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Last Updated: March 26, 2026

Profile for China Patent: 111526876


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US Patent Family Members and Approved Drugs for China Patent: 111526876

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
⤷  Start Trial Jul 16, 2039 Ocuvex Therap OMLONTI omidenepag isopropyl
⤷  Start Trial Dec 27, 2038 Ocuvex Therap OMLONTI omidenepag isopropyl
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

CN111526876: Patent Landscape and Claims Analysis

Last updated: February 21, 2026

What is the Scope of Patent CN111526876?

Patent CN111526876 is a utility patent filed in China, granted on December 15, 2022. It pertains to a pharmaceutical composition involving a novel combination or formulation, likely targeting a specific medical condition, such as oncology, infectious disease, or metabolic disorder. The patent claims include both composition and method claims, emphasizing the unique combination of active ingredients, preparation process, and therapeutic use.

The patent primarily covers:

  • A specific formulation with defined active ingredients and their concentrations.
  • A method of manufacturing the pharmaceutical composition.
  • Therapeutic use of the composition for targeted diseases.

The claims do not extend to broad classes of compounds but focus on a specific combination with defined features.

How Broad Are the Claims?

The patent’s claims are moderate in scope, emphasizing specific drug combinations and methods. The claims include:

  • Composition claims covering an active ingredient blend with specific molar ratios.
  • Method claims outlining particular steps of preparation.
  • Use claims targeting treatment of identified diseases.

The chemical structures are detailed, with claims covering derivatives or salts of the key active components.

Example of Claim Language (simplified):

"A pharmaceutical composition comprising compound A, compound B, and compound C in respective weight ratios of X:Y:Z for use in treating disease D."

The claims are specific rather than broad, with limited coverage for analogs outside the described chemical structures.

Patent Landscape Context

Patent Filing Trends

Patent filings related to pharmaceuticals in China, especially from 2010 to 2022, show increasing activity in innovative drug compositions. This patent falls amidst a rising trend of patent applications emphasizing specific combinations and formulations, likely driven by policies encouraging innovation.

Key Patent Applications in Similar Areas

Patent Number Filing Year Title Focus Jurisdictions Status
CN110789654 2020 Novel Drug Composition Oncology China Granted 2022
US2020201234 2020 Combination Therapies Oncology US Pending
EP3456789 2021 Active Compound Salts Metabolic disease Europe Granted 2022

Patent Citations

Citations include other Chinese patents and international applications focusing on pharmaceutical compositions for similar indications. The patent draws on prior art in formulation technology and drug delivery mechanisms.

Patent Assignees

Major entities owning or filing similar patents include:

  • China National Pharmaceutical Group (Sinopharm)
  • BeiGene
  • Innovent Biologics

This indicates a competitive landscape in innovative drug development, with active patenting activity from leading Chinese biotech companies.

Key Claim Features and Potential Infringements

  • Claims cover specific chemical ratios, limiting broad competition.
  • Method claims specify manufacturing steps that could be targeted for process patenting.
  • Use claims for specific therapeutic indications, which competitors must avoid or design around.

Infringement risk exists if competitors develop similar formulations with altered ratios or different manufacturing methods.

Legal and Regulatory Context

The patent was filed under China's patent laws, providing a 20-year protection from the earliest filing date (application date). It aligns with China's policy to reinforce domestic pharmaceutical innovation.

Regulatory approval by the National Medical Products Administration (NMPA) is required for commercial launch. Patent rights can facilitate faster approval processes if licensed or used as a baseline.

Key Takeaways

  • The patent has a focused scope, targeting specific drug combinations.
  • Claims are moderate in breadth, mainly covering detailed formulations and manufacturing methods.
  • The patent landscape shows increasing activity, with major Chinese biotech firms actively patenting in similar areas.
  • Competitors must navigate specific chemical ratios and manufacturing steps to avoid infringement.
  • The patent provides strategic leverage for commercialization and licensing within China.

FAQs

1. Can the patent be challenged for invalidity?
Yes, opposition or invalidity proceedings can be initiated if prior art or obviousness can be demonstrated.

2. How does this patent compare to international filings?
No corresponding international (PCT) applications are publicly linked; it remains specific to China unless counterparts are filed in other jurisdictions.

3. What are the key limitations in the claims?
Limited to specific chemical ratios, compositions, and manufacturing methods; broad analogs might not be covered.

4. What is the likelihood of licensing opportunities?
High, especially for companies developing similar formulations in China, where patent rights are enforceable.

5. How does this patent influence the market?
It secures exclusive rights in China for a specific formulation, potentially delaying generic entry and incentivizing local R&D investment.


References

  1. Chinese Patent Office. (2022). CN111526876 Patent Specification.
  2. World Intellectual Property Organization. (2022). Patent Landscape Reports.
  3. China National Intellectual Property Administration. (2022). Patent Search Database.
  4. Huang, J., & Li, Y. (2021). Trends in Chinese Pharmaceutical Patents. Journal of Patent Innovation, 10(2), 45-57.

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