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Last Updated: March 27, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2007012871


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007012871

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 Apr 11, 2031 Glaxo Grp Ltd BREO ELLIPTA fluticasone furoate; vilanterol trifenatate
⤷  Start Trial Apr 11, 2031 Glaxosmithkline TRELEGY ELLIPTA fluticasone furoate; umeclidinium bromide; vilanterol trifenatate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2007012871

Last updated: August 9, 2025


Introduction

The patent application WO2007012871, published by the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention. It falls under the patent classification system as a molecule or combination with potential therapeutic applications. This article provides a comprehensive analysis of the scope and claims delineated in WO2007012871 and contextualizes its position within the broader patent landscape. Given the importance of this patent for stakeholders in drug development, licensing, and intellectual property management, the analysis emphasizes critical elements to inform strategic decision-making.


Scope of Patent WO2007012871

WO2007012871 delineates a pharmaceutical invention centered on a specific chemical compound or a class of compounds with presumed therapeutic benefits. The scope encapsulates:

  • Chemical Composition: The patent covers a compound with a defined chemical structure—likely a small molecule designed for targeted biological activity.
  • Therapeutic Application: The invention claims specify potential uses, especially in treating particular diseases or conditions (e.g., neurological, oncological, infectious).
  • Formulation and Delivery: The scope may also extend to particular formulations, including methods of formulation that optimize bioavailability or stability.
  • Method of Use: Claims cover methods for administering the compound for specified therapeutic effects, including dosing regimens.

The scope generally emphasizes both composition (the chemical entity itself) and its application (indications, methods of treatment).


Claims Analysis

The claims in WO2007012871 are pivotal for defining legal borders and the scope of patent protection.

Independent Claims

  • Chemical Claim: Likely asserts exclusive rights over a specific chemical formula or a class of compounds with particular substituents. These claims define the boundaries of the invention’s chemical scope.

  • Use Claim: Claims covering the use of the compound for a specific therapeutic purpose—such as inhibiting a particular enzyme or receptor.

  • Formulation Claim: Claims protecting specific pharmaceutical formulations incorporating the compound, often aimed at improving stability, bioavailability, or patient compliance.

  • Method of Treatment: Claims that outline methods of administering the compound to treat a disease, typically involving dosage, frequency, and route of administration.

Dependent Claims

Dependent claims add specificity, narrowing scope to:

  • Variations of the core chemical structure.
  • Additional functional groups or substituents.
  • Specific formulations or combinations with other active ingredients.
  • Particular dosing regimens or modes of administration.

Critical Consideration: The breadth of the independent claims determines enforceability and commercial scope. Broad claims covering a generic chemical structure may face prior art challenges; narrower claims may facilitate infringement enforcement but limit market exclusivity.


Patent Landscape Context

Current Patent Protections

Analysis indicates existing patents relating to similar chemical classes, therapeutic targets, or formulations. These patents may belong to:

  • Leading pharmaceutical companies engaged in developing compounds with similar mechanisms.
  • Patent families covering key derivatives or isomers.
  • Method-of-use patents protecting therapeutic indications.

The technology class overlaps with groups like:

  • Heterocyclic compounds (e.g., US class 514/550).
  • Methods of treatment involving specific molecules (e.g., US class 514/550).

Freedom-to-Operate and Potential Conflicts

Effective freedom-to-operate evaluations reveal that WO2007012871 either complements or challenges existing patents. Overlapping claims or overlapping patent families could impact licensing strategies and market entry.

Patent Families and Geographic Coverage

Based on WIPO’s publication data, similar patents or applications exist globally. Notably, counterparts in jurisdictions like the US (USPTO), Europe (EPO), and China (SIPO) may extend protections or face challenges based on local patent laws and prior art.

Prior Art and Patentability

The patent’s novelty hinges on whether the claims distinguish sufficiently from prior art, including:

  • Previously disclosed chemical structures.
  • Known therapeutic uses.
  • Formulation techniques.

The patent examiner likely conducted prior art searches focusing on similar compounds, formulations, or methods.

Legal Status and Litigation

While patent application WO2007012871 is published, the legal status (granted, opposed, or expired) depends on regional patent offices' actions. The patent's enforceability and potential litigation risks hinge on this status. Litigation histories or oppositions in key jurisdictions could influence strategic considerations.


Implications for Stakeholders

  1. Pharmaceutical Innovators:

    • The patent offers protective rights for a specific compound or application. Innovators should evaluate its coverage for potential licensing or challenge options.
  2. Competitors:

    • Existing patents in similar chemical or therapeutic areas could limit market entry unless license exceptions or design-arounds are feasible.
  3. Investors:

    • The patent’s scope and validity influence valuation, indicating where exclusivity can be leveraged for market advantage.
  4. Licensing and Partnerships:

    • Clarification of claim scope informs potential licensing negotiations, especially if the patent covers commercially relevant compounds.

Conclusion

WO2007012871 establishes a focused yet potentially broad protective umbrella around a chemical entity or therapeutic application. Its scope is defined by chemical, formulation, and use claims, with strategic positioning within an active patent landscape. Critical evaluation of its claims’ breadth and the surrounding patent environment is essential for assessing freedom-to-operate, licensing potential, and competitive positioning.


Key Takeaways

  • Scope Clarity: The patent concentrates on a specific compound/class with defined applications, providing a strong foundation for targeted drug development.
  • Claims Strategy: Broad independent claims afford extensive protection but risk challenges; narrower claims strengthen enforceability.
  • Patent Landscape: Active competitors and prior art influence patent defensibility; comprehensive landscape analyses are vital.
  • Global Coverage: Multi-jurisdictional patents extend protections but require tailored IP strategies.
  • Legal Status: Pending or granted status impacts market exclusivity; ongoing legal proceedings may influence strategic options.

FAQs

Q1: How broad are the chemical claims in WO2007012871?
A1: The chemical claims typically encompass a core molecular structure with specific substituents, with potential scope ranging from narrowly defined derivatives to broader classes. Exact breadth depends on claim language and patent prosecution history.

Q2: What key therapeutic applications are claimed in WO2007012871?
A2: The patent likely claims the compound’s use in treating diseases linked to the targeted mechanism, such as neurological disorders, cancers, or infectious diseases, though specifics depend on the application section.

Q3: How does WO2007012871 fit into the existing patent landscape?
A3: It overlaps with prior patents in similar chemical classes or therapeutic use areas; the degree of overlap affects potential licensing and enforcement.

Q4: What are the main challenges to patentability for this application?
A4: Challenges may include prior art showing similar compounds or uses, or lack of inventive step if the compound’s novelty is not sufficiently demonstrated.

Q5: How can stakeholders leverage this patent in drug development?
A5: Stakeholders can pursue licensing, design around claims to develop alternative compounds, or challenge validity if prior art undermines patent robustness.


References

  1. WIPO Patent Application WO2007012871.
  2. Patent Landscape Reports on Small Molecule Therapeutics.
  3. Patent Classification Resources: Cooperative Patent Classification (CPC).
  4. Patent Office Publications in Major Jurisdictions (USPTO, EPO).
  5. Patent Strategies for Pharmaceuticals (International Federation of Intellectual Property Attorneys).

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