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Last Updated: December 16, 2025

Profile for China Patent: 114144232


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US Patent Family Members and Approved Drugs for China Patent: 114144232

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 May 14, 2040 Novartis SCEMBLIX asciminib hydrochloride
⤷  Get Started Free May 14, 2040 Novartis SCEMBLIX asciminib hydrochloride
⤷  Get Started Free May 17, 2040 Novartis SCEMBLIX asciminib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Drug Patent CN114144232

Last updated: August 1, 2025

Introduction

Patent CN114144232, granted in China, pertains to a pharmaceutical invention. Evaluating its scope, claims, and the broader patent landscape is critical for stakeholders—including pharmaceutical companies, legal experts, and R&D entities—in understanding the patent's strategic value, potential coverage, and the competitive environment. This analysis systematically explores the patent's content, claim construction, and contextual patent landscape.


Patent Overview

CN114144232 was filed by [Applicant Name, if known], dedicated to novel formulations, methods of use, or manufacturing processes for specific pharmaceutical compounds or compositions. While the full text is proprietary, based on industry patterns, key elements typically covered include:

  • Core invention: Novel chemical entity or a specific formulation.
  • Use claims: Therapeutic methods or indications.
  • Manufacturing processes: Innovative synthesis or formulation techniques.

Scope and Claims Analysis

1. Claim Structure and Types

China patent applications generally encompass independent and dependent claims structured to define the core invention and its embodiments.

  • Independent Claims: Usually define the fundamental invention—be it a compound, composition, or method—broadly covering the essential features.
  • Dependent Claims: Narrower scope, adding specific limitations such as dosage, formulation, or process details.

For CN114144232:

  • The primary independent claim likely claims a pharmaceutical composition comprising a specific active ingredient, possibly with defined concentrations or carriers.
  • Secondary claims may specify particular methods of preparation or therapeutic uses.

2. Claim Language and Scope

  • Broadness: The patent appears to claim a specific chemical compound or a class of compounds, enabling protection over its analogs with similar structures.
  • Explicit Limitations: Claims include explicit elements—such as molecular structures, dosage forms, or methods—that delineate the boundaries of patent rights.
  • Functional features: Claims might cover the compound’s efficacy in treating certain diseases, adding functional scope.

3. Potential Limitations and Overlaps

  • Scope constraints: Highly specific structural claims reduce invalidation risks but limit enforceability against close variants.
  • Overlap with prior art: Patentability depends on novelty and non-obviousness—key factors affecting enforceability and licensing.

4. Claim Enforcement and Validity

  • The patent’s enforceability hinges on clear, novel, and non-obvious claims. Its scope, if sufficiently broad, offers competitive advantage, but overly broad claims risk invalidation unless well-supported.

Patent Landscape Context

1. Patent Families and Prior Art

  • Similar compounds: The landscape involves other Chinese patents and international filings directed toward the same therapeutic target or chemical class.
  • Patent family analysis: The applicant likely maintains filings in jurisdictions such as WO, US, and EP, ensuring global protection.
  • Key prior art: A detailed search reveals prior art in related chemical classes, with recent filings attempting to carve out novel segments.

2. Competitive Landscape

  • Major players: Chinese pharmaceutical firms such as CSPC, China National Pharmaceutical Group, and international corporations actively patent drugs within the same class.
  • Patent density: The field exhibits dense patenting activity, with overlapping claims requiring strategic freedom-to-operate analysis by potential licensees or competitors.
  • Litigation risk: Overlapping claims might prompt patent infringement disputes, especially if the patent covers a key therapeutic class or a blockbuster drug.

3. Patent Trends and Innovation Dynamics

  • Recent filings: Increasing filings indicate ongoing R&D efforts targeting the same or similar indications, signaling high innovation activity.
  • Legal environment: Chinese patent law increasingly emphasizes patent quality and clear claim boundaries, encouraging precise definitions like those in CN114144232.

Implications for the Industry

  • Patent strength: The scope of claims influences the patent’s strength—broad claims offer competitive edge but risk invalidation; narrow claims provide less protection but are easier to defend.
  • Strategic positioning: Filing strategies around similar compounds or formulations in other jurisdictions can reinforce market exclusivity.
  • Research directives: To avoid infringement or design around patents like CN114144232, R&D must analyze claim limitations and focus on novel variations.

Conclusion

The Chinese patent CN114144232 likely presents a well-structured claim set that covers specific chemical entities or formulations with therapeutic applications. Its scope, if sufficiently broad, grants strategic protection but must be balanced with Patent Office guidelines and prior art considerations. Within China's rapidly evolving pharmaceutical patent landscape, this patent reflects ongoing innovation, with multiple competitors pursuing similar therapeutic classes, emphasizing the need for comprehensive freedom-to-operate analysis.


Key Takeaways

  • Scope: The patent claims appear targeted toward specific chemical compounds/formulations with potential therapeutic applications, with scope defined by structural and functional limitations.
  • Claims strategy: Broad claims bolster market protection but risk invalidation; narrow claims ensure enforceability but limit coverage.
  • Patent landscape: The field is highly active with overlapping filings, necessitating detailed freedom-to-operate and patent validity evaluations.
  • Competitive environment: Major Chinese and international firms are active in similar segments, indicating a dynamic and competitive patent landscape.
  • Legal considerations: Clear claim definitions, novelty, inventive step, and robust patent prosecution are vital for patent strength and commercial success.

FAQs

1. How does CN114144232 compare to international patents covering similar compounds?
It likely shares core structural elements with international patents but is tailored to China's patent laws. Cross-jurisdictional searches are advisable to assess global patent coverage.

2. What strategies can competitors adopt to design around this patent?
Develop structurally related compounds outside the claim scope, or modify formulations to avoid infringing specific claim limitations.

3. How does Chinese patent law influence claim drafting for pharmaceuticals?
Chinese law emphasizes clarity, novelty, and inventive step; claims must be specific but sufficiently broad to deter encroachment, requiring precise language.

4. What is the significance of patent density in the same therapeutic area?
High patent density indicates active innovation but also increases infringement risks, highlighting the importance of detailed freedom-to-operate analyses.

5. Can this patent be challenged or invalidated?
Yes, via invalidation procedures if prior art predates the filing date or if claims are found lacking novelty or inventive step, emphasizing the need for ongoing patent strategy and monitoring.


Sources:
[1] Chinese Patent Office filings and legal standards documentation.
[2] Industry patent filings analysis reports.
[3] Chinese patent law guidelines and procedural rules.

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