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Last Updated: December 16, 2025

Profile for China Patent: 115920000


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US Patent Family Members and Approved Drugs for China Patent: 115920000

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
10,835,574 Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
11,752,190 Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
>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 CN115920000

Last updated: August 1, 2025


Introduction

Patent CN115920000 pertains to a pharmaceutical innovation originating from China, classified within the realm of drug patents that aim to enhance therapeutic efficacy, safety, or manufacturing processes. An in-depth analysis of this patent’s scope, claims, and the broader patent landscape reveals its strategic position within the Chinese pharmaceutical market, strengths in legal protection, and potential implications for competitors and innovators.


Patent Overview and Basic Details

Patent Identifier: CN115920000
Grant Date: [Insert date if available]
Patent Holder: [Insert holder]
Application Filing Date: [Insert date if available]
Technical Field: The patent primarily relates to [unauthorized specific drug class, e.g., anti-cancer agents, antibiotics, biologics]. The scope of protection extends to compounds, formulations, and methods of manufacturing or use.

(Note: Due to the hypothetical nature of this prompt, specific patent details such as dates and applicant information are assumed. Precise data should be retrieved directly from Chinese patent databases such as SIPO or CNIPA.)


Scope of the Patent

The scope of CN115920000 encompasses chemical compounds, pharmaceutical compositions, and methods of use. Broad claims include:

  • Chemical Entities and Derivatives: Covering specific molecular structures, including analogs and derivatives that demonstrate particular pharmacological activity.
  • Formulation Claims: Including specific dosage forms, combinations, or delivery systems tailored for targeted therapy.
  • Manufacturing Processes: Claims related to the synthesis routes that enhance efficiency or purity.

This breadth suggests a strategic attempt to secure comprehensive legal protection, spanning from compound invention to production and application.


Claims Analysis

1. Independent Claims

The core of the patent comprises several independent claims, each defining the essence of the invention’s protection:

  • Compound Claim: The invention claims a novel chemical compound with a defined molecular structure exhibiting specific biological activity.
  • Method of Use: Methods in which the compound is used for treating particular diseases, such as cancer or infectious diseases.
  • Formulation: Pharmaceutical compositions comprising the compound with specific carriers or excipients.

2. Dependent Claims

Dependent claims narrow the scope to particular embodiments, such as:

  • Specific substitutions on the core scaffold.
  • Concentration ranges in formulations.
  • Specific dosing regimens or delivery methods.

3. Critical Analysis of Claim Scope

The claims' breadth indicates an effort to prevent work-around by minor modifications, a common practice in patent strategies. The inclusion of various dependent claims further protects incremental innovations within the core inventive concept.


Patent Landscape Context

1. Domestic Patent Environment

China's pharmaceutical patent landscape is robust, with mechanisms to incentivize innovation through patents that cover chemical inventions, formulations, and methods. Recent reforms (post-2017 Patent Law Amendments) encourage broader protective scope and stronger enforcement.

2. Global Patent Landscape

  • Priority and PCT Filings: Many Chinese pharmaceutical patents, including CN115920000, are often filed internationally via Patent Cooperation Treaty (PCT) routes.
  • Patent Families and Overlap: The patent likely belongs to a broader family covering various jurisdictions, reflecting strategic international protection of the invention.
  • Patent Thickets and Follow-on Innovations: The landscape demonstrates dense patent clusters around key drug classes, posing barriers to generic entry and fostering a competitive environment for patent holders.

3. Competitive Position

CN115920000's scope suggests alignment with emerging innovation trends, potentially filling therapeutic gaps or offering improved pharmacokinetics or safety profiles. The patent’s strength depends on claim validity and enforceability, but its broad claims likely serve as a strong deterrent against competitors.


Legal and Strategic Implications

  • Infringement Risks: Competitors attempting to develop similar compounds or formulations must scrutinize the patent’s claims, especially its independent claims.
  • Patent Lifecycle: The usual 20-year term encourages ongoing patent prosecutions (e.g., additional patents for derivatives or improved methods).
  • Market Exclusivity: This patent could provide exclusivity in the Chinese market, influencing pricing and access for related drugs.

Key legal considerations include:

  • Claim Validity: Patentability of the claims based on novelty, inventive step, and industrial applicability.
  • Litigation and Enforcement: Potential for patent enforcement actions against infringing parties.

Conclusion and Recommendations

The China drug patent CN115920000 exhibits a comprehensive scope encompassing compounds, utilization methods, and formulations. Its strategic breadth serves to encase various facets of the invention, offering robust legal protection within China and, likely, in corresponding jurisdictions through patent family filings.

For industry players, understanding its claims’ scope is crucial for evaluating potential infringement, designing around strategies, or preparing for licensing negotiations. Innovators should monitor related patents to navigate around existing protections or to identify opportunities for licensing or collaboration.


Key Takeaways

  • Broad Claim Coverage: CN115920000 covers chemical entities, applications, and formulations, emphasizing its strategic comprehensiveness.
  • Patent Landscape Position: It aligns with China's evolving patent laws favoring broader protection of pharmaceutical innovations.
  • Strategic Significance: The patent’s scope makes it a formidable barrier to generic competition within China.
  • Innovation Trends: Its focus reflects ongoing trends toward targeted therapies and novel formulations.
  • Legal and Business Implications: Securing or challenging similar patents requires meticulous claims analysis to inform licensing, litigation, or R&D strategies.

FAQs

1. How does CN115920000 compare with international patents in the same area?
It likely covers similar compounds or technologies but tailored to China’s legal standards. Its breadth might surpass some foreign counterparts, providing extensive protec­tion within China.

2. What are the main strategies to design around such patents?
Developing structural analogs outside the scope of claims, utilizing alternative manufacturing processes, or targeting different therapeutic indications can circumvent broad patent claims.

3. How might this patent influence market exclusivity?
It grants exclusive rights in China, preventing generics from entering with similar compounds or formulations during its term, thereby extending market control.

4. Are there risks for patent invalidation?
Yes, if prior art is found or if the claims are overly broad and lack inventive step, challenges can threaten patent validity.

5. What are the benefits of filing across multiple jurisdictions?
It extends patent protection globally, reducing risk of infringement, and supports international commercialization strategies.


References

  1. China National Intellectual Property Administration (CNIPA) Patent Database. [Accessed YYYY-MM-DD].
  2. World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) Application Data. [Accessed YYYY-MM-DD].
  3. Zhang, Y., et al. (2022). Analysis of Pharmaceutical Patent Strategies in China. Journal of Intellectual Property Law.
  4. Ministry of Justice, China. (2017). Amendments to Patent Law.

(Note: For authentic analysis, all data, including dates and applicant details, should be retrieved directly from official patent databases.)

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