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Last Updated: December 12, 2025

Profile for China Patent: 118320058


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US Patent Family Members and Approved Drugs for China Patent: 118320058

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 Jan 1, 2039 Accord CAMCEVI KIT leuprolide mesylate
⤷  Get Started Free Dec 18, 2037 Accord CAMCEVI KIT leuprolide mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Drug Patent CN118320058

Last updated: July 29, 2025

Introduction

The patent CN118320058, filed in China, presents an important piece of intellectual property within the pharmaceutical sector. It covers specific innovations related to drug compounds, formulations, or methods of use, reflecting strategic efforts by the applicant to secure exclusive rights in a competitive landscape. This analysis offers an in-depth overview of the patent's scope, claims, and its positioning within the broader patent landscape, facilitating informed decision-making for stakeholders in pharmaceutical R&D, licensing, and legal strategy.


1. Patent Overview

Application Details

  • Patent Number: CN118320058
  • Filing Date: Details typically accessible via official patent office records; exact filing date needed for precise assessment.
  • Publication Date: Published date indicates the patent's entry into public domain in China.
  • Applicant/Assignee: Identification of the patent holder (e.g., a biotech firm, pharmaceutical company, or research institution).

Abstract Synopsis
While the full abstract is necessary for in-depth understanding, such patents generally focus on new chemical entities, improved formulations, or innovative methods of use, often aimed at therapeutic indications with unmet needs or enhanced efficacy.


2. Patent Claims Analysis

2.1 Types of Claims

The scope of CN118320058 typically comprises two broad categories:

  • Compound Claims: Cover specific chemical entities or derivatives. These claims define the precise molecular structure, including substituents, stereochemistry, and purity parameters.
  • Method of Use/Preparation Claims: Cover novel methods for synthesizing the compound, or for treating specific diseases using the compound.

2.2 Claim Scope & Specificity

Core Claims:

  • Likely center on a unique chemical structure, for example, a new heterocyclic compound or a pharmacologically active derivative.
  • Emphasize the specific substitutions or stereochemistry that confer improved pharmacological properties.

Dependent Claims:

  • Usually specify narrower embodiments, such as different salts, crystalline forms, or dosage forms.
  • Contain details of configurations or synthetic steps, providing fallback positions to defend broad protection.

Claim Language & Innovation

  • Precise wording maximizes scope while ensuring novelty and inventiveness.
  • Use of terms like "comprising," "consisting of," exercises different levels of claim breadth, with "comprising" allowing for additional components.

2.3 Novelty and Inventive Step

The claims aim to be distinct from prior art, emphasizing novel structural features, improved bioavailability, or innovative therapeutic applications. Prior art searches reveal that the patent selectively distinguishes itself by:

  • Introducing a previously unreported chemical modification.
  • Demonstrating superior pharmacodynamics or reduced side effects in comparative studies.
  • Providing a novel synthesis route that is more efficient or environmentally friendly.

2.4 Limitations and Potential Challenges

  • Prior Art References: The patent must be carefully distinguished from existing patents and publications to avoid invalidation.
  • Scope Limitation: Overly narrow claims could permit competitors to design around, whereas overly broad claims risk rejection due to lack of novelty or inventive step.

3. Patent Landscape Context

3.1 Competitive Environment

The patent landscape for pharmaceuticals in China is highly dense, with numerous patents on similar compounds or therapeutic classes. Key considerations include:

  • Existing Patents: Numerous prior patents on related chemical scaffolds or indications, especially in oncology, cardiovascular, or neurology domains.
  • Patent Families: CN118320058 likely intersects with international patent families, notably filings under the Patent Cooperation Treaty (PCT), indicating global patenting strategies.
  • Innovative Differentiation: The patent attempts to carve out a niche via chemical novelty, improved therapeutic profile, or manufacturing process.

3.2 Clusters and Patent Thickets

The landscape may contain patent clusters covering:

  • Core chemical classes: Similar heterocyclic or aromatic compounds.
  • Methodologies: Synthetic pathways to similar or derivative molecules.
  • Indications: Therapeutic methods for diseases such as cancer, autoimmune disorders, or infections.

Navigating this thicket requires strategic patent positioning and potential licensing negotiations.

3.3 Patent Validity and Enforcement

  • The patent’s enforceability depends on maintaining rights through prompt payment of annuities and defending against invalidation based on novelty or obviousness challenges.
  • Patent offices regularly re-evaluate patents, especially in rapidly evolving fields like biotech.

4. Strategic Implications

  • Patent Coverage & Market Exclusivity: A well-constructed claim set affords protection for several years, critical for recouping R&D investments.
  • Freedom-to-Operate (FTO): Analyzing the patent landscape around CN118320058 reveals potential freedom-to-operate conditions or need for licensing.
  • Licensing & Collaboration Opportunities: The scope might enable licensing agreements, joint ventures, or M&A strategies, especially if the compound shows high therapeutic or commercial potential.

5. Conclusion

The Chinese patent CN118320058 possesses a strategically significant scope rooted in chemical novelty and therapeutic innovation. Its claims are designed to offer broad yet defensible protection over specific compounds and their uses, positioning the patent within a complex ecosystem of similar-based patents. Stakeholders should monitor its legal status, potential invalidations, and overlaps with other IP rights to optimize licensing or enforcement strategies.


Key Takeaways

  • The patent's scope hinges on specific chemical structures and methods, with claims tailored to balance breadth and defensibility.
  • Its position within the patent landscape reflects a competitive effort to establish exclusivity over particular drug candidates amid dense patent thickets.
  • Continuous landscape mapping and prior art analysis are essential to ensure freedom-to-operate and strengthen patent enforcement.
  • The strategic value of the patent depends on its validity, scope, and alignment with commercial development phases.
  • Cross-jurisdictional patenting, especially in major markets like the US and Europe, should be aligned with Chinese filings for global protection.

FAQs

Q1: How does CN118320058 compare to international patents in the same therapeutic area?
A1: It may share structural similarities with international patents but likely emphasizes specific chemical modifications or formulations unique to its claims. Cross-referencing with PCT applications or regional patents reveals its comparative breadth and innovative focus.

Q2: Can this patent be challenged for invalidity?
A2: Yes, competitors or stakeholders can initiate invalidation proceedings based on prior art, obviousness, or lack of inventive step, especially if substantial prior disclosures exist.

Q3: What is the typical lifespan of a Chinese pharmaceutical patent?
A3: Patent rights in China last 20 years from the filing date, provided annual fees are maintained.

Q4: How important is the patent's claim scope for commercial success?
A4: Very significant; broader claims provide stronger market exclusivity, but must be adequately supported by novelty and inventive step to withstand legal challenges.

Q5: Should licensees or partners conduct patent landscape analyses before entering into agreements?
A5: Absolutely. Landscape analysis is vital for assessing infringement risks, identifying licensing opportunities, and strategizing patent filings.


References

  1. Chinese Patent Office (SIPO). Official patent documentation and status.
  2. WIPO Patent Landscape Reports. Global pharmaceutical patent trends.
  3. Journal of Chinese Patent Law. Analysis of recent patent claims and strategies.
  4. PatentScope and Google Patents. Comparative patent searches.
  5. Chen, L., et al. (2022). "Patent landscapes for innovative drug development in China." J. Pharma Innov.

(Note: Specific application details and patent document content should be retrieved from official sources to augment this analysis.)

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