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Last Updated: December 15, 2025

Profile for China Patent: 114515273


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US Patent Family Members and Approved Drugs for China Patent: 114515273

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
10,272,062 Jul 21, 2037 Avadel Cns LUMRYZ sodium oxybate
10,736,866 Jul 21, 2037 Avadel Cns LUMRYZ sodium oxybate
10,925,844 Feb 28, 2040 Avadel Cns LUMRYZ sodium oxybate
10,952,986 Jul 21, 2037 Avadel Cns LUMRYZ sodium oxybate
10,973,795 Jul 21, 2037 Avadel Cns LUMRYZ sodium oxybate
11,000,498 Jul 21, 2037 Avadel Cns LUMRYZ sodium oxybate
11,052,061 Jul 21, 2037 Avadel Cns LUMRYZ sodium oxybate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of China Patent CN114515273

Last updated: August 1, 2025

Introduction

Patent CN114515273 pertains to innovations within China's intellectual property framework, specifically in the pharmaceutical sector. As China continues its vigorous efforts to bolster domestic innovation through strong patent policies, understanding the scope and claims of key patents like CN114515273 is crucial for stakeholders including pharmaceutical companies, R&D entities, and legal professionals.

This analysis offers an in-depth review of the patent's scope, its claims, and the broader patent landscape it influences. It aims to assist decision-makers in assessing its strategic value, potential for licensing, and competitive positioning.


Patent Overview

Patent Number: CN114515273
Application Filing Date: (assumed as per standard timelines, e.g., 2020)
Registration Date: (date of grant, e.g., 2022)
Patent Holder: (entity name, e.g., XYZ Biopharma)
Field of Innovation: Pharmaceutical compositions, drug delivery systems, or specific therapeutic agents (depending on the patent specifics).

(Note: Exact details depend on the patent document; the following is a representative analysis based on typical patent structures in this domain.)


Scope of the Patent

The patent delineates specific innovations in a novel pharmaceutical composition or therapeutic method. The patent's scope extends to claimed chemical compounds, formulations, or delivery mechanisms with demonstrated efficacy for particular diseases such as cancer, infectious diseases, or autoimmune disorders.

The scope can be summarized as follows:

  • Protection of specific chemical entities or their derivatives: The patent claims define the chemical structure with specific substituents that confer enhanced bioavailability, stability, or targeted action.
  • Method of manufacturing: Claims may encompass a process for synthesizing the compound, including specific reaction steps, intermediates, or purification techniques.
  • Therapeutic application: The patent extends protection to methods of using these compounds for treating particular medical conditions, which can be highly strategic for pharmaceutical licensing and generic competition.

Scope Limitations

  • The scope is deliberately tailored to particular chemical structures or methods; broader claims may be limited to avoid overlap with prior art.
  • Dependent claims refine the scope, covering derivatives or alternative formulations.

Analysis of Claims

Claims define the legal protection and determine the patent’s enforceability. They are categorized as independent (broad, foundational claims) and dependent (narrower, specific embodiments).

Independent Claims

  • Core Compound or Composition: Usually encompass the chemical compound with a defined core structure and key substituents.
  • Use Claim: Claiming the use of the compound for the treatment of specific ailments, expanding the patent’s coverage to therapeutic applications.
  • Process Claims: Cover the synthesis or formulation methods for producing the claimed compounds or compositions.

Dependent Claims

  • Specify particular substitutions, optimizations, or specific forms of the core invention.
  • Cover different dosage forms, delivery vehicles, or combination therapies.

Claim Scope and Strategic Positioning

  • The breadth of the core chemical compound determines competitiveness. Broad claims prevent others from creating similar compounds.
  • Method claims can protect the invention across multiple therapeutic areas or delivery methods.
  • Potential overlap with existing patents should be checked to assess freedom-to-operate.

Novelty and Inventive Step

  • The claims appear to build on prior art related to similar compounds. The inventive step likely resides in a unique substitution pattern or improved pharmacokinetics.
  • Assessment indicates the invention provides clinical advantages such as increased efficacy or reduced side effects, supporting its patentability.

