You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: March 26, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2011002817


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2011002817

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 Feb 24, 2031 Agios Pharms Inc AQVESME mitapivat sulfate
⤷  Start Trial Feb 24, 2031 Agios Pharms Inc PYRUKYND mitapivat sulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

WIPO Patent WO2011002817: Scope, Claims, and Patent Landscape

Last updated: February 27, 2026

What is the scope of WO2011002817?

WO2011002817 is a World Intellectual Property Organization (WIPO) international patent application filed under the Patent Cooperation Treaty (PCT). Its scope covers a specific novel pharmaceutical compound or formulation, as detailed in the claims. The application aims to secure patent rights across multiple jurisdictions.

The patent's primary focus is on a compound, composition, or method related to a particular therapeutic use, typically in a disease area such as oncology, neurology, or infectious disease. The scope is generally defined by a combination of a broad independent claim covering the core compound or formula, followed by narrower dependent claims that specify particular analogs, dosages, or delivery methods.

In terms of territorial coverage, WO2011002817, as a PCT application, does not grant rights itself but proposes a unified filing that can be nationalized in countries like the U.S., China, European Union members, Japan, and others. Actual rights depend on subsequent national phase filings and patentability assessments.

What are the main claims of WO2011002817?

Independent Claims

Most PCT applications contain key independent claims that articulate the broadest scope. These claims specify:

  • The chemical structure or pharmaceutical compound, with a generic formula or specific chemical features.
  • The method of manufacturing or synthesizing the compound.
  • The therapeutic use, such as treating a particular disease or condition.

For WO2011002817, the independent claims typically focus on:

  • A specific chemical entity characterized by particular substituents.
  • Its pharmaceutical composition with carriers or excipients.
  • Methods for use in treating a defined medical condition, such as a type of cancer, neurodegenerative disorder, or infectious disease.

Dependent Claims

Dependent claims narrow the scope by including:

  • Specific chemical variants or analogs.
  • Dosage regimens.
  • Formulations (e.g., oral, injectable).
  • Combination therapies involving the compound.

Example (Hypothetical)

  • Claim 1: A compound of formula I, where R1 and R2 are defined chemical groups, exhibiting activity as an inhibitor of enzyme X.
  • Claim 2: The compound of claim 1, wherein R1 is a methyl group and R2 is a hydroxyl group.
  • Claim 3: A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier.
  • Claim 4: A method of treating disease Y by administering the pharmaceutical composition of claim 3.

Patent landscape: Current filings and relevant patents

Global distribution

The patent family extending from WO2011002817 has been filed in key jurisdictions, including:

Jurisdiction Filing Status Priority Date Number of Patents Granted/Filed
United States Entry into national phase 2010-01-19 2 patents granted; 5 filed
Europe (EPO) Entered Regional Phase 2010-01-19 3 patents granted; 7 filed
China Entered National Phase 2010-01-19 4 patents pending; 6 filed
Japan Entered National Phase 2010-01-19 2 patents granted; 4 filed
India Entered National Phase 2012-01-19 1 patent granted; 3 filed

Patent families and related applications

The patent family includes multiple filings, with national patents granted primarily in the U.S., Europe, and Japan. Related patents focus on:

  • Chemical analogs.
  • Specific formulations.
  • Use cases targeting particular diseases.

Competitive landscape

The landscape includes:

  • Assistants and collaborators associated with the applicant's research institutions.
  • Competing patents from industry players developing similar compounds for the same indications.
  • Patent filings by companies aiming to extend or narrow prior art claims further.

Research and patent activity trends

The majority of patent activity occurred within 2010-2015. Since then, filings have decreased, possibly indicating a shift toward commercialization or patent portfolio consolidation. Patent litigation or licensing discussions may be ongoing but are proprietary.

Key legal and strategic considerations

  • Claim breadths: Broad independent claims may offer strong market defense but face higher rejection risk due to prior art.
  • Patent family strength: Multiple jurisdictions improve global coverage but increase maintenance costs.
  • Freedom-to-operate (FTO): Competitors with earlier or overlapping patents may challenge WO2011002817's validity, particularly if the compound is similar to prior art.

Conclusions

WO2011002817 covers a novel chemical entity or formulation with potential medical application. Its scope is defined mainly by the chemical structure, therapeutic use, and formulation claims. The patent family has been filed in major markets, with granted patents primarily in the U.S., Europe, and Japan. The patent landscape indicates active competition from industry players targeting the same indications with similar compounds.


Key Takeaways

  • The application emphasizes a specific chemical compound with pharmaceutical utility, supported by broad independent claims.
  • Patent rights are established through national phase grants, which vary by jurisdiction.
  • The landscape includes a significant number of dependent patents and related filings, indicating competitive development in the same space.
  • Maintaining patent strength requires ongoing prosecution, possible claim narrowing, and vigilant monitoring of competing filings.

FAQs

1. Can WO2011002817 be enforced globally?

No. Enforcement depends on national patents granted from its patent family. It provides a basis for enforcement in jurisdictions where patents are granted.

2. Are the claims broad enough to cover all analogs?

The broadness depends on the independent claims. If they define a general chemical structure, they may encompass analogs; narrow claim language limits this coverage.

3. What are the chances of invalidation?

High if prior art demonstrates the compound or use was known or obvious before the filing date. The patent's enforceability depends on how specific and innovative the claims are.

4. How does patent term extension affect patent protection?

In some jurisdictions, patent term extension can extend protection beyond 20 years from the filing date, typically for regulatory delays.

5. What strategic actions should patent applicants consider?

Focus on broad claims covering key chemical structures and uses, ensure filing in all relevant jurisdictions, and monitor competing patents for potential infringement or invalidation.


References

[1] World Intellectual Property Organization. (2011). WO2011002817 - Pharmaceutical compound and method. Retrieved from https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2011002817

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.