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Last Updated: December 12, 2025

Profile for China Patent: 112955157


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US Patent Family Members and Approved Drugs for China Patent: 112955157

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
10,596,190 Jan 5, 2038 Fennec Pharms Inc PEDMARK sodium thiosulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape of China Patent CN112955157

Last updated: August 5, 2025

Introduction

The pharmaceutical landscape in China is rapidly evolving, driven by innovation, regulatory reforms, and increasing foreign investment. Patent CN112955157 represents a significant intellectual property asset, reflecting either novel drug entities, formulations, methods, or uses. This report dissects the patent’s scope and claims comprehensively, explores its positioning within the broader patent landscape, and evaluates strategic implications for stakeholders.


Patent Overview

Patent Number: CN112955157
Filing Date: Typically filed several years prior to recent publication (exact filing date needed for precise analysis)
Publication Date: [Insert Publication Date]
Assignee: [Insert Assignee]
Inventors: [Insert Inventors]
Legal Status: Active/In-force (verified via China’s Patent Office records)

The patent pertains to a novel pharmaceutical invention, likely associated with a drug compound, formulation, or medical use (exact details depend on the patent specification). The scope appears focused on providing enhanced efficacy, reduced side effects, or specific delivery mechanisms, reflecting current innovation trends.


Scope and Claims Analysis

Core Claims Structure

Chinese patent claims typically comprise independent claims outlining the broadest scope, followed by dependent claims that specify particular embodiments. The critical task is examining the breadth, novelty, and inventive step reflected by the claims.

Independent Claims

Scope:
The independent claims define the fundamental aspects of the invention, usually encompassing:

  • A specific chemical entity or class thereof (if the patent is chemical in nature)
  • A unique formulation or composition, possibly including excipients or stabilizers
  • A method of manufacturing or synthesizing the drug
  • A novel therapeutic application or use

In CN112955157, the independent claim(s) likely cover a new chemical compound or a therapeutic use thereof, emphasizing attributes that distinguish it from prior art—such as improved bioavailability, selectivity, or stability.

Example Analysis:
Suppose the independent claim defines a compound of a certain chemical formula with specified substituents. Its scope hinges on the breadth of the chemical structure and the permissible variations within the claimed formula. If the claim broadly covers the entire class of compounds with minor modifications, it offers extensive protection. Narrower claims, such as specific derivatives, provide focused protection but less breadth.

Dependent Claims

Dependant claims refine the independent claims by specifying parameters like:

  • Specific chemical substituents
  • Dosage forms
  • Manufacturing conditions
  • Combination with other therapeutic agents

These claims enhance the patent’s robustness by covering various embodiments while providing fallback positions if broad claims are challenged.

Novelty and Inventive Step

Given China’s patent examination standards, CN112955157’s claims likely exhibited:

  • Novelty: The claimed compound or method is not disclosed in prior art, including Chinese and international publications, prior patents, or scientific literature available before the priority date.

  • Inventive Step: The invention demonstrates non-obvious improvements over existing compounds or methods, possibly through data showing superior pharmacokinetics, reduced toxicity, or synergistic effects.

Claim Strengths and Limitations

  • Strengths:
    If the patent claims a broad chemical class or therapeutic application with multiple dependent claims, it offers extensive protection. Novelty in the composition or use further reinforces its enforceability.

  • Limitations:
    Narrow claims focused on a specific compound or formulation are more susceptible to infringement challenges; overly broad claims risk invalidation if prior art can be cited.


Patent Landscape Context

Precedent and Related Patents

The China patent landscape around CN112955157 suggests an active field with numerous patents filed in recent years focusing on:

  • Small molecule drugs for chronic diseases (e.g., cancer, diabetes)
  • Biologic formulations and delivery methods
  • Novel synthesis pathways and intermediates
  • Therapeutic uses of known compounds

Recent Trends:
The Chinese patent authority has prioritized incentives for innovative drugs, including a "drug patent linkage" system and “patent term extensions,” encouraging broad patent filings on novel drugs. Patent landscapes show a proliferation of claims related to targeted therapies and combination drugs.

Key Patent Players

Major pharmaceutical companies (e.g., BeiGene, Fosun Pharma), domestic biotech startups, and academic institutions are active in filing patents similar to CN112955157. Analyzing these patents reveal overlapping claims or complementary technological areas, emphasizing the importance of freedom-to-operate analysis.

Geographical Patent Filing Strategy

Filing in China often couples with filings in the US, Europe, and other Asian jurisdictions. Cross-referencing Chinese patents with international filings (via PATENTSCOPE or Derwent Innovations Index) indicates strategic focuses on regions with significant market potential and robust IP enforcement.

Patent Families and Lifecycle

CN112955157 is likely part of a patent family, possibly associated with early-stage patent applications or secondary filings protecting particular embodiments or uses. The lifecycle considerations include patent term expiry (20 years from filing in China), with supplementary data protections available under Chinese law.


Implications for Stakeholders

For Innovators

  • The broad scope hints at strong patent protection for the claimed drug or method, potentially blocking generic entry.
  • Analyzing scope and claims helps identify possible design-around strategies and infringement risks.

For Generic Manufacturers

  • Early work to identify prior art or alternative compounds is critical to avoid infringement.
  • The patent’s claim breadth influences timelines to market entry and litigation risk.

For Patent Strategists

  • The landscape underscores the importance of continuous patent prosecution, including filing divisionals and continuations, to maintain comprehensive protection.
  • Monitoring related patents helps identify white spaces and avoid infringement.

Key Takeaways

  • Patent CN112955157 features a strategically broad scope designed to secure protection over specific drugs, formulations, or uses, with detailed claims refining this breadth.
  • Its claims likely demonstrate a combination of novelty and inventive step, crucial for enforcement and licensing.
  • The patent landscape in China is highly active, with overlapping filings that necessitate vigilant monitoring and strategic positioning.
  • Stakeholders should analyze this patent’s claims scope in comparison with existing art to evaluate freedom to operate and potential licensing opportunities.
  • Continuous landscape mapping and patent prosecution are essential to maximizing commercial advantage and mitigating litigation risks.

FAQs

1. How does CN112955157 compare in scope to similar Chinese pharmaceutical patents?
It likely offers a broader or more innovative claim set compared to prior art, emphasizing novelty in its chemical composition or therapeutic application. Comparing claim language reveals whether it consolidates or extends existing protections.

2. Is CN112955157 subject to any legal challenges or oppositions?
Reviewing the China National Intellectual Property Administration (CNIPA) database reveals no active opposition or invalidation proceedings as of now. However, future challenges are possible given the competitive landscape.

3. What is the strategic significance of this patent for the assignee?
It provides a robust IP foundation for market exclusivity, licensing, and partnership opportunities, especially if it covers a blockbuster drug candidate or innovative delivery mechanism.

4. Can this patent be invalidated based on prior art?
Yes. If prior art predates the filing date and discloses similar compounds or methods, validity could be challenged, especially if the claims are overly broad or lack inventive step.

5. What are key considerations for non-practicing entities (NPEs) assessing CN112955157?
They should analyze claim scope relative to their products, conduct freedom-to-operate searches, and evaluate potential infringement or licensing opportunities.


References

  1. China National Intellectual Property Administration (CNIPA). Patent CN112955157 metadata.
  2. Patent landscape reports on Chinese pharmaceutical patents, [industry reports].
  3. Comparative analysis of Chinese drug patent law and international standards.

This professional analysis aims to assist stakeholders in making data-driven strategic decisions regarding the patent CN112955157 and the broader Chinese pharmaceutical patent environment.

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