Last Updated: May 12, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2008042973


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2008042973

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
8,642,076 Oct 3, 2027 Alnylam Pharms Inc ONPATTRO patisiran sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Key insights for pharmaceutical patentability - World Intellectual Property Organization (WIPO) patent WO2008042973

Last updated: May 12, 2026

WO2008042973 drug patent (WIPO) scope, claims, and full patent landscape analysis

WO2008042973 is a WIPO publication that is indexed as a drug-related patent application. A detailed, claim-by-claim scope analysis and an actionable landscape map (including related family members, prosecution history, claim amendments, coverage of specific indications/dosage forms/compositions, and downstream risk for generic or biosimilar entry) cannot be produced from the information provided in the prompt.

No reliable claim text, priority data, applicant/assignee, jurisdictions, or citation network can be derived without the patent document content itself. Per operating constraints, no incomplete or speculative analysis is provided.


What does WO2008042973 claim protect for the drug or composition?

Direct answer: Not provided because the claim set and specification text are not included.

Which claim types are included in WO2008042973 (composition, method of treatment, use, polymorph, salt, process)?

Direct answer: Not provided because claim categories and claim language are not included.

Does WO2008042973 claim a specific active ingredient, salt form, or pharmaceutical formulation?

Direct answer: Not provided because the active ingredient and formulation parameters are not included.

Does WO2008042973 cover dosing regimens or specific patient populations?

Direct answer: Not provided because method-of-treatment claims and dependent claim structures are not included.


How broad are the independent claims in WO2008042973 versus dependent claims?

Direct answer: Not provided because the independent claim scope and dependency structure are not included.

Claim construction indicators used in the patent (open/closed transitions, Markush groups, ranges, functional limitations)

Direct answer: Not provided because the claim wording is not included.

Scope-limiting features likely present in dependent claims

Direct answer: Not provided because dependent claim limitations are not included.


What is the patent family for WO2008042973 and what countries have related claims?

Direct answer: Not provided because family members, priority application numbers, and national/regional filings are not included.

Which jurisdictions likely mirror claim scope (EP, US, JP, CN, IN, KR)

Direct answer: Not provided because jurisdictional equivalents and status are not included.

What are the key publication and grant numbers in the family?

Direct answer: Not provided because grant/publication identifiers are not included.


How strong is the patent estate around WO2008042973 for freedom-to-operate?

Direct answer: Not provided because enforceability, claim breadth, prosecution outcomes, and expiration timelines are not included.

Are there overlapping or blocking patents citing WO2008042973

Direct answer: Not provided because the citation graph is not included.

Are there later continuation filings or improvement patents that narrow or expand scope

Direct answer: Not provided because continuation data is not included.


What other patents cite WO2008042973 and what do they claim?

Direct answer: Not provided because citation data is not included.

Forward citations by category (process, formulation, use, combination therapy)

Direct answer: Not provided because forward-citation classifications are not included.

Backward citations that may affect novelty or obviousness

Direct answer: Not provided because references listed in the application are not included.


What patents are likely involved in generic entry risk linked to WO2008042973?

Direct answer: Not provided because the drug identity, indication, and relevant regulatory product are not included.

Paragraph IV strategy risks

Direct answer: Not provided because there is no Orange Book linkage or US patent list.

Design-around feasibility based on claim structure

Direct answer: Not provided because claim language is not provided.


What is the Orange Book status of WO2008042973-related patents?

Direct answer: Not provided because the US NDA/BLA and Orange Book listing for the underlying drug are not included.

Which US patents from the family are listed for the active ingredient and dosage form

Direct answer: Not provided because patent numbers for US Orange Book listings are not provided.


What litigation or regulatory challenges involve WO2008042973 or its family members?

Direct answer: Not provided because litigation docket identifiers, parties, and case captions are not included.

Has the family been asserted in US Hatch-Waxman (district court) or ITC actions

Direct answer: Not provided because enforcement history is not included.

Settlement patterns and typical claim construction outcomes

Direct answer: Not provided because settlements and rulings are not included.


How do combination therapy claims in WO2008042973 compare with competitor patent estates?

Direct answer: Not provided because WO2008042973’s combination scope is not included.

Do the claims cover adjunct agents and co-administration regimens

Direct answer: Not provided because co-therapy claim language is not included.


What formulations or drug delivery systems does WO2008042973 cover?

Direct answer: Not provided because dosage forms and formulation parameters are not included.

Is coverage limited to tablets/capsules/suspensions or does it include sustained-release and controlled-release

Direct answer: Not provided because dosage-form examples and claims are not included.


When does WO2008042973 expire and when does exclusivity end?

Direct answer: Not provided because the filing/priority dates and jurisdiction-specific grant dates are not included.

Estimated patent term and PTA/PTG adjustments (US)

Direct answer: Not provided because US filing/grant and PTA/PTG data are not included.

PTE/PBEs and regulatory exclusivity linkage

Direct answer: Not provided because regulatory milestone data is not included.


Key Takeaways

No scope, claims, or enforceability assessment can be produced for WO2008042973 from the prompt alone. The claim set, priority and family data, and the regulatory/Orange Book and litigation linkage are not present.


FAQs

  1. What are the independent claims of WO2008042973 and what do they cover?
  2. Which family members of WO2008042973 were granted and in which jurisdictions?
  3. Are there method-of-treatment or use claims in WO2008042973 that create design-around barriers?
  4. Does WO2008042973 correspond to any Orange Book-listed patents in the US for generic litigation?
  5. What do forward citations from WO2008042973 indicate about the competitive landscape?

References

  1. (No sources cited because the WO2008042973 publication text and related records were not provided.)

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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.