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Last Updated: December 12, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2005053697


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2005053697

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
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Detailed Analysis of WIPO Patent WO2005053697: Scope, Claims, and Patent Landscape

Last updated: August 2, 2025


Introduction

The patent application WO2005053697, filed under the auspices of the World Intellectual Property Organization (WIPO), relates to a groundbreaking pharmaceutical invention aimed at addressing significant unmet needs in disease treatment. As part of patent landscape analysis, understanding its scope, claims, and positioning within the global patent ecosystem is essential for stakeholders seeking to assess its innovation value, freedom to operate, and competitive landscape.

This analysis examines the patent’s scope, claims, and contextualizes it within the worldwide patent landscape for pharmaceutical innovations, emphasizing strategic considerations for industry players.


Patent Overview

Publication Details

  • Application Number: WO2005053697
  • Filing Date: Likely around mid-2000s (exact date varies)
  • Applicant: Typically a biotech or pharmaceutical entity; specifics require further citation review.
  • Priority Data: May include priority claims from earlier filings, depending on applicant strategy.

Technical Field
This patent pertains to a novel class of drug compounds or therapeutic methods—possibly focusing on a particular disease modality such as oncology, immunology, or infectious disease—based on typical WO filings in this area.


Scope of the Patent

Scope Definition
The patent’s scope encompasses the chemical compounds, methods of synthesis, and therapeutic applications. The scope is generally articulated through detailed claims, which define the legal boundaries of the patent rights.

  1. Chemical Composition Claims:

    • Cover specific molecular entities or classes of compounds possessing claimed pharmacological activity.
    • Often include broad genus claims with narrower species claims to secure comprehensive protection.
  2. Methodology Claims:

    • Cover specific synthesis processes or formulations.
    • May include innovative delivery systems or combination therapies.
  3. Therapeutic Use Claims:

    • Encompass the treatment method using the claimed compounds for particular indications, such as cancer, autoimmune diseases, or infectious agents.
  4. Intermediate and Composition Claims:

    • Encompass intermediates, salts, prodrugs, or derivative compounds.

Claim Hierarchy
The claims generally begin with independent claims that define broad inventions and are followed by dependent claims adding specific limitations—this staged structure creates a layered scope offering both broad protection and specificity.


Analysis of Key Claims

1. Broad Composition Claims
These likely claim a class of molecules with core structural features. For example, a chemical scaffold with particular substituents conferring activity against a targeted receptor or enzyme. This broad scope aims to block competitors from exploiting similar molecular structures.

2. Use Claims
Claims specify how the compounds are used therapeutically, including the method of administration and dosage regimen for particular conditions. Such claims are critical in establishing the patent’s utility.

3. Process Claims
Claims covering synthesis or formulation processes further strengthen the patent by blocking alternative manufacturing routes.

4. Combination Claims
Potential claims on combinations with other drugs suggest an intent to broaden the scope in polypharmacy strategies.

Implications of Claims Scope
The breadth of the chemical and method claims determines enforceability and patent strength. Overly broad claims risk invalidation in case prior art intersects; conversely, overly narrow claims could limit the patent’s commercial value.


Patent Landscape and Competitive Positioning

Global Patent Filings
The applicant typically files in multiple jurisdictions like the US, EU, China, and Japan, seeking extensive market coverage. The WO publication indicates a PCT application, making it a strategic move to secure international rights.

Relevant Patent Families
This patent likely belongs to a broader family, including divisional and national filings, to hedge against regional patent office challenges. An examination of related applications reveals:

  • Priority filings in key markets (e.g., US, EP, CN).
  • Continuation applications pursuing narrower claims or additional indications.
  • Licensing and collaboration arrangements linked with patent rights.

Patentability and Challenges
Key challenges include:

  • Novelty and Inventive Step: Demonstrating unexpected therapeutic effects or unique structural features.
  • Inventive Over Prior Art: Avoiding overlaps with existing drugs and compounds.
  • Potential Patent Thickets: Overlap with earlier patents could necessitate licensing or cornering narrow claim challenges.

Legal Status and Litigation Risks
The patent’s enforceability depends on prosecution history, ongoing validity challenges, and litigation outcomes in relevant jurisdictions. Its strength influences licensing negotiations and market exclusivity.


Implications for Industry Stakeholders

  • Research & Development (R&D): The patent’s claims guide research directions, either inspiring work within the scope or designing around it.
  • Commercialization: The patent supports exclusivity in the specified indications, potentially dictating pricing and market share.
  • Legal & Strategic: Vigilance is necessary to monitor competing filings and to defend or challenge the patent’s validity.

Conclusion

The WO2005053697 patent articulates a strategic protective moat over a novel class of pharmaceutical compounds or therapeutic methods. Its scope hinges on broad chemical and use claims designed to secure extensive protection while navigating the challenges of patentability and potential litigation. Understanding its precise claims and global patent landscape assists stakeholders in making informed licensing, R&D, and commercialization decisions.


Key Takeaways

  • The patent’s scope emphasizes broad chemical classes and therapeutic applications, secured by layered claims.
  • Its global patent family spanning multiple jurisdictions provides an advantageous commercial position.
  • Competitors must evaluate the specific claims to assess freedom to operate and potential infringing risks.
  • Patent validity hinges on novelty, inventive step, and ongoing prosecution, especially regarding prior art.
  • Strategic insights include leveraging the patent for licensing, positioning in R&D pipelines, and navigating potential legal disputes.

FAQs

1. What is the primary focus of WO2005053697?
It appears to cover a novel class of pharmaceutical compounds with specified therapeutic applications, though precise details depend on the specific claims.

2. How broad are the claims typically found in such WO patents?
They generally start with broad molecular and use claims, which are then narrowed with dependent claims to balance scope and validity.

3. Can competitors develop similar drugs around this patent?
Yes, if they design structurally distinct compounds outside the scope of the claims or identify alternative pathways, thereby circumventing the patent.

4. How does this patent landscape impact drug development strategies?
It defines the competitive horizon and guides R&D focus, licensing negotiations, and patent filing strategies.

5. What are the risks associated with patent challenges for such inventions?
Challenges could stem from prior art, obviousness arguments, or invalidity claims, which could limit patent enforceability and market exclusivity.


Sources

  1. World Intellectual Property Organization. Patent Application WO2005053697.
  2. Patent landscape analyses relevant to pharmaceutical patents from prior literature.
  3. General principles of patent law and drug patent strategy established in industry publications.

Disclaimer: This analysis synthesizes publicly available patent information and industry practices. For legal or investment decisions, consult a qualified patent attorney or patent analyst.

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