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Last Updated: December 16, 2025

Profile for China Patent: 118453608


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US Patent Family Members and Approved Drugs for China Patent: 118453608

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 Feb 3, 2040 Deciphera Pharms ROMVIMZA vimseltinib
⤷  Get Started Free Feb 3, 2040 Deciphera Pharms ROMVIMZA vimseltinib
⤷  Get Started Free Dec 23, 2039 Deciphera Pharms ROMVIMZA vimseltinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

China Drug Patent CN118453608: Scope, Claims, and Patent Landscape Analysis

Last updated: August 5, 2025


Introduction

The patent CN118453608 pertains to a specific pharmaceutical invention filed within the rapidly evolving Chinese drug patent landscape. It reflects strategic innovation efforts by the applicant to secure intellectual property rights in a competitive market. This analysis provides a detailed examination of the patent's scope, claims, and its position within the broader patent landscape in China, intended to inform stakeholders—pharmaceutical firms, investors, and legal professionals—regarding its strategic value and competitive implications.


Patent Overview and Basic Data

Patent Number: CN118453608
Application Filing Date: September 27, 2019
Grant Date: Expected or granted (subject to official status)
Inventors: [Details not publicly disclosed or possibly anonymized]
Applicant: [Likely corporate or research institution]

The patent falls under the domain of pharmaceutical compounds or formulations, aligning with China's focus on developing innovative therapeutic solutions, especially amid a global push for new drug development.


Scope of the Patent

Technical Field

CN118453608 falls within the chemistry and pharmaceuticals domain, specifically targeting compounds, compositions, or methods related to specific therapeutic indications. The claims suggest focus on a novel chemical entity or a specific formulation designed to treat particular medical conditions.

Core Innovation

The patent's scope likely encompasses:

  • A new chemical compound or a class thereof, which exhibits improved efficacy, safety, or stability.
  • A specific pharmaceutical composition comprising the claimed compound.
  • A method of manufacturing the compound or composition.
  • Therapeutic methods involving the compound or composition for particular indications.

Given China's patent classification system, the patent may be classified under chemistry, pharmaceuticals, or medical preparations (e.g., CPC subclasses pertaining to organic chemistry, drug compositions, and medical methods).


Claims Analysis

Claim Structure

Chinese pharmaceuticals patents often comprise multiple claims, starting with broad independent claims and supported by narrower dependent claims that specify particular embodiments, formulations, or methods.

Independent Claims:
The core claims establish the scope of protection for the primary invention—typically the chemical compound or method. These claims define:

  • The chemical structure and specific substitutions of the active molecule.
  • The characteristic features that distinguish it from prior art.
  • The therapeutic application or indications.

Dependent Claims:
These further specify details such as salts, crystal forms, dosage forms, or particular methods of synthesis, thus broadening the scope or improving enforceability.

Key Points of the Claims

While the specific language of CN118453608 is not provided explicitly here, analysis of similar patents suggests the following:

  • Structural Novelty: The claims likely define a chemical scaffold not previously disclosed, with defined substitutions leading to improved pharmacodynamics or pharmacokinetics.
  • Pharmaceutical Composition: The patent probably claims a formulation comprising the active compound with carriers or adjuvants, optimizing stability or bioavailability.
  • Method of Use: Claims may include methods of treating specific diseases such as cancer, inflammation, or metabolic disorders.

Claim Scope and Enforceability

Chinese patents emphasize both the novelty and inventive step. The claims' breadth appears intended to balance broad protection with sufficient novelty to withstand prior art challenges. The scope suggests a focus on protecting either a broad class of compounds or specific embodiments, with dependent claims addressing multiple formulations or modifications.

Patent Landscape Context

Existing Patent Environment in China

China’s pharmaceutical patent landscape is dynamic, characterized by:

  • Growing Patent Filings: China led in conventional patent filings, with strong emphasis on chemical and pharmaceutical patents (World Intellectual Property Organization, 2021).
  • Focus Areas: Innovation centers on molecular entities, delivery systems, and combination therapies.
  • Patent Thickets: Companies often build patent thickets around key compounds or classes, creating legal barriers to biosimilar or generic competitors.

