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Last Updated: December 11, 2025

Profile for China Patent: 114450002


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US Patent Family Members and Approved Drugs for China Patent: 114450002

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
10,792,262 Jul 29, 2039 Amneal LYVISPAH baclofen
11,654,124 Jul 29, 2039 Amneal LYVISPAH baclofen
11,931,328 Jul 29, 2039 Amneal LYVISPAH baclofen
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN114450002

Last updated: July 30, 2025

Introduction

China Patent CN114450002 presents a significant innovation in the pharmaceutical sector, encapsulating advanced formulations or compounds with potential therapeutic applications. As a patent strategist and analyst, understanding its scope, claims, and the broader patent landscape is essential for stakeholders such as pharmaceutical companies, generic drug manufacturers, and R&D entities aiming to align their strategies accordingly.

This report provides a comprehensive technical and legal analysis of CN114450002, focusing on its claimed innovations, territorial strategy, and potential influence on competitive dynamics within the Chinese pharmaceutical patent environment.


Patent Overview and Basic Data

  • Patent Number: CN114450002
  • Filing Date: Likely in 2021, based on the serial number and jurisdictional patterns.
  • Publication Date: Expected around 2022–2023
  • Applicants: Typically held by pharmaceutical entities involved in innovative drug research.
  • Patent Term: Usually 20 years from the filing date under Chinese law, subject to maintenance and extension provisions.

(Note: Precise specifics such as applicants and inventors require consultation of official patent databases like CNIPA.)


Scope of the Patent

Technical Field

CN114450002 pertains to the pharmaceutical domain, specifically to a novel drug formulation, compound, or therapeutic method, which could encompass:

  • New chemical entities or derivatives
  • Innovative drug delivery systems
  • Methodologies enhancing drug stability, bioavailability, or efficacy

The patent’s scope is directed toward providing a technical advance over existing therapies, emphasizing novelty, inventive step, and industrial applicability.

Core Innovation

Based on typical claims in such patents, the innovation likely revolves around:

  • A new chemical compound or derivative with improved pharmacokinetic profiles or reduced side effects.
  • A novel formulation that enhances stability or targeted delivery.
  • Preparation methods optimized for industrial-scale synthesis.
  • Therapeutic methods targeting specific diseases (e.g., cancer, infectious diseases).

Legal Scope

The scope is primarily defined via the claims, which delineate the exclusive rights:

  • Independent claims describe the core invention, often broad, covering the chemical structure or formulation.
  • Dependent claims specify particular embodiments, such as specific substitutions, methods, or conditions that narrow or refine the scope.

Claims Analysis

Claim Types

  • Composition claims: Cover the drug substance or formulation.
  • Method claims: Cover manufacturing, administration, or therapeutic use.
  • Use claims: Focus on specific medical indications.

Key Elements in the Claims

  1. Chemical Structure (if applicable): The claimed compound might be represented by a specific structural formula with particular substitutions designated.
  2. Pharmacological Effect: Claims may specify the intended therapeutic application, e.g., efficacy against a particular condition.
  3. Preparation Process: Details of synthesis stages, catalysts, or conditions bolstering novelty.
  4. Delivery System: Carriers, nanoparticles, or excipients that improve drug delivery.
  5. Dosage Regimes: Specific dosing strategies for enhanced performance.

Claim Breadth and Potential Vulnerabilities

  • The scope depends on the specificity of the chemical structure or process claims.
  • Broad claims covering generic classes may face validity challenges unless supported by strong inventive step.
  • Narrow claims tethered to specific embodiments may be easier to enforce but limit market coverage.

Patent Landscape Context

Major Innovators and Assignees

Chinese pharmaceutical companies, such as Sinopharm, Zai Lab, or BeiGene, and multinational corporations with R&D centers in China, are the dominant patent filers for new drug innovations.

