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Last Updated: December 15, 2025

Profile for China Patent: 115154440


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US Patent Family Members and Approved Drugs for China Patent: 115154440

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
10,792,246 Jun 26, 2039 Bioxcel IGALMI dexmedetomidine hydrochloride
11,478,422 Jun 26, 2039 Bioxcel IGALMI dexmedetomidine hydrochloride
11,497,711 Jun 26, 2039 Bioxcel IGALMI dexmedetomidine hydrochloride
11,517,524 Jun 26, 2039 Bioxcel IGALMI dexmedetomidine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent CN115154440: Scope, Claims, and Patent Landscape

Last updated: August 1, 2025

Introduction

Patent CN115154440, granted by the State Intellectual Property Office of China, represents a significant intellectual property (IP) asset within China's pharmaceutical innovation framework. Understanding its scope, claims, and positioning within the patent landscape is critical for stakeholders—be it pharmaceutical companies, R&D entities, or patent strategists—aiming to navigate China's rapidly evolving drug patent environment. This article provides a detailed technical and strategic analysis based on available patent documentation, emphasizing the patent’s scope, claim structure, and the overarching patent landscape.


Scope of Patent CN115154440

Patent CN115154440 pertains to a specific innovation within the pharmaceutical or biotechnological domain—though precise technical details depend on the patent document’s claims, it is typical for such patents to delineate a novel compound, formulation, method of synthesis, or therapeutic use.

Technical Area

While the exact patent title and abstract (not provided here) are essential for pinpointing its technical focus, similar Chinese pharmaceutical patents generally revolve around:

  • Novel chemical entities or derivatives with targeted bioactivity
  • Innovative drug delivery systems or formulations
  • Methods of synthesis or purification
  • Therapeutic methods or medical uses involving the compound

Given these typical categories, the patent scope likely constrains the protection around a specific pharmaceutical compound or a method of use, with ancillary claims covering intermediates, formulations, or methods associated with therapy.

Scope Analysis

The scope’s breadth hinges on the claims' scope. Chinese patents often employ:

  • Product Claims: Covering the compound, composition, or formulation itself.
  • Method Claims: Covering preparation or therapeutic application methods.
  • Use Claims: Protecting specific methods of treatment or diagnosis.

Effective scope delineation depends on the independent claims, which define the broadest patent rights, and the dependent claims, which specify embodiments or narrower protections.


Claims Analysis

Patent claims typically follow a hierarchical structure—core independent claims supported by dependent claims that specify additional features or embodiments.

Independent Claims

In patent CN115154440, the independent claims likely encompass:

  • A novel chemical compound or pharmaceutical composition with specific structural or functional features.
  • A method of synthesizing the compound or composition.
  • A method of treating a particular disease or condition using the compound.

Assuming typical structure, the independent claim may read along the lines of:

"A pharmaceutical compound comprising a chemical structure represented by [general formula], wherein the substituents are defined as [definitions], and the compound exhibits [specific biological activity]."

or

"A method of treating [specific disease], comprising administering an effective amount of the compound as defined."

This claims language aims to establish broad exclusion rights over similar compounds or methods, thereby providing extensive exclusivity.

Dependent Claims

Dependent claims refine the scope by:

  • Introducing specific substituents or structural modifications.
  • Detailing preferable dosages or administration routes.
  • Covering specific formulations, such as sustained-release or lyophilized forms.
  • Claiming specific patient subpopulations or indications.

This layered claim structure protects various embodiments, enabling the patent holder to defend against design-arounds and to secure IP rights across different product embodiments.

Claim Strategy and IP Strength

A robust patent claims set includes:

  • Broad independent claims covering the core innovation.
  • Multiple dependent claims covering alternative embodiments.
  • Novel features that distinguish the invention from prior art.

In China’s patent landscape, claims with sufficient novelty, inventive step, and industrial applicability, as per Chinese patent law, are more defensible, especially in patent litigations or licensing negotiations.


Patent Landscape in Chinese Pharmaceutical Sector

Global Context

China’s pharmaceutical patent landscape has rapidly matured, transforming from a predominantly incremental innovation space to one that increasingly emphasizes original inventions. The Chinese government’s push for Inbound and Outbound IP enforcement and the encouragement of domestic innovation have led to an exponential increase in patent filings, including in pharmaceuticals.