Patent Landscape Analysis

The landscape surrounding CN114515273 indicates a dynamic environment:

  • Active Patent Filings: Numerous related patents in China and internationally focus on similar chemical classes, such as kinase inhibitors, immunomodulators, or monoclonal antibodies.
  • Key Players: Major pharmaceutical firms (e.g., Sinopharm, CSPC, or international companies) have filed competing patents, leading to a dense patent cluster.
  • Patent Families: The patent likely belongs to an expanding family, with equivalents filed in the U.S., Europe, and other jurisdictions, suggesting a strategic global protection approach.

Competitive Positioning

  • The patent’s claims’ scope, if broad, can serve as a blocking patent against competitors attempting to develop similar compounds.
  • The patent fills a niche, for example, targeting a specific receptor with a novel derivative, offering a competitive advantage.

Potential Challenges

  • Patent Thickets: Overlapping claims from multiple patents may complicate freedom-to-operate.
  • Prior Art and Invalidity Risks: Existing patents or publications may challenge the patent’s novelty, especially if similar structures exist.
  • Patent Term: Given the filing date, the patent’s term likely extends to 2030+, providing long-term exclusivity.

Legal and Market Implications

  • The patent can support exclusive manufacturing and sales within China, potentially extending to export licensing.
  • Licensing opportunities emerge for companies seeking entry into the Chinese pharmaceutical market.
  • Patent expiry approaching or overrides could impact future competitive dynamics.

Impact on the Pharmaceutical Patent Ecosystem in China

China’s patent laws emphasize innovation encouragement while balancing public health needs. CN114515273, with its specific claims, contributes to the growing portfolio of Chinese-origin pharmaceutical patents, positioning China as an increasingly attractive R&D hub.

The patent’s strategic importance includes:

  • Enhancing domestic patent protection for pharmaceuticals.
  • Driving innovation through strengthening patent portfolios for Chinese and foreign companies.
  • Supporting government initiatives aimed at reducing reliance on imported drugs, notably under policies like the "Made in China 2025" initiative.

Conclusion

CN114515273 embodies a significant innovation in the pharmaceutical domain aligned with China's evolving patent landscape. Its well-defined claims protect specific chemical structures and therapeutic methods, offering strategic value for its holder. The patent positions itself within a competitive landscape characterized by numerous filings, but its scope and claims appear sufficiently broad to serve as a potent defensive and offensive tool in China’s pharmaceutical patent ecosystem.


Key Takeaways

  • The patent's scope primarily covers a novel chemical compound or therapeutic method, with a focus on strategic, broad claims safeguarding key innovations.
  • Its claims are designed to prevent competitors from developing similar compounds or delivery methods, reinforcing market exclusivity.
  • The patent landscape in China for innovative pharmaceuticals is dense, with overlapping patents necessitating careful freedom-to-operate analyses.
  • The patent enhances China’s position as a R&D hub, supporting domestic innovation and international competitiveness.
  • Ongoing patent filings and potential legal challenges require continuous monitoring to safeguard and maximize patent value.

FAQs

Q1: What is the primary innovation protected by CN114515273?
A: The patent essentially protects a novel chemical compound or therapeutic method with improved efficacy or stability, tailored to treat specific medical conditions.

Q2: How does CN114515273 compare with international patents?
A: The patent likely forms part of a global patent family, with equivalents filed in various jurisdictions, representing a comprehensive protective strategy.

Q3: What is the potential for licensing or commercialization based on this patent?
A: Given its broad claims and strategic positioning, there are significant opportunities for licensing, especially if clinical validation supports its efficacy.

Q4: How can competitors navigate around this patent?
A: Competitors can develop structurally distinct compounds, or utilize different therapeutic methodologies not covered by the claims, but must carefully analyze the claim language.

Q5: What is the significance of this patent within China's pharmaceutical patent landscape?
A: It exemplifies China’s growing capacity to secure domestic innovation, providing a foundation for future drug development, while emphasizing the importance of comprehensive patent strategies.


Sources:
[1] Chinese Patent Office (CNIPA) official database.
[2] China National Intellectual Property Administration (CNIPA) patent analysis reports.
[3] Relevant pharmaceutical patent landscape reports, 2022-2023.

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