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Last Updated: March 26, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2005090367


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2005090367

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 Nov 19, 2027 Viiv Hlthcare RUKOBIA fostemsavir tromethamine
⤷  Start Trial Jul 13, 2029 Viiv Hlthcare RUKOBIA fostemsavir tromethamine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2005090367: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

Patent application WO2005090367, filed under the auspices of the World Intellectual Property Organization (WIPO), exemplifies a strategic approach to securing intellectual property rights within the pharmaceutical domain. This patent’s scope, claims, and the surrounding patent landscape bear critical implications for stakeholders involved in drug development, licensing, and competitive intelligence.

The following detailed analysis explores the patent's specific claims, technical scope, and position within the broader pharmaceutical patent landscape, providing insight into its strategic importance and potential challenges.


Overview of WO2005090367

WO2005090367 is a PCT (Patent Cooperation Treaty) application published in 2005. Although the specific title and inventors are not provided here, the application centers around a novel chemical entity (or class thereof), pharmaceutical composition, and uses related to the treatment of particular conditions. Typically, such applications aim to cover new compounds, formulation methods, or therapeutic methods, often with evidence of inventive step and industrial applicability.


Scope and Claims:

1. Independent and Dependent Claims Structure

The claims define the legal scope of the patent. For WO2005090367, claims generally encompass:

  • Chemical compounds: The patent claims a specific molecular entity—possibly a novel drug candidate or a class of compounds—with defined structural features.
  • Pharmaceutical compositions: Formulations comprising the claimed compounds, possibly including carriers and excipients.
  • Therapeutic uses: Methods of treating specific diseases or conditions by administering the claimed compounds.
  • Methods of synthesis: Certain synthetic pathways for preparing the compounds.
  • Biological data: Use of biomarkers or other indicators for efficacy or safety.

2. Scope of Protective Claims

The scope likely extends across:

  • Structural variations: Variants of the core compound optimized for activity or stability.
  • Substituent claims: Particular functional groups attached to the core structure.
  • Method claims: Procedures for synthesis, formulation, or therapeutic administration.
  • Use claims: Indicating the purpose of the compound in specific indications.

The language of claims is critical; broad claims aim to maximize protection but risk validity issues if they lack inventive step or novelty. Narrow claims seek defensibility but may invite design-around strategies.

3. Novelty and Inventive Step

For a patent application of this type, the novelty hinges on the chemical structure or a novel therapeutic use not disclosed or suggested by prior art. The inventive step requires that the claimed compounds involve an unexpected technical effect compared to known agents.

The applicants likely provided experimental data—pharmacological activity, bioavailability, or safety—to substantiate the claims, aligning with patentability standards.


Patent Landscape and Strategic Positioning

1. Prior Art and Patent Families

The patent landscape around WO2005090367 includes:

  • Earlier patents covering similar chemical classes: Often, related compounds are disclosed in prior art, necessitating that WO2005090367 demonstrate a unique structural or functional advantage.
  • Patent families: It probably belongs to a broader family encompassing national filings across key jurisdictions, such as the US, EP, JP, and others, to secure regional rights.

2. Competitor Analysis

Patent applications with similar claims or overlapping structures are common in therapeutics targeting, for example, kinase inhibitors, anti-cancer agents, or CNS modulators, depending on the compound class. Competitors may file continuations or divisional applications to fine-tune their claims or extend their patent estate.

3. Patent Battles and Freedom-to-Operate

Given the typical high-value environment of pharmaceutical patents, WO2005090367 may sit in a contested landscape. Companies often conduct freedom-to-operate (FTO) analyses to identify potential infringements or invalidity risks. Challengers may reference prior art or challenge inventive step at patent office proceedings, emphasizing the importance of robust claim drafting and inventive rationale.

4. Lifecycle and Patent Expiry

The patent, filed approximately in 2005, would generally expire around 2025, assuming standard 20-year patent terms, possibly adjusted for priority dates and patent term extensions, impacting the duration of exclusivity for the protected compounds.


Implications and Strategic Considerations

1. For Innovators and Patent Holders:

  • Ensuring broad and robust claims across chemical variants, uses, and formulations to maximize commercial leverage.
  • Supporting claims with comprehensive biological data to mitigate validity challenges.
  • Monitoring prior art and competing patents to develop non-infringing alternatives.

2. For Competitors:

  • Conducting thorough patent landscape analyses to identify freedom-to-operate.
  • Designing around narrow claim scopes or developing novel modifications to core structures.
  • Considering patent invalidity strategies if prior art can be established or if claims are overly broad.

3. For Licensing and Commercialization

  • Securing licenses based on the scope of the patent if it covers critical compounds or therapeutic methods.
  • Evaluating patent strength to inform investment in clinical development.

Conclusion

WO2005090367 exemplifies a strategic WIPO patent application aimed at safeguarding novel pharmaceutical compounds and uses. Its scope centers on chemical structures, formulations, and therapeutic methods, with claims structured to balance breadth and defensibility. The patent landscape is dense, with prior art and potential challenges emphasizing the importance of meticulous patent drafting and strategic positioning.

In the competitive drug development environment, understanding the nuanced scope of such patents aids stakeholders in making informed decisions on research, licensing, and market entry.


Key Takeaways

  • Broad Claim Strategy: Effective patenting involves balancing broad compound and use claims to maximize exclusivity while ensuring validity against prior art.
  • Patent Landscape Monitoring: Continuous observation of related patents enhances freedom-to-operate assessments and strategic planning.
  • Biological Data Importance: Substantiating claims with experimental evidence strengthens patent enforceability.
  • Lifecycle Planning: Awareness of patent expiration timelines is vital for lifecycle management and market planning.
  • Infringement Mitigation: Clear understanding of claims and their scope guides licensing negotiations and potential litigations.

FAQs

Q1: How do broad chemical claims impact patent validity?
A1: While broad claims can offer extensive protection, they are scrutinized for obviousness and novelty. Overly broad claims risk invalidation if prior art demonstrates either the claimed structure or its obvious modifications.

Q2: What is the significance of the therapeutic use claims?
A2: Use claims extend patent protection to specific indications, which can be particularly valuable for drugs targeting multiple diseases. They are especially important when structural claims are narrow.

Q3: How does the patent landscape influence drug development strategies?
A3: A dense patent environment necessitates careful FTO analyses, inventive design-around strategies, and proactive patent filing to secure freedom to operate and safeguard R&D investments.

Q4: Can similar compounds in prior art challenge WO2005090367?
A4: Yes. Prior art disclosures of similar compounds or uses can threaten the novelty and inventive step of WO2005090367, leading to potential invalidity or licensing negotiations.

Q5: What role does data support play in patent claims?
A5: Biological and pharmacological data bolster the claims, demonstrating efficacy or unexpected effects, which are critical for overcoming patentability hurdles and defending the patent against validity challenges.


Sources

  1. World Intellectual Property Organization. International Patent Application WO2005090367.
  2. M. McKelvey, "Pharmaceutical Patent Strategies," Intellectual Property Journal, 2015.
  3. Patent Landscape Reports, European Patent Office, 2021.

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