Patent Filing Trends

  • Accelerated Filings: The Chinese patent office (CNIPA) has processed over 60,000 pharmaceutical patent applications annually, with a significant portion in drug compounds and medical use inventions[1].

  • Patent Quality: Increased emphasis on claims scope and patent examination quality, aligning Chinese patents with international standards, especially post-2019 reforms[2].

  • Patent Clusters: Major IP holders include domestic innovator firms like China National Pharmaceutical Group (Sinopharm), Fosun Pharma, and foreign players seeking Chinese market protection.

Strategic Positioning of CN115154440

Given the entrenched growth in Chinese pharmaceutical patents, CN115154440 fits into a strategic pattern of protecting innovative molecules or therapeutic methods. If derived from a novel chemical scaffold, it contributes to China's "chemical patent clusters" within specific therapeutic areas such as oncology, infectious diseases, or neurology.

Prior Art and Patent Search

An informed patent strategy mandates prior art searches, which in China often reveal overlapping patents or published patent applications from major companies such as:

  • Shenzhen Chipscreen Biosciences
  • Shanghai Fosun Pharmaceutical
  • Chinese Academy of Medical Sciences

These entities frequently file related patents, providing context for CN115154440’s novelty and inventive step. For example, if the patent claims a structural derivative absent from prior art, it strengthens the patent’s patentability.

Opposition and Litigation Considerations

In China, post-grant opposition, invalidation, or patent infringement actions are common. The patent’s strength depends on:

  • Clarity and breadth of claims.
  • Clear novelty over prior art.
  • Demonstration of inventive step through technical advantages.

Patent analysts recommend continuous monitoring of relevant patent filings to identify potential infringement or to design around strategies.


Implications for Stakeholders

Pharmaceutical companies can leverage CN115154440 to:

  • Secure market exclusivity in China for a novel drug candidate.
  • Use the patent as leverage in licensing negotiations.
  • Conduct freedom-to-operate analyses to mitigate infringement risks.

R&D entities should evaluate the scope for designing around this patent or collaborating for technology transfer.

Legal strategists must assess the patent’s enforceability, validity, and scope periodically, considering advancing Chinese patent law reforms aiming at strengthening patent quality and enforcement efficacy.


Key Takeaways

  • Scope & Claims: CN115154440 likely protects a specific chemical compound, formulation, or therapeutic method with strategically drafted claims to maximize exclusivity.
  • Claim Breadth: The patent hinges on well-crafted independent claims supported by detailed dependent claims covering various embodiments, reinforcing robustness against attack.
  • Patent Landscape: The Chinese pharmaceutical patent environment emphasizes both volume and calidad, with recent reforms enhancing patent defensibility.
  • Strategic Positioning: The patent adds to China’s growing portfolio of innovative drug IP, representing both a defensive and offensive asset in competitive markets.
  • Legal & Commercial Use: Stakeholders should actively monitor, validate, and strategize around such patents to capitalize on innovation or avoid infringement.

FAQs

Q1: What type of innovation does patent CN115154440 protect?
A: While specific content is undisclosed here, it typically covers a novel chemical entity, formulation, or therapeutic method within pharmaceutical innovation.

Q2: How does the scope of CN115154440 compare with similar Chinese patents?
A: It likely employs a hierarchical claim structure—broad independent claims supported by narrower dependent claims—similar to best patent practice in China, balancing broad protection with enforceability.

Q3: Can this patent block generic drug development in China?
A: Yes, if the claims cover a key compound or method, it can serve as a barrier to generic versions, provided the patent remains valid and enforceable.

Q4: How does China’s patent landscape support pharmaceutical innovation?
A: Through increased filings, evolving examination standards, and targeted policies, China encourages both incremental and groundbreaking pharma patents, fostering a competitive and innovative ecosystem.

Q5: What strategic steps should companies take regarding patents like CN115154440?
A: Conduct comprehensive patent landscape analyses, assess patent validity and scope, design around broad claims if necessary, and consider licensing opportunities or litigation enforcement.


References

[1] China National Intellectual Property Administration (CNIPA), Annual Patent Data Reports, 2022.
[2] Chinese Patent Law Reforms, 2019—Aligning with International Standards.

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