Last Updated: May 11, 2026

Profile for China Patent: 101420854


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for China Patent: 101420854

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
8,168,614 Jul 20, 2030 Anacor Pharms Inc EUCRISA crisaborole
8,501,712 Aug 16, 2027 Anacor Pharms Inc EUCRISA crisaborole
9,682,092 Aug 16, 2027 Anacor Pharms Inc EUCRISA crisaborole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Key insights for pharmaceutical patentability - China patent CN101420854

Last updated: April 23, 2026

What Does CN101420854 Cover, and How Broad Are Its Claims in China’s Patent Landscape?

CN101420854 is a Chinese patent publication that discloses a specific pharmaceutical composition and/or method claim set (as typically drafted for China drug patents). Without the claim text and bibliographic details (applicant, title, publication dates, and claim list), a complete and accurate scope-and-claims analysis and a landscape mapping of related filings cannot be produced to a standard suitable for decision-making.

CN101420854 cannot be analyzed in full scope and claim detail from the information provided in this prompt. The request requires exact claim language, claim dependencies, defined terms, and cited prior art/related family members. Those elements are not present here, so any attempt to fill gaps would risk factual errors.


What Claims Exist in CN101420854?

A claim-by-claim scope analysis requires the patent’s exact claim set, including:

  • independent claim(s) (composition, dosage form, method of treatment, manufacturing method, or use claims)
  • dependent claims (active ingredient specificity, excipient lists, process steps, particle size, stability parameters, polymorph form, route restrictions)
  • any Markush language, ranges (e.g., concentration, pH, temperature, time), and defined ranges
  • whether the claims are product, process, or Swiss-type/use format
  • claim numbering and whether there are claim amendments across publication/grant

This cannot be extracted from the prompt.


What Is the Patent Scope in Practical Commercial Terms?

To translate CN101420854 scope into actionable commercial impact, the analysis must map:

  • which active pharmaceutical ingredients (APIs) are covered
  • whether the claims cover:
    • the API per se
    • a salt/solvate/polymorph of the API
    • a formulation with specific excipients
    • a dosing regimen (dose, frequency, duration)
    • a method of manufacture with defined parameters
  • the level of claim specificity (broad genus vs narrow embodiment)
  • whether design-around exists via:
    • alternative salts/polymorphs
    • alternate excipient systems
    • alternate processes

None of the above is available from the prompt.


How Does CN101420854 Fit the Wider China Drug Patent Landscape?

A landscape requires at minimum:

  1. Family linkage

    • priority date(s)
    • PCT/overseas filing equivalents
    • continuation/divisional equivalents (if any)
  2. China prosecution status

    • whether CN101420854 is granted or lapsed
    • term adjustments and current legal status
    • effective term end date in China (for enforcement window)
  3. Forward and backward citation network

    • cited documents in the patent
    • later publications that reference the same technical core
  4. Competitor and generic exposure

    • likely generic development targets
    • whether later filings attempt to carve out claim features

These elements require access to the patent record and claim text.


What Enforcement-Relevant Features Must Be Checked?

For China drug patents, enforcement hinges on claim construction and evidence. The scope analysis typically checks:

  • product claim elements: ingredient identity, form, and formulation parameters
  • method claim elements: step order, conditions, and process parameters
  • infringement proof: composition analysis, manufacturing records, and test data
  • validity risk: obviousness-type reasoning under CN practice, enablement, and support for broad ranges
  • whether the claims are susceptible to narrowing during prosecution or in reexamination

Again, the content of CN101420854 is not available here.


What Can Be Done Reliably With the Provided Information?

Nothing actionable can be stated about scope and claims, because the prompt does not include:

  • patent title
  • abstract
  • full claim text
  • applicant/assignee
  • publication dates and grant status
  • independent/dependent claim structure
  • cited art and related documents

Under the requirement for “complete and accurate response,” that missing record prevents a correct analysis.


Key Takeaways

  • CN101420854’s scope and claims cannot be analyzed from the prompt alone.
  • A valid landscape assessment requires the patent’s bibliographic record, exact claim language, and legal status details.
  • Any attempt to describe coverage or claim breadth without the claim set would not meet the accuracy standard required for patent and litigation decision-making.

FAQs

1) Can CN101420854 be assessed for claim breadth without the exact claim text?
No. Claim breadth depends on the precise independent and dependent claim language, ranges, and defined terms.

2) Does a Chinese publication number alone identify the drug product or composition covered?
No. Bibliographic and claim-level data are required to map the patent to an API, formulation, or method.

3) Can the patent landscape be mapped without family and status data?
No. Landscape work requires priority and family members, prosecution and grant status, and citation networks.

4) What matters most for infringement in China drug patents?
The claim elements (including formulation or process conditions) and the ability to prove those elements in the accused product or process.

5) What is typically the fastest path to a usable landscape for a CN drug patent?
Extract title, abstract, and full claim set, then pull legal status, family equivalents, citations, and later competing filings.


References (APA)

[1] No sources were provided or retrievable from the prompt content.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.