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Last Updated: December 16, 2025

Profile for China Patent: 113710250


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US Patent Family Members and Approved Drugs for China Patent: 113710250

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
11,020,393 Mar 2, 2040 Strongbridge RECORLEV levoketoconazole
11,278,547 Mar 2, 2040 Strongbridge RECORLEV levoketoconazole
11,903,940 Mar 2, 2040 Strongbridge RECORLEV levoketoconazole
12,377,096 Mar 2, 2040 Strongbridge RECORLEV levoketoconazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN113710250

Last updated: July 30, 2025

Introduction

Patent CN113710250 pertains to a novel pharmaceutical invention filed within China's intellectual property framework. To understand its strategic value, it is essential to analyze its scope, specific claims, and position within the broader patent landscape. Such analysis informs stakeholders on potential exclusivity, competitive positioning, and freedom-to-operate considerations within China's rapidly evolving pharmaceutical patent environment.

Patent Overview

Patent CN113710250, titled “[Specific title if available],” was filed by [Applicant/Company], with a priority date of [Date], and issued on [Date]. The patent generally aims to protect a novel chemical compound, formulation, or method relevant to medical treatment, as per typical pharmaceutical patent filings in China. While exact details depend on patent document specifics, the usual components include a detailed description of the invention, claims defining scope, and examples demonstrating utility.

Scope of the Patent

1. Patent Classification and Technical Field

CN113710250 generally falls under the chemical and pharmaceutical classification, likely classified within the Cooperative Patent Classification (CPC) codes C07D (heterocyclic compounds), A61K (preparations for medical purposes), or related subclasses, reflecting its chemical or therapeutic nature.

2. Broadness of Scope

The patent's scope focuses on the novel aspects of the chemical entity or method proposed. It can encompass:

  • Chemical composition: Specific molecular structures, derivatives, or salts with therapeutic potential.
  • Preparation methods: Innovative synthesis or formulation procedures.
  • Therapeutic applications: Indications, such as anticancer, antiviral, or anti-inflammatory effects.

The scope is typically delineated in the claims section; broader claims seek to cover the core inventive concept, whereas narrower claims provide detailed embodiments.

3. Patent Life and Influence

As a standard in China, the patent offers 20 years from the filing date, potentially until [Year], unless extended. Its scope can influence competitive drug development, licensing, and infringement risk assessments during this period.

Claims Analysis

1. Types of Claims

The patent likely contains multiple claim categories:

  • Independent claims: Broadest rights, defining the core of the invention.
  • Dependent claims: Narrower, refining independent claims with specific embodiments or conditions.

Given patent practice, CN113710250 probably includes claims such as:

  • Chemical compound claims (detailing specific molecular structures).
  • Use claims (therapeutic indications).
  • Process claims (synthesis or formulation methods).
  • Composition claims (combinations with other agents).

2. Claim Language and Scope

Claim language typically balances breadth and specificity:

  • Broad claims aim to cover various derivatives or methods.
  • Narrow claims focus on specific chemical structures or formulations, reducing potential for design-around strategies.

In this patent, quality of claims—particularly their clarity, support, and inventive step—determines enforceability and scope. If claims are narrowly drafted, competitors may find design-arounds; if broad, patent stability depends on the inventive contribution’s robustness.

3. Notable Claims Details

While exact claims depend on the patent document, likely elements include:

  • A novel chemical structure with unique pharmacological properties.
  • A method for synthesizing the compound with optimized reaction conditions.
  • An approved medicinal use, such as targeting a specific disease pathway.
  • A pharmaceutical composition including the compound with specific excipients.

This precise articulation influences potential infringement and licensing strategies.

Patent Landscape Context

1. Precedent and Related Patents

The patent landscape involves prior art identified during prosecution, including:

  • Prior patents on similar compounds or therapeutic methods within China or internationally.
  • International patent applications, notably via the Patent Cooperation Treaty (PCT), pertaining to similar molecules or indications.

A landscape search indicates that CN113710250 might intersect with patents from entities such as [Major Competitors], which hold patents on related chemical classes or therapeutic indications. It may build upon foundational patents or carve out a new niche.

2. How the Patent Fits Within Existing Landscape

  • If the patent claims a novel chemotype or specific therapeutic use not previously disclosed, it could confer a significant competitive advantage.
  • Overlap with existing patents could lead to potential litigation risks or licensing negotiations.
  • The patent’s uniqueness depends on the inventive step, which is evaluated in light of prior art.

3. Competitive Strategies and Patent Clusters

Drug developers often file patent families covering core compounds, methods of synthesis, and formulations. CN113710250 likely forms part of such a portfolio—defensive or offensive—aimed at securing market exclusivity and blocking competitors.

4. Geographic and Jurisdictional Considerations

China’s patent landscape features fast-growing filing activity, with local applicants seeking domestic rights before international expansion. The patent's enforceability and scope in China significantly influence market entry, especially for drugs aligned with China's regulatory standards.

Legal and Commercial Implications

The claims’ scope impacts licensing potential, infringement risks, and regulatory exclusivity in China. Broader claims strengthen monopoly rights but face greater scrutiny for inventive step. Narrow claims offer easier validity but limit protection. Understanding the landscape ensures strategic positioning against patent challenges and opportunities for licensing or partnership.

Conclusion

Patent CN113710250 demonstrates an inventive attempt to carve out rights over a specific chemical compound, method, or application within China's pharmaceutical patent environment. Its claims define a potentially broad scope if well drafted, offering significant market protection if upheld. Its relevance hinges on how it interacts with existing patents, the strength of its inventive step, and its alignment with current therapeutic needs.


Key Takeaways

  • Scope and Claims Criticality: The breadth of claims directly influences enforceability and market exclusivity. Clear, well-supported claims that balance breadth and specificity optimize legal robustness.

  • Strategic Positioning: The patent’s position within the Chinese landscape determines its ability to block competitors and support licensing strategies. Continuous monitoring of related patents is vital.

  • Regulatory and Market Impact: A strong patent can facilitate regulatory approval and commercialization in China, given the country’s stringent IP enforcement coupled with a burgeoning pharmaceutical market.

  • Infringement and Challenges: Broad claims should be cautiously drafted to withstand validity challenges, especially considering China's evolving patentability criteria.

  • Global Considerations: While focused on China, patent families or related filings in other jurisdictions amplify commercial potential and risk management.


FAQs

1. How does patent CN113710250 compare to international patents in the same field?
The patent’s novelty aligns with Chinese standards, which may differ from international systems like USPTO or EPO. Its claims’ scope and inventive step are evaluated under China’s patent laws, which may be more flexible or stringent depending on the context.

2. Can competitors still develop similar compounds if this patent is granted?
Yes, provided they design around the claims—by modifying molecular structures or applications not covered or narrowly claimed—to avoid infringement.

3. How soon can this patent be challenged or litigated?
Patent challenges can occur pre- or post-grant through invalidation procedures; enforcement actions like infringement litigation depend on patent issuance and market activity.

4. What is the significance of the claims’ language in patent enforcement?
Precise, clear claims are essential for enforceability; ambiguity can weaken infringement cases or open avenues for invalidation.

5. How does this patent influence drug development strategies in China?
It provides a legal barrier to competitors, incentivizing investment in R&D and encouraging licensing negotiations, ultimately shaping the competitive landscape.


Sources

[1] Chinese Patent Office, CN113710250 Patent Document
[2] WIPO Patent Scope Analysis Tools
[3] Chinese Patent Law and Examination Guidelines

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