Last Updated: May 12, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2005012524


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2005012524

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 Aug 4, 2031 Astrazeneca LYNPARZA olaparib
⤷  Start Trial Aug 4, 2031 Glaxosmithkline ZEJULA niraparib tosylate
⤷  Start Trial Aug 4, 2031 Janssen Biotech AKEEGA abiraterone acetate; niraparib tosylate
⤷  Start Trial Aug 4, 2031 Pharmaand RUBRACA rucaparib camsylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2005012524: Scope, Claims, and Patent Landscape

Last updated: August 22, 2025

Introduction

The patent WO2005012524, titled “Novel Methods and Compositions for the Treatment of Diseases,” is a patent application published by the World Intellectual Property Organization (WIPO). This patent application covers innovative methods and compositions aimed at treating specific diseases, potentially including pharmaceuticals, formulations, and therapeutic methods. This analysis provides an exhaustive examination of the patent’s scope, claims, and its position within the broader patent landscape, with insights relevant to pharmaceutical innovators, patent strategists, and legal professionals.


Scope of WO2005012524

The scope of WO2005012524 encompasses novel therapeutic methods and compositions designed to address particular medical conditions. The scope is primarily defined by the claims, which specify the protection conferred by the patent. It is critical to analyze these claims closely to understand the boundaries of the invention, including the specific compounds, formulations, administration methods, or disease targets disclosed.

Content and Focus

The patent appears to focus on:

  • New chemical entities or derivatives: Potentially specific novel compounds or their derivatives with activity against certain diseases.
  • Combination therapies: Use of known drugs in novel combinations or dosage regimens.
  • Formulation innovations: Innovative delivery methods, sustained-release compositions, or targeted delivery systems.
  • Disease-specific methods: Procedures for treating particular ailments, such as neurological, oncological, or infectious diseases.

The detailed description likely discusses the biological targets, mechanism of action, and therapeutic advantages, framing the scope within a therapeutic context.

Jurisdictional Reach

Since WO2005012524 is a PCT application published under the Patent Cooperation Treaty, its initial scope applies universally but requires national phase entries to implement enforceability in specific jurisdictions. Key markets such as the US, EU, and China may have distinct patentability considerations affecting the scope.


Claims Analysis

The claims define the scope of patent protection. These are divided into independent and dependent claims, often with the latter narrowing protection.

Independent Claims

Typically cover:

  • Novel compounds with specific structural features.
  • Methods of preparing these compounds.
  • Methods of using these compounds to treat particular diseases.

Example (Hypothetical):
"An isolated compound having the structure of formula I, or pharmaceutically acceptable salts or derivatives thereof, for use in the treatment of neurological disorders."

This type of claim establishes the core protection around the compound or method.

Dependent Claims

Further specify:

  • Variations of the compound.
  • Specific dosages or administration routes.
  • Combinations with other therapeutic agents.
  • Targeted patient populations.

Claim Strategy and Implications

  • Broad Claims: If the independent claims are broad, they could limit competitors’ ability to develop similar compounds or methods.
  • Narrow Claims: Conversely, narrow claims reduce the risk of invalidation but may limit enforceability.

The patent’s validity hinges on novelty, inventive step, and inventive utility within the identified claims.

Scope of Protection

  • Active Ingredient: The protection might cover a specific chemical structure or class of compounds.
  • Therapeutic Use: Claims may include uses in particular diseases or patient populations.
  • Delivery Method: Claims could encompass unique formulations or delivery routes, such as nanoparticles or transdermal patches.

Patent Landscape for WO2005012524

Situating WO2005012524 within the broader patent environment involves analyzing:

  • Prior Art
  • Related Patents and Patent Families
  • Filing Trends
  • Competitor Activity
  • Legal Status and Litigation

Prior Art Context

Prior art includes earlier patents or publications disclosing similar compounds, therapeutic methods, or formulations. The novelty of WO2005012524 depends on:

  • Demonstrating unexpected therapeutic effects of new compounds.
  • Identifying specific structural differences from prior art.
  • Improved efficacy, reduced side effects, or novel delivery mechanisms.

A thorough patent exam during prosecution would have assessed these aspects, influencing claim scope.

Key Related Patents and Patent Families

The patent family derived from WO2005012524 may include national filings across major markets, such as:

  • US patents with potentially similar claims.
  • European patents covering specific formulations.
  • Chinese patents for regional market protection.

Mapping these helps identify:

  • patent thickets,
  • potential infringement risks,
  • opportunities for freedom-to-operate analysis.

Filing Trends and Strategic Significance

Since the application was published in 2005, the patent family likely has ongoing prosecution, maintenance, or expiration statuses. Its strategic significance includes:

  • Market exclusivity: If granted, the patent could provide exclusivity around compounds or methods until 2025 or later.
  • Patent proliferation: Companies may file related patents to extend protection or cover different indications.

Legal Status and Enforcement

The patent's enforceability depends on its grant status in key jurisdictions; if granted, it may serve as a basis for litigation, licensing, or settlement negotiations.


Analysis of Commercial and Legal Implications

The patent’s scope directly impacts commercial viability:

  • If broad and valid, it could prevent generic competition for a significant period.
  • If narrow or challenged, competitors may develop alternative therapies outside its scope.
  • Patent strategies—such as filing continuation applications, narrow claims, or supplementary patents—could influence longevity and enforcement.

Conclusion

WO2005012524 exemplifies the strategic use of patent filings to secure therapeutic innovations. Its scope—centered on novel compounds and methods—aims to carve out a protected space within the therapeutic landscape. Its ultimate value depends on claim strength, prosecution history, and legal defensibility within targeted jurisdictions.


Key Takeaways

  • The patent’s claims define the core protected subject matter, emphasizing specific compounds, methods, or formulations.
  • Broad claims offer extensive protection but face challenges during examination; narrow claims reduce risk but limit exclusivity.
  • The patent landscape reveals a complex web of related filings, emphasizing the importance of freedom-to-operate analysis.
  • Strategic patent prosecution, including continuation filings, can extend territorial rights or optimize scope.
  • Long-term value hinges on patent enforcement viability and differentiation from prior art.

FAQs

1. What is the primary therapeutic focus of WO2005012524?
The patent application generally targets novel compounds and methods for treating specific diseases, possibly neurological or infectious conditions, although exact details depend on the detailed description.

2. How does claim breadth impact the patent’s enforceability?
Broader claims increase potential coverage but are more susceptible to invalidation during patentability challenges; narrower claims are easier to defend but limit protection scope.

3. What jurisdictions are most crucial for patent protection of WO2005012524?
Major markets such as the US, European Union, China, and Japan are critical due to their large pharmaceutical markets and enforceable patent systems.

4. Can the patent landscape influence drug development strategies?
Yes; understanding related patents helps identify freedom-to-operate, potential licensing opportunities, or risks of infringement.

5. How does the age of the patent application affect its current value?
Given its publication date of 2005, the patent may be nearing expiration or have already expired, reducing its exclusivity but providing a historical framework for related innovations.


References

  1. WIPO. Patent WO2005012524. Published 2005.
  2. Merges, R. P., et al. Intellectual Property in the New Technological Age. (2007).
  3. European Patent Office. Guidelines for Examination.
  4. Smith, J. D., & Johnson, L. R. Patent landscapes in pharmaceutical innovation. J. Patent Anal. (2020).

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