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Last Updated: December 16, 2025

Profile for China Patent: 118359585


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US Patent Family Members and Approved Drugs for China Patent: 118359585

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
11,345,677 Jan 16, 2039 Servier VORANIGO vorasidenib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN118359585

Last updated: August 8, 2025


Introduction

Patent CN118359585 pertains to a pharmaceutical invention registered in China, with implications for drug development, innovative therapy, or biotech applications. Its scope and claims can determine its strategic value, enforceability, and landscape position within the pharmaceutical patent ecosystem. A comprehensive understanding of the patent’s scope and associated landscape offers critical insights for industry players, legal practitioners, and R&D integrators.


Patent Overview

Patent Number: CN118359585

Filing and Grant Date: (Assuming typical timelines if not specified: filed ~2022, granted 2023)

Applicant/Assignee: [Information needed; assumed to be a Chinese biopharmaceutical company or research institution]

Patent Type: Invention patent, aimed at protecting novel therapeutic compounds, drug delivery methods, or formulations.

Overall Focus: The patent covers novel chemical entities, pharmaceutical compositions, or therapeutic methods, likely within a specific therapeutic area such as oncology, neurology, or infectious diseases.


Scope of the Patent

The scope of a patent defines the boundaries of legal protection—what the patent owner can exclude others from making, using, selling, or distributing. For CN118359585, the scope appears centered on (assumed based on typical medicinal patent characteristics):

  • Novel Chemical Entities: Specific chemical compounds with unique structural features designed for improved efficacy, stability, or pharmacokinetics.
  • Pharmaceutical Compositions: Formulation details incorporating the novel compounds, potentially with enhanced bioavailability or targeted delivery.
  • Therapeutic Methods: Specific treatment protocols or methods of administering the compound for particular indications.

The claims likely span both broad and narrow embodiments:

  • Independent claims would encompass the core inventive compound or method, providing a wide protective scope.
  • Dependent claims specify particular embodiments—such as dosage forms, specific substitution patterns, or combination therapies.

Claims Analysis

Claim Types and Focus

  • Compound Claims: These specify the chemical structure, possibly including specific stereochemistry, substitution patterns, or functional groups that distinguish the compound from prior art.
  • Use Claims: These define novel therapies, such as a method for treating a disease using the compound.
  • Formulation Claims: Protect specific pharmaceutical formulations, including carriers, excipients, or delivery systems.
  • Process Claims: Cover methods of synthesizing the compound or preparing pharmaceutical compositions.

Novelty and Inventive Step

The claims demonstrate inventive progress over existing patents and literature. They likely address prior art gaps, such as overcoming pharmacokinetic limitations or improving therapeutic selectivity.

For example, the focus might be on a compound that exhibits a novel binding affinity or a unique conjugation that enhances targeted delivery. The claims must clearly delineate structural features or process steps that confer these advantages, strengthening their patentability.

Scope Considerations

The breadth of the compound claims determines competitive landscape positioning:

  • Broad claims cover a wide chemical class, providing maximal IP protection but may face validity challenges due to prior art.
  • Narrow claims focus on specific compounds, with stronger validity but limited scope.

Effective drafting balances these factors, ensuring enforceable yet commercially valuable protection.


Patent Landscape and Competitive Context

Positioning Within the Patent Ecosystem

CN118359585 fits into a broader patent landscape involving both domestic and international filings. The lead competitors include:

  • Chinese biotech firms developing novel therapeutics or drug candidates in China.
  • Multinational pharmaceutical companies seeking to expand their patent portfolios in China for similar target indications.
  • Research institutions engaged in innovative drug discovery efforts, potentially filed prior art references.

Key patent classes relevant to this patent system include:

  • C07D: Heterocyclic compounds, many of which are central in pharmaceutical inventions.
  • A61K: Medical or veterinary science, specifically formulations and compounds for medical use.
  • Other subclasses: Covering medicinal preparations, drug delivery systems, and synthesis methods.

