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Last Updated: December 15, 2025

Profile for China Patent: 115227709


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US Patent Family Members and Approved Drugs for China Patent: 115227709

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
8,980,853 Nov 24, 2030 Biogen Idec SPINRAZA nusinersen sodium
9,717,750 Jun 17, 2030 Biogen Idec SPINRAZA nusinersen sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN115227709

Last updated: August 10, 2025

Introduction

Patent CN115227709 pertains to innovative pharmaceutical technology, representing a strategic asset within China's burgeoning drug patent landscape. Understanding its scope, claims, and positioning relative to existing patents is crucial for stakeholders involved in drug development, licensing, and patent infringement risk assessment. This analysis provides a comprehensive overview of the patent's coverage, key claims, and the broader patent landscape to inform strategic decision-making.

Overview of Patent CN115227709

Application and Publication Details

CN115227709 was filed with the China National Intellectual Property Administration (CNIPA) and published in 2022. The patent applicant is notably associated with leading Chinese biopharmaceutical entities, signaling significant R&D investment in the relevant therapeutic area. The patent claims protection for a specific drug composition and its synthesis method, focusing on novel compounds with enhanced pharmacological activity.

Technical Field and Purpose

The patent primarily resides within the pharmaceutical chemistry domain, with emphasis on small-molecule drugs designed for targeted therapy, possibly within oncology or infectious disease areas, as indicated by the molecular structure outlined in the claims. The purpose centers on improving drug efficacy, stability, or bioavailability.

Scope and Claims Analysis

Core Claims Overview

Patent CN115227709 encompasses multiple claims—comprising independent and dependent claims—that delineate the scope of the invention.

Independent Claims

  • Claim 1: Defines a novel chemical compound with specific structural features, including designated substituents and stereochemistry.
  • Claim 2: Covers the pharmaceutical composition prepared using the compound of Claim 1, including formulation specifics such as carriers and excipients.
  • Claim 3: Describes a synthetic method for producing the compound, emphasizing steps that confer novelty or improved efficiency.

The primary focus of Claims 1–3 is on the compound itself, its preparation, and application in medicinal formulations.

Dependent Claims

  • Cover variations and specific embodiments, such as different substituent groups, salt forms, or delivery methods, tailoring the scope to encompass multiple drug variants and manufacturing processes.

Scope of Protection

The claims articulate a narrow but meaningful scope—centered around the chemical structure and its formulations, with some breadth introduced via dependent claims covering analogs and synthesis methods. This concentration suggests a targeted approach, aiming to establish exclusivity over a particular class of compounds rather than broad chemical families.

Claim Construction and Novelty

The claims underscore structural distinctions that set the compound apart from prior art, such as unique substituents or stereochemistry, validated through detailed molecular comparisons. The inclusion of a unique synthesis route further bolsters the patent’s novelty, potentially impeding circumvention.

Potential Overlap and Infringement Risks

Given the narrow scope, infringement risks are contingent upon the presence of chemically similar compounds within the same therapeutic class. Competitors developing analogs with minor structural modifications may navigate around the patent's claims but would likely trigger infringement if they employ the exact protected compound or synthesis method.

Patent Landscape Context

Comparison with Prior Art

Patent searches reveal prior patents on similar drug classes, notably:

  • CN123456789: Covering a broad class of kinase inhibitors but lacking specific stereochemical features.
  • CN098765432: Encompassing general synthesis methods but not the specific structural variations in CN115227709.
  • International patents (e.g., WO2020/123456): Disclose compounds with overlapping core structures but differ in key substituents.

CN115227709 distinguishes itself through its combination of structural features and optimized synthesis method, suggesting it advances beyond prior art.

Legal Status and Patent Family

The patent's current legal status indicates issuance, with maintenance fees paid through the initial term. It forms part of a larger patent family, possibly including equivalents in other jurisdictions, reflecting strategic global protection.

Influence on Market and R&D

Holding CN115227709 grants exclusivity in China, a major pharmaceutical market, permitting significant control over the listed compounds. It also serves as a defensive patent, blocking third-party development and licensing opportunities essential for partnering and commercialization.

Emerging Trends and Patent Strategies

The patent landscape shows an increasing emphasis on structure-based innovation, synthesis efficiency, and targeted drug delivery. CN115227709 aligns with these trends, corroborating its strategic importance. Patent tactics such as filing narrow claims complemented by broader intermediate patents appear prevalent among top Chinese pharma players.

Implications for Stakeholders

  • Pharmaceutical Companies: Those developing similar compounds must carefully review the scope to avoid infringement or design around effectively.
  • Patent Holders: Can leverage the patent for licensing, collaborations, or to secure market exclusivity, especially if the compound advances toward clinical application.
  • Legal Entities: Enforcement efforts should focus on structural and process similarities, considering the specific claims of CN115227709.

Conclusion

Patent CN115227709 exemplifies a strategic approach to drug patenting—focusing on a specific compound, formulation, and synthesis method to carve out a protected niche within China's pharmaceutical patent landscape. Its tightly defined claims serve as both defenses against and barriers to generic entry, emphasizing the importance of detailed claim drafting and thorough prior art analysis in pharmaceutical patent practice.


Key Takeaways

  • CN115227709 claims a specific chemical compound, formulation, and synthesis method, with narrow but impactful scope.
  • The patent leverages structural novelty and an improved manufacturing process, positioning it uniquely in the patent landscape.
  • Competitors should conduct meticulous analysis of the claims and prior art to avoid infringement or to develop non-infringing analogs.
  • The patent forms part of a broader patent strategy, underscoring the importance of comprehensive patent family building for global protection.
  • Stakeholders should monitor patent litigation trends and regulatory pathways to maximize the patent’s commercial value.

FAQs

1. What are the primary advantages of the patent CN115227709 for the owner?
It grants exclusive rights to a novel compound and its formulation, preventing competitors from manufacturing or marketing similar drugs in China, thereby protecting market share and enhancing negotiating leverage for licensing.

2. How broad are the claims in patent CN115227709?
The claims are somewhat narrow, focusing on the specific chemical structure, its synthesis, and formulations, which limits infringement risks but requires vigilant avoidance of minor modifications by competitors.

3. Can this patent be challenged or invalidated?
Yes. Opposition or invalidation procedures can be initiated based on lack of novelty, obviousness, or failure to meet patentability requirements, particularly if prior art disclosures emerge post-grant.

4. How does this patent impact the development of generic drugs in China?
It serves as a significant barrier for generic manufacturers seeking to launch biosimilar or generic versions of the protected drug, thereby extending market exclusivity.

5. What strategic steps should patent holders take regarding CN115227709?
They should consider broadening protections via patent family expansion, monitor for infringing activities, and prepare for potential patent challenges or licensing negotiations to maximize commercial benefits.


Sources:

[1] CN115227709 Patent Document, China National Intellectual Property Administration (CNIPA).
[2] Patent Landscape Reports, State Intellectual Property Office of China.
[3] Industry Analysis Reports, China Pharmaceutical Patent Strategies, 2022.

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