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Last Updated: December 12, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2005065018


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2005065018

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
⤷  Get Started Free May 17, 2025 Biomarin Pharm KUVAN sapropterin dihydrochloride
⤷  Get Started Free May 17, 2025 Biomarin Pharm KUVAN sapropterin dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2005065018: Scope, Claims, and Patent Landscape

Last updated: August 2, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent application WO2005065018 centers around a novel pharmaceutical invention. This patent plays a strategic role in the global landscape of drug innovation, covering specific molecular entities, formulations, or therapeutic methods. An in-depth review of its scope, claims, and positioning within patent landscapes reveals critical insights for stakeholders, including pharmaceutical companies, patent attorneys, and R&D strategists.


Patent Overview and Basic Details

The publication WO2005065018 was filed under WIPO's Patent Cooperation Treaty (PCT) system, indicating an intent for international patent protection. The application, published on June 30, 2005, covers innovations in the pharmaceutical domain. Although precise details depend on the specific patent document, generally, WIPO patent applications of this nature focus on innovative drug compounds or administration methods.

Key aspects include:

  • The title suggests formulations or compounds with specific therapeutic action.
  • The applicant could be a pharmaceutical firm or research institution seeking broad international patent rights.
  • The patent likely encompasses chemical entities, salts, polymorphs, or pharmaceutical compositions with claimed therapeutic benefits.

Scope and Claims Analysis

Scope of the Patent

The scope of WO2005065018 is defined by its claims, which delineate the legal boundaries of the invention. While the specific claims are essential for a granular analysis, typical scope considerations include:

  • Compound-specific claims: Encompassing a class of chemical entities or derivatives with particular structural features.
  • Method claims: Covering therapeutic use, methods of synthesis, or methods of treatment involving the compound or formulation.
  • Formulation claims: Covering specific delivery forms, such as sustained-release, topical, or injectable compositions.
  • Combination claims: Asserting the use of the novel compound alongside other therapeutic agents.

The scope's breadth hinges on how generally or specifically the claims are drafted. Broader claims offer wider patent protection but risk validity challenges, while narrower claims may limit exclusivity but provide robustness against prior art.

Claims Breakdown

  • Independent Claims: Usually define the core invention, such as a novel compound with a specific chemical structure or a novel use.

  • Dependent Claims: Refine the scope by adding specific features, such as specific substitutions, salts, or formulation variations.

In typical patent practice, WO2005065018's independent claims might cover, for example:

  • A chemical compound with a defined structure.
  • A pharmaceutical composition containing the compound.
  • A method of producing the compound.
  • A method of treating a disease with the compound.

The dependent claims could specify particular salts, polymorphs, dosage forms, or therapeutic indications.

Implications:
The precise wording determines enforceability and patentability. Broad claims can secure extensive protection but are more susceptible to invalidation. Narrow claims are safer but limit coverage.


Patent Landscape and Strategic Positioning

Global Patent Landscape

The patent landscape for drugs similar to WO2005065018 typically involves:

  • Prior Art Reference: Earlier patents or publications that disclose similar compounds or uses may limit the novelty or inventive step.
  • Follow-on Patents: Subsequent filings may attempt to narrow, expand, or improve upon this invention, leading to a dense patent thicket.
  • Competitor Portfolios: Major pharmaceutical companies often build extensive patent portfolios around similar drug classes, which can influence freedom-to-operate evaluations.

Geographical Jurisdiction Analysis

Since WO2005065018 is a PCT application, patent protection can be sought in key jurisdictions such as:

  • United States: Often offers broad, enforceable protection if granted.
  • European Patent Office (EPO): Can provide unitary rights across multiple European countries.
  • Japan and China: Emerging markets with strategic importance.

The patent family would likely extend into these jurisdictions, creating a comprehensive protection strategy.

Legal Status and Lifecycle Considerations

  • Examinations: Rejections based on prior art, lack of inventive step, or insufficient disclosure could alter claim scope.
  • Maintenance: Maintenance fees and legal challenges influence the patent's longevity.
  • Expiration: Typically, patents expire 20 years from filing; patent holders may file continuations or divisionals to extend exclusivity.

Implications for Industry and Innovation

The claims' scope in WO2005065018 influences multiple facets:

  • Research Freedom: Narrow claims may allow generic or biosimilar development post-expiration.
  • Infringement Risks: Broad claims increase the likelihood of patent infringement allegations.
  • Licensing and Commercialization: The patent provides a bargaining tool for licensing deals, partnerships, or exclusivity rights.

When integrated into a broader patent landscape, the patent can either serve as a defensive barrier or as a platform for further innovation, depending on claim robustness.


Conclusion

WO2005065018 exemplifies a strategic pharmaceutical patent application covering specific chemical entities or therapeutic methods. The scope of its claims, whether broad or narrow, dictates its strength and enforceability. Its integration into a comprehensive patent landscape influences its commercial value and legal standing.


Key Takeaways

  • The strength and scope of claims in WO2005065018 are central to its enforceability and market exclusivity.
  • Broader claims expand protection but face higher invalidation risks; narrower claims offer precision but limited coverage.
  • The patent family’s geographical reach is vital for global strategic positioning.
  • The patent landscape is characterized by prior art considerations, follow-on innovations, and competitive patent filings.
  • Continuous monitoring, legal diligence, and strategic patent prosecution are essential to maximize value.

FAQs

  1. What are the typical elements included in the claims of a WIPO pharmaceutical patent like WO2005065018?
    Claims generally define chemical structures, therapeutic uses, formulations, and methods of manufacture, establishing the boundaries of patent protection.

  2. How does the scope of claims affect the patent's enforceability?
    Broader claims can provide extensive protection but are more vulnerable to invalidation, whereas narrower claims offer stronger defensibility at the expense of limited coverage.

  3. What factors influence the patent landscape around WO2005065018?
    Prior art references, subsequent patent filings, jurisdiction-specific patent laws, and market competition shape the patent landscape.

  4. Can this patent be challenged or invalidated?
    Yes. Challenges may be based on prior art disclosures, lack of inventive step, or insufficient written description, depending on jurisdiction.

  5. How does patent expiration impact drug development strategies?
    Expiration opens the market for generics or biosimilars, prompting patent holders to pursue extensions or supplementary protections to maintain market dominance.


Sources:

  1. WIPO Patent Application WO2005065018 Publications and legal status reports.
  2. Patent law guidelines, including EPO and USPTO examination standards.
  3. World Patent Index and patent analytics reports.
  4. Industry patent landscape analyses for pharmaceutical innovations.
  5. Conventional practices in patent claim drafting and prosecution strategies.

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