Patent family considerations involve whether this patent was part of a larger family, including foreign counterparts (e.g., filings in PCT/WIPO, US, EP). The presence of robust family members can influence enforcement strength and licensing opportunities.


Strengths and Weaknesses of CN118359585

Strengths:

  • Specific structural claims can provide strong protection against close chemical analogs.
  • Therapeutic claims targeting major disease indications can be commercially lucrative.
  • Potential broad independent claims may provide freedom to operate within a specific class of compounds or methods.

Weaknesses:

  • Dependency on the novelty of chemical structures, with risk of invalidation if similar compounds are disclosed in prior art.
  • Scope limitations: Narrow claims restrict enforcement scope, especially if competitors develop alternative compounds.
  • Patent family scope might be limited if the applicant did not expand filings internationally or across jurisdictions.

Patent Landscape Trends in China

Recent trends in Chinese pharmaceutical patent practice reveal a focus on chemical and formulation innovations with an increasing emphasis on method-of-use claims to extend patent life and coverage across indications. The Chinese patent office (CNIPA) has also demonstrated a willingness to grant patents with narrow claims if they show inventive step—particularly crucial for sophisticated chemical inventions.

Furthermore, patent linking and litigation activity around pharmaceutical patents in China have increased, emphasizing the importance of drafting comprehensive claims and clear inventive steps.


Implications for Stakeholders

  • For Innovators: CN118359585 exemplifies a strategic patent within China's fast-growing biotech sector, providing a competitive edge in the Chinese pharmaceutical market. However, maintaining broad and well-supported claims is vital for safeguarding market share.
  • For Competitors: The patent warrants thorough freedom-to-operate analyses, especially if biosimilar or alternative compounds target similar indications. Crafting non-infringing alternatives requires understanding the patent’s specific claim language.
  • For Legal Strategists: An in-depth claim construction and prior art search are essential for validity assessment, enforcement, or designing around strategies.

Conclusion

Patent CN118359585 embodies a targeted chemical and therapeutic innovation in China’s burgeoning pharmaceutical patent space. Its scope hinges on precise structural and method claims that delineate the boundaries of protection. When integrated into the wider patent landscape, it underscores the importance of strategic claim drafting and comprehensive portfolio management to maximize commercial and legal advantage.


Key Takeaways

  • The patent’s scope primarily covers specific chemical entities and their therapeutic uses, with claims crafted to delineate inventive features clearly.
  • Its enforceability depends on the uniqueness of structural features and the landscape’s prior art landscape.
  • Competitive positioning demands continuous monitoring of similar filings by domestic and international actors.
  • An integrated patent strategy enhances market leverage, especially considering China’s evolving patent examination standards.
  • Thorough prior art searches and claim interpretation are critical to assessing the patent’s strength and possible infringement risks.

FAQs

Q1: What is the primary focus of CN118359585?
A: It primarily protects a novel chemical compound, its pharmaceutical formulations, and methods of its therapeutic application.

Q2: How broad are the claims typically in Chinese pharmaceutical patents like CN118359585?
A: They may range from broad compound classes to narrow, structurally specific embodiments, depending on patent drafting and strategic objectives.

Q3: How does the patent landscape in China influence drug innovation?
A: A dynamic landscape incentivizes innovation through robust protection, though stringent examination and prior art considerations require precise claim drafting.

Q4: What are the risks associated with patent CN118359585?
A: Risks include invalidation if prior art demonstrates lack of novelty or inventive step and potential infringement risks if competitors develop similar compounds within the claim scope.

Q5: How can companies leverage this patent for commercial advantage?
A: By integrating it into a broader patent portfolio, companies can secure market exclusivity, negotiate licensing, and deter competitors in China’s pharmaceutical market.


References
[1] Chinese Patent Office (CNIPA) database.
[2] Official publication of CN118359585.
[3] Strategic patent analysis reports, China Pharmaceutical Patent Landscape 2022-2023.

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