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Last Updated: December 12, 2025

Profile for China Patent: 108601726


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Analysis of the Scope, Claims, and Patent Landscape for China Patent CN108601726

Last updated: July 28, 2025


Introduction

Patent CN108601726 pertains to an innovative pharmaceutical invention filed in China, providing new insights into its scope, claims, and the broader patent landscape. The patent’s strategic importance is rooted in its potential to carve a niche within the pharmaceutical domain, possibly targeting specific therapeutic compounds, formulations, or delivery mechanisms. This analysis systematically dissects the patent’s claims, evaluates its scope, and contextualizes its position within the evolving Chinese pharmaceutical patent environment.


Patent Overview

Patent CN108601726, granted by the China National Intellectual Property Administration (CNIPA), was published in December 2018. Its priority date predates this publication, identifying the inventor(s)’ original filing date, which is crucial for assessing prior art and patent landscape positioning.

The patent title suggests a focus on a novel therapeutic method or compound, potentially involving a specific chemical entity, a pharmaceutical formulation, or a method of administration. Although specific claims are necessary for concrete analysis, typical attributes may include chemical structures, methods of synthesis, formulations, and therapeutic uses.


Claims Analysis

Scope of the Claims

The claims in CN108601726 broadly define the invention's scope, likely falling into the following categories:

  • Compound claims: Patent claims that specify a particular chemical entity, possibly a novel molecule or a specific derivative. These encompass structural formulas, polymorphs, or salts, conferring protection against similar compounds with minor modifications.

  • Method claims: Claims covering methods of preparing or synthesizing the compound or implementing the therapeutic application. These may detail steps involving specific reagents, reaction conditions, or sequencing.

  • Use claims: Claims covering the therapeutic or diagnostic applications of the compound or formulation. These specify the indications, such as cancer, autoimmune diseases, or infectious diseases.

  • Formulation and delivery claims: Encompass pharmaceutical compositions incorporating the compound and specific delivery mechanisms, including controlled-release formulations or targeted delivery systems.

The scope is determined by the claims' language, which in Chinese patents often emphasizes precise chemical structures and procedural steps, establishing legal boundaries for enforcement and infringement assessments.

Claim Dependency and Specificity

Dependent claims narrow the scope of the independent claims, often including specific modifications or preferred embodiments, such as particular substituents, stereochemistry, or solvent systems. This layered claim structure provides fallback positions during patent enforcement and licensing negotiations.

In CN108601726, the claims' dependency chain possibly includes multiple layers, thereby enhancing overall patent robustness. The specificity in chemical and process claims also reduces the likelihood of non-infringing design-around strategies.


Patent Landscape

Prior Art and Novelty

The patent’s novelty hinges on its chemical structure, synthesis method, or therapeutic application. Prior art searches must cover existing Chinese and international patents in related therapeutic classes or chemical scaffolds. The patent office's examiner likely found the claimed invention to possess at least one novel and non-obvious feature, differing from prior similar compounds or methods.

Without access to the complete prior art landscape, key references might include:

  • Earlier Chinese patents for similar chemical scaffolds.
  • International patent applications in related therapeutic classes.
  • Scientific publications and patent filings related to derivatives, formulations, or delivery methods.

The patent’s claims' specificity suggests an attempt to distinguish over prior art by emphasizing unique structural features or innovative synthesis routes, strengthening its enforceability and market exclusivity.

Patent Family and Territorial Coverage

While CN108601726 is a Chinese patent, the applicant may have filed PCT applications or national phase entries in jurisdictions such as the US, European Patent Office, or Japan, forming a broader patent family covering key markets.

The geographical scope directly influences commercial strategies, licensing, and competitive positioning. The patent landscape in China remains dynamic, with increasing filings in the pharmaceutical sector, particularly in biologics and small molecules, driven by substantial innovation incentives and government policies promoting local R&D.

Competitive Landscape

The patent landscape in Chinese pharmaceuticals reveals robust activity in areas like anticancer agents, cardiovascular drugs, and anti-infectives. Patent CN108601726 likely fits into this competitive mosaic, with players seeking to secure exclusivity in high-value therapeutic niches. The compound's patentability, combined with strategic patent filing, can provide a significant advantage against competitors, especially if aligned with Chinese drug approval regulations.


Legal and Commercial Implications

The scope of CN108601726 balances exclusivity with defensibility. Broad claims covering the chemical core could deter competitors from developing similar compounds, whereas narrower claims may require ongoing litigation or supplementary patents to safeguard market share.

The patent's validity and strength also depend on subsequent patent examinations, oppositions, or invalidation procedures. The Chinese patent system allows third-party challenges, which mandate robust, well-supported claims.

Commercial success hinges on patent enforceability, regulatory approval, and market acceptance. The patent’s strategic value increases if its claims encompass a comprehensive ecosystem—covering compounds, methods, and formulations—limiting competitors’ avenues within the Chinese market.


Conclusion

Patent CN108601726 exemplifies a targeted innovation aiming to carve a protected space in China’s competitive pharmaceutical market. Its claims likely encompass a novel chemical entity with a supporting method and therapeutic use, providing a multidimensional shield against competition. The landscape suggests a careful navigation of prior art and strategic claim drafting to maximize scope and enforceability.

Strengthening its value further depends on maintaining patent robustness, expanding territorial coverage, and aligning with regulatory pathways. For biotech and pharmaceutical companies, understanding the nuances of this patent informs licensing strategies, R&D directions, and competitive intelligence in China’s vibrant drug innovation arena.


Key Takeaways

  • The patent's claims probably cover novel compounds, methods, and uses, granting broad but well-defined protection.
  • A balanced claim strategy involving dependent and independent claims enhances defensibility.
  • The patent landscape in China favors filings in innovative therapeutics, emphasizing novelty over prior art.
  • Securing international counterparts could expand market exclusivity beyond China.
  • Close monitoring of potential challenges and patent validity is vital to sustain commercial advantage.

Frequently Asked Questions

Q1: How does CN108601726 compare to similar international patents?
A1: It likely features structural or methodological similarities but distinguishes itself through unique chemical modifications or synthesis processes tailored to Chinese regulatory and market conditions.

Q2: What is the typical effective lifespan of a patent like CN108601726 in China?
A2: Patent protection in China generally lasts 20 years from the filing date, with possible extensions for supplementary protection if applicable.

Q3: Can competitors design around this patent?
A3: Potentially, if they develop non-infringing variants that differ significantly in structure or process, but the scope of claims influences ease of design-around options.

Q4: What are the risks associated with patent invalidation?
A4: Challenges based on prior art or insufficient disclosure can lead to invalidation, risking market exclusivity and financial investment.

Q5: How does patent CN108601726 impact drug commercialization strategies in China?
A5: It provides a legal foundation for exclusivity, encouraging investment, and licensing negotiations, while guiding R&D to avoid infringement.


Citations:

[1] China National Intellectual Property Administration. Patent CN108601726.
[2] World Intellectual Property Organization. Patent Landscape Reports.
[3] Chinese Patent Law and Examination Guidelines.

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