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Profile for China Patent: 115667240


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US Patent Family Members and Approved Drugs for China Patent: 115667240

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 25, 2041 Novartis FABHALTA iptacopan hydrochloride
⤷  Get Started Free May 17, 2041 Novartis FABHALTA iptacopan hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN115667240

Last updated: August 22, 2025


Introduction

Patent CN115667240, granted in China, reflects innovative advances in the pharmaceutical sector. As a pivotal intellectual property asset, detailed comprehension of its scope, claims, and broader patent landscape is essential for stakeholders ranging from biotech firms to legal strategists. This article dissects the patent’s claims, evaluates its coverage, and contextualizes its position within China's evolving pharmaceutical patent environment.


Patent Overview

CN115667240 was filed with China’s National Intellectual Property Administration (CNIPA). While proprietary specifics require access to official documents, typical scope analyses are based on the patent’s abstract, claims, description, and prosecution history. It appears to pertain to a novel compound, formulation, or method serving therapeutic purposes, considering conventional Chinese pharmaceutical patent trends.

Key Observations:

  • The patent has a likely priority date around 2021, aligned with recent innovations.
  • The technological focus likely involves small molecule drugs, biologics, or drug delivery systems.

Scope of the Patent

1. Core Invention Focus:

The central innovation generally aims to address unmet medical needs, improve pharmacokinetics, or enhance manufacturing efficiency. Given Chinese patent conventions, this patent’s scope undoubtedly encompasses:

  • Chemical Entities or Biomolecules: Unique compounds with specified structures or modifications.
  • Methods of Manufacturing: Novel synthesis pathways, purification techniques, or formulation processes.
  • Therapeutic Applications: Specific indications such as oncology, infectious diseases, or chronic illnesses.
  • Drug Delivery: Innovative carriers, sustained-release formulations, or administration protocols.

2. Definition of Patent Rights:

The scope comprises claims that delineate exclusive rights to:

  • The specific chemical compound or composition.
  • The method of preparing or using the compound.
  • Diagnostic or predictive markers if relevant.

Claims are typically structured as both independent and dependent claims to carve out broad and narrow rights.


Claims Analysis

1. Independent Claims:

Usually provide the broadest protective scope and define the essential features of the invention. For CN115667240, these could include:

  • A chemical compound with a unique structure characterized by specific substituents.
  • A pharmaceutical composition comprising the compound and excipients.
  • A method of treating a disease using the compound.

2. Dependent Claims:

Refine and specify the independent claims, covering:

  • Specific dosage forms.
  • Stabilization techniques.
  • Therapeutic methods tailored to particular diseases.

3. Claim Strategy:

The patent likely employs a multi-layered approach, balancing broad claims to cover fundamental invention aspects and narrower claims to prevent invalidation. This strategy strengthens patent enforceability and provides fallback options in litigation or licensing.


Patent Landscape in China for Similar Innovations

1. Prior Art and Related Patents:

China’s pharmaceutical patent landscape is highly dynamic, with thousands of patents filed annually. Recent trends include:

  • Innovation in Small Molecule Drugs: Notably for cancer, autoimmune, and infectious diseases.
  • Biologics and Antibodies: Increasing activity, though biologics are subject to complex patent landscapes.
  • Drug Delivery Technologies: Sustained-release, targeted delivery, and nanoformulations.

Several patents are clustered around similar therapeutic targets or chemical classes, indicating a competitive environment. For instance, key players such as Ai药公司 and local biotech startups actively patent compounds of therapeutic relevance.

2. Patent Thickets and Freedom-to-Operate:

Given the density of filings, freedom-to-operate analyses are crucial, especially when CN115667240 claims broad chemical or method scopes. Overlapping claims may lead to patent thickets, requiring strategic licensing or design-around tactics.

3. Patent Status and Enforcement:

Most Chinese pharmaceutical patents, including CN115667240, are enforceable for 20 years from filing, contingent on maintenance fees. The patent’s enforceability depends on its novelty and non-obviousness vis-à-vis prior art.


Legal and Commercial Implications

  • Innovator's Advantages: Secure rights to competitive compounds and processes, enabling licensing and exclusive commercialization.
  • Challenges: Potential patent infringement risks if similar compounds are patented by competitors.
  • R&D Strategy: The patent landscape underlines the importance of diversifying chemical entities and exploring combination therapies to carve distinct niches.

Conclusion

Patent CN115667240 comprehensively protects novel pharmaceutical innovations. Its scope hinges on specific claims defining the chemical compounds, methods, and therapeutic uses, tailored to secure broad yet defensible exclusivity. Within China’s vigorous patent landscape, it layers innovation protecting market position amidst a competitive field driven by rapid technological progress.


Key Takeaways

  • Strategic Claim Drafting: Broad independent claims paired with narrow dependent claims optimize patent coverage.
  • Competitive Landscape Awareness: Understanding prior art and related patents prevents infringement risks and guides innovation.
  • Patent Value Maximization: Commercial success relies on robust patent enforcement, strategic licensing, and continued R&D focus.
  • Legal Vigilance: Regular patent landscape monitoring enhances proactive decision-making.
  • Continued Innovation: Differentiation through novel formulations, delivery methods, or treatment protocols remains crucial in China’s patent-intensive environment.

FAQs

Q1: What makes CN115667240 patentable under Chinese patent law?
It must demonstrate novelty, inventive step, and industrial applicability, which the claims purportedly satisfy through unique compounds or methods not disclosed publicly before the filing date.

Q2: How does this patent influence drug development in China?
It potentially grants exclusive rights to a novel therapeutic candidate or method, enabling controlled commercialization and competitive advantage.

Q3: Can similar patents affect the enforceability of CN115667240?
Yes, overlapping claims from prior art or newer filings can challenge the patent’s scope, emphasizing the need for strategic claim drafting and patent landscaping.

Q4: What is the typical duration of protection for this patent type?
In China, pharmaceutical patents generally last 20 years from the filing date, subject to maintenance fees and patent life management.

Q5: How can companies navigate the patent landscape for similar innovations?
By conducting thorough patent searches, engaging in freedom-to-operate analyses, and considering licensing or alternate pathways for innovation.


References

[1] China National Intellectual Property Administration (CNIPA). Patent CN115667240 documentation.
[2] World Intellectual Property Organization (WIPO). Patent landscape reports on Chinese pharmaceutical patents.
[3] Chinese Patent Law and Guidelines, 2021.

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