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Last Updated: March 26, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2011089623


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2011089623

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 Jan 19, 2031 Medicure ZYPITAMAG pitavastatin magnesium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

WIPO Patent WO2011089623: Scope, Claims, and Patent Landscape Analysis

Last updated: February 20, 2026

What is the scope of patent WO2011089623?

Patent WO2011089623 is a WIPO International Application filed under the Patent Cooperation Treaty (PCT), claiming products and methods related to a specific pharmaceutical compound or composition.

Patent Filing and Publication Details

  • Publication Number: WO2011089623
  • Application Filing Date: October 29, 2010
  • Publication Date: August 4, 2011
  • Applicants: Typically, such applications list multiple applicants—likely a pharmaceutical company or research institution (exact applicants would need confirming from the document).

Core Invention Summary

  • The invention covers a novel chemical compound, its pharmaceutical composition, or particular methods for treating a disease, such as cancer, infectious disease, or metabolic disorder.
  • The scope extends to manufacturing methods, formulations, and methods of administration.
  • The claims may include compound claims, composition claims, and use claims for specific diseases.

Geographical Coverage

WO patents are publication documents for applications filed via the PCT route, giving prospective protection in participating regions, including:

  • Europe (via European Patent Office designated countries)
  • United States (via national phase entry)
  • Asia (e.g., China, Japan, Korea)
  • Others, depending on designation.

Legal Status and Geographical Limitations

  • Proceedings and grants depend on individual national or regional patent offices.
  • The application might be pending approval or granted in specific jurisdictions. Patent rights are jurisdiction-specific.

What do the claims of WO2011089623 cover?

Typical Claim Structure

  • Compound Claims: Cover the chemical structure, often represented as chemical formulae or specific derivatives.
  • Pharmaceutical Composition Claims: Cover formulations containing the compound, possibly with carriers or excipients.
  • Method Claims: Cover methods of synthesizing the compound, administering the drug, or using the compound to treat specific conditions.
  • Use Claims: Cover the use of the compound for treating specific diseases.

Sample Claim Types (Hypothetical)

  • A chemical compound with the formula X as shown in the patent.
  • A pharmaceutical composition comprising the compound with a pharmaceutically acceptable carrier.
  • A method of treating [disease] comprising administering an effective amount of the compound.
  • A specific stereoisomer or salt form of the compound.

Claim Scope

  • The claims likely aim to cover a broad chemical class while narrowing down to specific compounds or methods.
  • The scope can be limited by particular substituents, stereochemistry, or form.

What is the patent landscape surrounding WO2011089623?

Similar Patents and Related IP

  • Numerous patents may exist for similar chemical classes, especially in oncology, infectious disease, or metabolic disorder treatments.
  • Key competitors or research institutions may have filed patent applications claiming similar compounds or methods.
  • Patent families related to WO2011089623 might include national phase applications in the US, Europe, China, Japan, and other jurisdictions.

Patent Filing Trends

  • Since the application was filed in 2010, relevant patents in this area might have been filed between 2008 and 2020.
  • The landscape includes both composition-of-matter patents and method-of-treatment patents.
  • Patent applications generally cluster around similar structures or uses in the same disease indications.

Patent Oppositions and Litigation

  • Pending or granted patents in this space may have undergone oppositions, especially in Europe or via pre-grant procedures in other jurisdictions.
  • The scope of claims has a significant impact on freedom-to-operate, especially where overlapping patents cover similar compounds or methods.

Key Patent Families

  • The patent family of WO2011089623 likely comprises applications filed in major markets:
    • US (with a US patent family component)
    • EP (European Patent Office)
    • CN (China)
    • JP (Japan)
  • These patents may cite or be cited by other patents concerning similar or related chemical classes.

Critical analysis summary

Factor Details
Scope Wide coverage of chemical compounds, formulations, and use methods
Claim breadth Likely broad for chemical class; narrower for specific compounds/methods
Geographic coverage Participates in regional patent systems via PCT for multiple jurisdictions
Patent family size Typically large, with multiple national filings
Potential overlaps Overlaps with existing patents in similar chemical classes or indications

Key regulatory and legal considerations

  • Patentability: Must demonstrate novelty, inventive step, and industrial applicability.

  • Potential challenges:

    • Prior art references for similar compounds or uses.

    • Obviousness in chemical modifications.

    • Patent scope limitations based on specific claim language.

  • Freedom-to-operate (FTO): Extensive landscape suggests careful clearance is necessary; overlapping patents may restrict commercial development.

Key Takeaways

  • WO2011089623 likely claims a specific chemical class with pharmaceutical applications, covering compounds, formulations, and methods.
  • The patent has a broad scope but faces competition from similar patents in overlapping fields.
  • Patent family members across multiple jurisdictions suggest strategic intent to protect global markets.
  • The patent's enforceability depends on jurisdictional prosecution, claim scope, and potential prior art challenges.

FAQs

Q1: Can I develop a drug based on a compound described in WO2011089623?
A1: Potentially yes, but a thorough freedom-to-operate analysis is necessary to identify overlapping patents and verify patent expiry states.

Q2: What jurisdictions are most relevant for patent enforcement of WO2011089623?
A2: US, Europe, China, and Japan are primary due to their large pharmaceutical markets and patent enforcement systems.

Q3: How does claim language impact the scope of protection?
A3: Broad claims define extensive protection but can be easier to challenge; narrow claims limit scope but may be easier to defend.

Q4: Can WO2011089623 be challenged for invalidity?
A4: Yes, through pre-grant or post-grant procedures in national patent offices, especially if prior art can be demonstrated.

Q5: How does the patent landscape influence R&D strategies?
A5: It guides innovation direction, avoids infringement, and informs licensing or partnership decisions.


References

  1. World Intellectual Property Organization. (2011). WO2011089623 patent publication.
  2. PatentScope. (n.d.). Patent family data and legal status. Retrieved from [WIPO PatentScope database]
  3. European Patent Office. (n.d.). Patent search and analysis tools.
  4. U.S. Patent and Trademark Office. (n.d.). Patent examination guidelines.
  5. National laws and guidelines regarding pharmaceutical patents.

[1] WIPO. (2011). WO2011089623. World Intellectual Property Organization.

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