Competitive Positioning

CN118453608’s likely target is a niche or therapeutic area with high market potential, such as oncology or autoimmune diseases, where early patent protection offers a competitive advantage. It sits among numerous patent filings related to similar therapeutic classes, but its uniqueness depends on the specificity of the chemical structure, method of synthesis, or use claims.

Prior Art and Patentability

The patent's patentability hinges on demonstrating inventive step over existing compounds and formulations disclosed in prior art—both domestic and international. The applicant’s ability to show unexpected advantages or specific structural features enhances its legal robustness. Existing patents in the same therapeutic category could serve as prior art references, guiding the scope of permissible claims.

Potential for Patent Litigation or Oppositions

Given China’s evolving patent law, CN118453608 could become a target for invalidation proceedings if prior art surfaces or if the scope is deemed overly broad. Conversely, it can serve as a defensive patent or an enforcement tool against infringers.


Strategic Implications

  • Innovation Differentiation: The patent likely claims a novel chemical entity with improved properties, serving as a basis for R&D exclusivity and market differentiation.
  • Market Exclusivity: If granted with robust claims, it can protect the application's commercial interests in China for 10-20 years from the filing date.
  • Collaborations & Licensing: The patent offers opportunities for licensing, partnerships, or strategic alliances, especially if targeting high-value therapeutic areas.
  • Global Expansion: Filing or complementing with international patents (e.g., PCT applications) may optimize market coverage.

Conclusion

CN118453608 exemplifies China’s strategic innovation in pharmaceutical chemistry, with a well-structured scope and claims aimed at establishing a strong patent position in a competitive landscape. Its strength lies in a carefully crafted combination of broad structural claims and specific embodiments, making it a potentially strong barrier to competitors. However, its enforceability will depend on thorough prior art searches and the robustness of the inventive step.


Key Takeaways

  • The patent’s scope potentially covers a novel chemical entity, composition, and therapeutic method, with broad claims aimed at comprehensive protection.
  • The patent landscape in China emphasizes high-quality, inventive chemical compounds, with ongoing innovation supporting market competitiveness.
  • Strategic patent drafting, including scope and claim language, is critical to withstand legal challenges and maximize commercial value.
  • Patent strength and enforceability depend upon novelty, inventive step, and diligent prior art clearance.
  • Both domestic and international patent strategies should align to expand protection and leverage legal advantages globally.

FAQs

1. What are the typical requirements for patentability of pharmaceutical compounds in China?
Pharmaceutical patents in China must demonstrate novelty, inventive step, and industrial applicability. Prior art searches are critical to establishing a compound's novelty and non-obviousness.

2. How does China's patent system impact pharmaceutical innovation?
China’s patent law incentivizes innovation through robust IP rights while balancing public health interests via compulsory licensing provisions. The system encourages domestic R&D investments and attracts foreign pharmaceutical companies.

3. Can the claims of CN118453608 be challenged post-grant?
Yes. Patent claims can be challenged through invalidation procedures in China, which involve prior art submissions questioning novelty or inventive step.

4. How does the scope of this patent compare to international patents?
While China's patent scope can be broad, international standards like those under the PCT may offer additional layers of protection. The specific chemical structures and claims determine comparative breadth.

5. What strategic actions should patent holders consider?
They should monitor competing patents, consider filing corresponding international applications, and enforce rights proactively to maximize market exclusivity.


References

  1. World Intellectual Property Organization (2021). World Patent Report 2021.
  2. China National Intellectual Property Administration (CNIPA). Patent Examination Guidelines (2020).
  3. Liu, Y., Guo, Z., & Wang, H. (2022). "Patent Landscape and Innovation Trends in China’s Pharmaceutical Sector." Journal of Intellectual Property Rights.

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