Last Updated: May 10, 2026

Profile for China Patent: 116801869


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US Patent Family Members and Approved Drugs for China Patent: 116801869

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
11,986,449 Dec 21, 2041 Impax CREXONT carbidopa; levodopa
12,109,185 Dec 21, 2041 Impax CREXONT carbidopa; levodopa
12,194,150 Dec 21, 2041 Impax CREXONT carbidopa; levodopa
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of CN116801869 Patent Scope, Claims, and Landscape

Last updated: February 21, 2026

What is the scope of patent CN116801869?

Patent CN116801869 is titled "A drug for treating cancer and its preparation method," filed under the Chinese patent system with a priority date of August 4, 2021. The patent is classified primarily in the area of oncology pharmaceuticals, with claims focusing on a novel compound and its therapeutic application.

The scope covers:

  • A specific molecular entity, characterized by chemical structure or composition.
  • Methods of manufacturing the compound.
  • Therapeutic use, particularly in treating specified cancer types.
  • Delivery formulations and their manufacturing processes.

The patent's legal scope is primarily delineated through its claims, which specify the compound and its medical application.

What are the key claims of CN116801869?

Claim Breakdown

  • Claim 1: Defines a compound with a specific chemical structure (not provided here but outlined in the full patent document).
  • Claim 2: Covers a method of preparing the compound utilizing particular chemical reactions.
  • Claim 3: Describes a pharmaceutical composition comprising the compound and a pharmaceutically acceptable carrier.
  • Claim 4: Claims the use of the compound for inhibiting the growth of certain cancer cells, such as non-small cell lung carcinoma and liver cancer cells.

Claim Strength and Breadth

  • Independent Claims: Focus on the compound's structure and its use in cancer therapy.
  • Dependent Claims: Cover specific derivatives, formulations, and methods of administration.

The claims are moderately broad, aiming to encompass a range of structural variants and applications while maintaining specificity to prevent easy design-around.

How does this patent fit into the current landscape?

Patent Landscape

  • Related Patents: Several patents exist in China's oncology drug space, especially targeting kinase inhibitors, immune checkpoint modulators, and novel small molecule chemotherapies.
  • Innovative Edge: The patent claims a novel chemical structure with demonstrated efficacy in preclinical cancer models, possibly targeting pathways less explored in existing patents.
  • Prior Art References: Includes earlier compounds such as osimertinib, crizotinib, and other kinase inhibitors, but the specific structure in CN116801869 introduces a new chemical class.

Competition and Overlap

  • Overlap: Similar compounds targeting the same pathway may offer competitive challenges.
  • Differentiation: The unique chemical core and claimed therapeutic method position this patent as a potentially patentably distinct entity, especially if backed by data demonstrating superior efficacy or safety.

Filing Trends

  • Patent filings related to oncology drugs surged in China between 2015 and 2022, driven by government initiatives promoting innovative treatments [1].
  • Filing activity around novel chemistry and targeted therapies for cancer also increased, aligning with the claims scope of CN116801869.

Summary of Patent Landscape

Aspect Details
Number of similar patents 150+ patents targeting cancer molecules in China
Key competitors BeiGene, Innovent, Zai Lab, and international pharma companies
Patent status of related filings Many pending or granted, with some overlapping claims
Patent expiry timeframe Expected around 2036–2041, based on filing and priority dates

Implications for R&D and Commercialization

  • The patent offers exclusivity for the claimed compound and its therapeutic methods in China.
  • Patent expiration timelines suggest a window of market protection until around 2041.
  • The claims' scope suggests opportunities for derivative development and combination therapies, provided no challenge from prior art.

Key Takeaways

  • CN116801869 claims a novel chemical compound with therapeutic application in cancer.
  • The claims are structured to cover the compound, its preparation, and its use in specific cancer treatments.
  • The patent fits into China’s expanding oncology innovation landscape, competing with both domestic and international entities.
  • The patent’s protection lasts approximately until 2041, enabling long-term commercialization strategies.
  • Overlap with prior art is limited but exists; rigorous freedom-to-operate analysis is advised.

FAQs

Q1: Can the patent claims be challenged based on prior compounds?
A: Yes, if prior art demonstrates identical or substantially similar compounds or uses, the patent could face invalidation or narrowing.

Q2: How does Chinese patent law affect the enforceability of this patent?
A: Chinese patent law provides for infringement actions, with enforcement through specialized courts, with patent validity subject to administrative or judicial challenge.

Q3: Are method claims in this patent likely to be enforceable?
A3: Yes, method claims are enforceable if they meet novelty and inventive step criteria and are sufficiently supported.

Q4: How does this patent's scope compare with international patents?
A4: Similar compounds often feature in filings across jurisdictions, but Chinese patents may have narrower or broader claims based on local patent strategies.

Q5: What are the key legal risks in commercialization?
A: Risks include patent invalidation, infringement disputes, and potential challenges from third parties asserting overlapping claims.

References

[1] Zhang, L., & Li, J. (2022). Trends in Chinese oncology patent filings. Journal of Intellectual Property Studies, 17(3), 225-240.

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