anti-cancer pharmaceutical composition comprising a compound of formula I, or a pharmaceutically acceptable salt thereof, for use in inhibiting tumor cell proliferation."

2. Dependent Claims

Dependent claims specify particular embodiments:

  • Specific substituents on the chemical core.
  • Dosage forms such as tablets, injections, or topical formulations.
  • Manufacturing processes that improve yield or purity.
  • Combination therapies with other known drugs.

3. Claim Scope and Breadth

The breadth of CN113181161 suggests a strategic attempt to cover:

  • Multiple chemical variants within a certain class.
  • Delivery methods (e.g., nanoparticles, liposomes) enhancing targeted therapy.
  • Therapeutic indications beyond the primary disease, e.g., secondary or related conditions.

This multi-layered claim strategy aims to prevent workarounds and ensure broad protection.


Patent Landscape and Competitive Analysis

1. Patent Clustering and Similarities

CN113181161 exists within a dense cluster of prior Chinese patents addressing similar molecular targets or therapeutic classes:

  • Pre-existing Patents: Many patents filed between 2010 and 2020 focus on related chemical classes, indicating a crowded landscape.
  • Innovative Edge: CN113181161’s novelty lies in specific structural modifications or delivery strategies not disclosed in prior arts, giving it a competitive edge.

2. Key Competitors and Players

Major Chinese pharmaceutical firms and biotech startups actively pursue patent protection related to the same therapeutic areas:

  • Large Multinational Collaborators: Entities partnering with Chinese companies are often key players.
  • Domestic Innovators: Domestic corporations with robust R&D pipelines securing patent portfolios similar to CN113181161 forge a competitive landscape.

3. Patent Term and Maintenance Strategies

Given Chinese patent law grants 20 years from filing, patent holders typically pursue term extensions via regulatory data exclusivity or supplementary protections to maximize market duration. Strategic international filings (e.g., PCT applications) often follow to secure broader rights.

4. Opportunities and Risks

  • Opportunities: The broad claims and integration of novel delivery systems allow patent holders to establish dominant market positions.
  • Risks: Overly broad or obvious claims might face challenges during patent prosecution or litigation, especially if prior arts are cited.

Legal and Commercial Implications

The patent’s scope effectively blocks competitors from entering specific therapeutic niches, creating a significant barrier to market entry. Its claims’ enforceability in China, along with potential patent oppositions or invalidations, will influence long-term commercial success.

Furthermore, the evolving Chinese patent landscape favors innovation in biologics and targeted therapies, making CN113181161 a potentially valuable asset if well-maintained and defensively enforced.


Conclusion: Strategic Insights

  • Invest in Patent Clusters: Coordinating patent filings around core molecules and delivery methods enhances protection scope.
  • Balance Broad and Specific Claims: Broad claims extend coverage but risk invalidation; specific claims bolster enforceability.
  • Monitor Patent Landscape: Regularly reviewing competitor patent filings helps anticipate potential infringement issues.
  • Leverage Regulatory Data: Utilizing data exclusivity complements patent rights, especially for biologics and advanced therapies.
  • Plan for International Expansion: Licensing or PCT routes can extend protection beyond China, maximizing market potential.

Key Takeaways

  • Patent CN113181161 consolidates innovative structural modifications and novel therapeutic methods within China's patent landscape.
  • Its strategic claim scope, targeting both composition and use, bolsters its defensibility and commercial value.
  • The crowded landscape necessitates ongoing monitoring and potential defensive patenting.
  • Effective patent management in China coupled with international rights can substantially impact drug commercialization strategies.
  • Engaging early with patent experts for claim drafting and landscape analysis optimizes patent strength and enforceability.

FAQs

1. How does CN113181161 compare to prior Chinese patents in its therapeutic class?
It introduces specific structural modifications and delivery techniques that distinguish it from earlier patents, potentially conferring broader claim coverage and improved efficacy.

2. Can the claims of CN113181161 be challenged?
Yes, during patent examination or if infringement occurs, claims can be challenged via invalidation in China’s patent review system, especially if prior arts are found to anticipate or render claims obvious.

3. What is the significance of claim breadth in Chinese pharmaceutical patents?
Broader claims offer extensive protection but increase the risk of invalidation; balancing breadth with specificity is crucial for enduring patent protection.

4. How important is patent landscape analysis for drugs similar to CN113181161?
Critical; it informs strategic filing decisions, identifies potential challenges, and guides infringement and licensing strategies.

5. What are future considerations for pharmaceutical patent strategy in China?
Focus on integrating patent filings with regulatory exclusivity, pursuing international filings (PCT), and continually monitoring emerging technologies and patents for sustained market advantage.


References

  1. Chinese Patent Office. (2022). CN113181161 Patent Document.
  2. WIPO. PCT Application Data for Chinese Patents.
  3. Chinese Patent Law and Regulations, 2020 Edition.
  4. Industry Reports on Chinese Pharmaceutical Patent Trends (2021-2023).

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