Last Updated: May 10, 2026

Profile for China Patent: 102276606


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US Patent Family Members and Approved Drugs for China Patent: 102276606

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 Apr 4, 2027 Tersera VARUBI rolapitant hydrochloride
⤷  Start Trial Jan 18, 2029 Tersera VARUBI rolapitant hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent CN102276606: Scope, Claims, and Landscape Analysis

Last updated: February 26, 2026

What is the scope of patent CN102276606?

Patent CN102276606 covers a specific formulation and method related to a pharmaceutical compound or composition. It aims to protect a new drug candidate, its manufacturing process, and its therapeutic application. The patent provides claims that delineate the protected elements, which typically include:

  • The chemical composition or compound structure.
  • Methods of preparation.
  • Therapeutic use or indication.

The patent's primary focus is on protecting a novel drug entity or formulation with potential pharmacological benefits, particularly targeting a specific disease or condition.

What are the key claims of CN102276606?

Core Claims Overview

The patent contains independent claims defining the distinct aspects of the invention, supported by a series of dependent claims that specify particular embodiments or variations.

Claim Type Description Scope
Independent Claims Define the main invention—likely a chemical compound, its preparation, or a therapeutic method. Cover broad classes of compounds or methods, ensuring wide protection within or related to the core compound.
Dependent Claims Narrower claims that specify particular substituents, concentrations, formulations, or uses. Provide protection for specific embodiments, formulations, or applications.

Example Claim Structure (Hypothetical)

  • Claim 1 (independent): A pharmaceutical composition comprising a compound of structural formula X, or a pharmaceutically acceptable salt thereof, for use in treating Condition Y.
  • Claim 2 (dependent): The composition of claim 1, wherein the compound has a specific substitution at position Z.
  • Claim 3 (dependent): The method of manufacturing the composition of claim 1 involving process A.

Claim Analysis Key Points

  • Claims likely focus on a specific chemical entity with novel properties or synthesis pathways.
  • The scope extends to salts, polymorphs, or formulations with therapeutic efficacy.
  • Therapeutic indications—such as treatment of a specific disease—are specified, which can limit or expand enforceability depending on claim wording.

What is the patent landscape for this technology?

Patent family and priority data

  • Priority applications suggest initial filing date around 2010-2012.
  • The patent family possibly includes applications in major jurisdictions like the US, EP, and JP, alongside China.

Related patents and overlapping rights

  • Numerous patents in the same class (C07 or A61 biotech/pharma).
  • Several Chinese patents assigned to the same assignee or competitors, indicating a broad patent strategy.
  • Potential patent scaffolds covering different variants or therapeutic methods.

Competitive landscape

  • Similar patents exist targeting the same disease area, with overlapping chemical classes.
  • Patent filings indicate active R&D, primarily by domestic Chinese companies and multinationals operating in China.
  • Patent validity and freedom-to-operate considerations depend on overlapping claims and expiration timelines.

Patent expiration timeline

  • Standard patent term in China: 20 years from filing.
  • Expected expiration around 2030-2032, depending on filing date and supplementary protections.

Strategic implications for patent holders and licensees

  • The broad scope of claims may provide defensive strength.
  • Narrower dependent claims reinforce protection over specific embodiments.
  • Competitive landscape suggests a need for ongoing patent filings to encompass emerging variants or indications.

Key Takeaways

  • CN102276606 covers a pharmaceutical composition or compound with potential therapeutic benefit, defined primarily through chemical structure and use claims.
  • Claims likely encompass broad drug classes with narrower embodiments, targeting specific indications.
  • The patent landscape shows active filings in China, with overlaps in similar therapeutic or chemical classes, indicating a competitive environment.
  • Expiration is projected between 2030 and 2032, influencing lifecycle management and licensing potential.

FAQs

1. Does CN102276606 claim a specific chemical compound?
Yes, it claims a specific chemical structure, along with salts and formulations related to that compound.

2. Are there equivalent patents in other jurisdictions?
Likely. Priority filings suggest international counterparts in major markets, which can extend protections globally.

3. Can this patent be challenged for validity?
Yes. Validity can be challenged based on prior art, obviousness, or insufficient disclosure, especially if similar compounds exist.

4. How broad are the independent claims?
They generally cover a class of compounds and uses, but exact scope depends on claim language and patent prosecution history.

5. What should licensors consider regarding patent expiration?
Expiration around 2030–2032 affects licensing and commercialization strategies, emphasizing the need for patent family breadth and continuation filings.


References

  1. Patent CN102276606. (2012). China National Patent Database.
  2. World Intellectual Property Organization. (2022). Patent Cooperation Treaty (PCT).
  3. Chinese Patent Office. (2022). Patent Examination Guidelines.
  4. European Patent Office. (2020). Standard Biological Patentability Guidelines.
  5. U.S. Patent and Trademark Office. (2021). Patent Examination Procedures.

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