Last Updated: May 12, 2026

Profile for Eurasian Patent Organization Patent: 202092118


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 202092118

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
10,240,152 Oct 20, 2029 Alnylam Pharms Inc ONPATTRO patisiran sodium
8,168,775 Aug 10, 2032 Alnylam Pharms Inc ONPATTRO patisiran sodium
8,741,866 Oct 20, 2029 Alnylam Pharms Inc ONPATTRO patisiran sodium
9,234,196 Oct 20, 2029 Alnylam Pharms Inc ONPATTRO patisiran sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Key insights for pharmaceutical patentability - Eurasian Patent Organization patent EA202092118

Last updated: April 23, 2026

What does Eurasian Patent Organization application EA202092118 claim, and what is its likely drug-patent scope?

Scope and claim set for EA202092118

No complete, citable claim text or full bibliographic record for EA202092118 is present in the information available in this chat. Without the application’s published document, claim numbering, and any granted/refused status text, a claim-by-claim scope map cannot be produced without risking inaccuracies.

Is EA202092118 a drug patent with enforceable pharmaceutical coverage?

EA202092118 cannot be verified from the available inputs as:

  • a granted Eurasian patent versus a pending application,
  • a formulation, polymorph, method-of-treatment, method-of-manufacture, or use patent, or
  • a composition-of-matter versus process- or use-limited claim set.

Because these elements determine enforceable claim scope, any landscape characterization would be speculative.

Patent landscape: what sits around EA202092118

A defensible landscape requires at minimum:

  • the applicant/assignee,
  • the title/IPC/CPC,
  • publication numbers (EA publication, PCT/WO, EP, RU, KZ, etc.),
  • priority data,
  • the claim categories and key dependent claim limitations, and
  • prosecution outcomes in Eurasia and parallel jurisdictions.

None of these identifiers are available here. As a result, no authoritative mapping to related family members, epitomes, obviousness clusters, or freedom-to-operate-relevant risks can be delivered.

What can be concluded from EA202092118 alone

Given the absence of any accessible EA publication data, the only accurate conclusion is that EA202092118 cannot be analyzed in terms of claim scope and surrounding landscape from the material provided.


Key Takeaways

  • EA202092118’s claim scope and enforceability cannot be determined from available inputs in this chat.
  • A non-speculative patent landscape requires the publication record and claim text; those are not provided.

FAQs

  1. Can EA202092118 be analyzed claim-by-claim without its published claim set?
    No. Claim scope depends on the exact wording and numbering of the published claims.

  2. Can a drug-patent landscape be built without identifying the family and priority data?
    No. Landscape analysis requires publication identifiers across jurisdictions to find overlapping or adjacent rights.

  3. Does “EA202092118” alone reveal the patent type (composition, method, use)?
    No. Patent type is not inferable from the identifier alone.

  4. Is it possible to determine enforceable scope without knowing grant status?
    No. Pending and granted claims can differ materially, and Eurasian enforcement tracks the granted text.

  5. Can this analysis be completed by referencing generic Eurasian practice?
    No. Specific claim scope and landscape impact must be tied to the actual EA document content.


References

[1] None provided in the available material for EA202092118.

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.