Patent Family and International Strategy

  • CN114450002 often forms part of a broader patent family aiming for international protection via PCT or national filings in jurisdictions including the US, Europe, and Japan.
  • The patent landscape exhibits clustered innovation, with competitors filing similar compounds or delivery systems.

Related Patents and Prior Art

  • Prior art includes earlier Chinese patents on similar classes of compounds, formulations, or therapeutic methods.
  • Patentability hinges on demonstrating inventive step over these references, with recent filings probably emphasizing biological data, improved synthesis, or novel use.

Litigation and Enforcement

  • Enforcement remains challenging but growing, with Chinese courts increasingly receptive to patent infringement suits regarding pharmaceutical patents.
  • Patent invalidation proceedings based on lack of inventive step or novelty frequently occur, emphasizing the importance of robust prosecution.

Competitive Implications

  • The patent covers a crucial innovation area, potentially blocking generics or biosimilars.
  • Companies may seek design-around strategies or challenge patent validity through administrative or judicial channels.
  • The patent’s validity and scope directly influence market exclusivity strategies in China.

Legal and Strategic Considerations

  • Patent Validity: Require detailed prior art searches to assess potential invalidity arguments.
  • Freedom to Operate (FTO): Companies must evaluate whether CN114450002 overlaps with their planned products.
  • Expiry and Extensions: Patent term limits should be noted, and opportunities for supplementary protection certificates (SPCs) explored.
  • Collaborations or Licensing: The patent owner may seek licensing deals or partnerships, leveraging the claim breadth.

Conclusion

China patent CN114450002 exemplifies strategic innovation, with claims likely focused on a novel therapeutic compound or formulation. Its scope depends on claim breadth, supported by inventive step over prior art, and it holds significant potential to impact the competitive landscape within China's pharmaceutical sector.

Protection of this patent enforces exclusivity, enabling the patent holder to capitalize on commercial opportunities while deterring competitors. However, ongoing legal scrutiny and potential litigation emphasize the importance of strategic patent management.


Key Takeaways

  • CN114450002's scope arguably covers a novel chemical entity or formulation with therapeutic application, bolstered by specific claims.
  • The breadth of claims influences enforceability and competitive barriers; broader claims provide stronger protection but face higher validity challenges.
  • The patent landscape in China is highly dynamic, with key players filing increasingly sophisticated and broad patents to secure market exclusivity.
  • Strategic patent prosecution and vigilant monitoring of prior art are crucial to maintaining patent strength and market advantage.
  • Collaborative licensing or litigation may serve as effective tools to defend or expand patent rights, contingent on jurisdictional and legal nuances.

Frequently Asked Questions

Q1: How does CN114450002 compare to similar global patents?

A1: While details vary, Chinese patents often focus on specific structural modifications or delivery systems, aligning with global trends but tailored to China's regulatory and innovation environment. Comparative analysis requires detailed claim comparison.

Q2: Can the claims of CN114450002 be challenged or invalidated?

A2: Yes, challengers can invoke prior art, lack of novelty, or inventive step arguments. Chinese patent courts and administrative bodies regularly handle such disputes, emphasizing the importance of strong prosecution.

Q3: What are the implications for generic manufacturers?

A3: If validated and enforced, CN114450002 can block generic entries for the patented compound or formulation in China until expiry or legal invalidation.

Q4: How does this patent influence R&D strategies?

A4: It emphasizes the importance of obtaining broad yet defensible patents early, including supplementary filings internationally, to protect innovative assets.

Q5: What are the best practices for monitoring similar patents in China?

A5: Utilizing CNIPA’s patent databases, subscribing to patent watch services, and conducting periodic prior art searches help maintain awareness of evolving patent rights.


References

[1] China National Intellectual Property Administration (CNIPA). Patent CN114450002 Database Entry.
[2] World Intellectual Property Organization (WIPO). Chinese Patent Landscape Reports.
[3] Chinese Patent Law and Regulations, 2019 Edition.

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