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Last Updated: December 18, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 03061744


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 03061744

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
8,511,304 Dec 14, 2027 Glaxosmithkline ANORO ELLIPTA umeclidinium bromide; vilanterol trifenatate
8,511,304 Dec 14, 2027 Glaxo Grp Ltd BREO ELLIPTA fluticasone furoate; vilanterol trifenatate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO03061744: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

Patent WO03061744, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to an innovative pharmaceutical formulation or compound. This patent plays a strategic role in the evolving landscape of drug innovations, representing a significant patent claim in the targeted therapeutic area. This analysis offers in-depth insights into the scope, claims, and the broader patent landscape surrounding WO03061744 to inform stakeholders—including pharmaceutical companies, patent attorneys, and R&D strategists—about its scope, strength, and competitive positioning.


Scope of Patent WO03061744

Legal Coverage and Geographical Scope

Patent WO03061744 is a WIPO International Patent Application filed under the Patent Cooperation Treaty (PCT), which aims to secure patent rights across multiple jurisdictions through a single filing process. While WIPO applications do not in themselves grant patent rights, they serve as a basis for national phase entries in member countries, offering potential patent protection in over 150 jurisdictions.

The scope of the patent, once granted in individual jurisdictions, covers the specific drug compound, its formulations, or methods of use detailed in the application. The actual coverage encompasses the inventive features set forth in the claims, which determine the enforceable boundaries of the patent.

Technological Field

Based on available information, WO03061744 appears to relate to pharmaceutical compositions—possibly a novel drug molecule, a drug-target interaction, or a specific formulation strategy aimed at optimizing bioavailability, stability, or targeted delivery. The patent’s scope likely emphasizes the structural features of the compound, its method of synthesis, and its therapeutic application.

Innovative Aspects

The scope hinges on the novelty and inventive step of the claimed invention. These could involve:

  • Novel chemical structures or derivatives
  • Unique formulation techniques
  • Specific methods of delivering or administering the drug
  • Therapeutic indications or treatments not previously disclosed

Given the broad nature of PCT applications, the scope covers not just the compound itself but also its plausible formulations and therapeutic methods.


Claims Analysis

Overview of Claims

The claims constitute the legal core of the patent, outlining the scope of protection. They can be categorized into independent claims, which define the broad inventive concept, and dependent claims, which specify preferred embodiments, particular formulations, or usage methods.

Independent Claims

Typically, a patent like WO03061744 features one or more independent claims directed at:

  • The chemical compound itself (e.g., a specific molecular structure).
  • Pharmaceutical compositions containing the compound.
  • Methods of treating particular diseases or conditions using the compound.

The breadth of these claims determines the patent's enforceability and the scope of exclusivity granted.

Claim Specificity and Novelty

  • Structural Features: Claims likely specify unique substituents, stereochemistry, or molecular frameworks that distinguish the compound from prior art.
  • Formulation Claims: Claims may describe formulations with specific excipients or delivery systems designed to optimize therapeutic outcomes.
  • Method of Use Claims: These specify particular medical indications, dosages, or treatment protocols linked to the compound.

The strength of these claims depends on their novelty over existing prior art. Any overlapping prior art could narrow or challenge the scope during patent prosecution or infringement proceedings.

Claim Limitations and Strategies

  • Narrow claims focus on specific compounds or methods, offering higher certainty of validity.
  • Broad claims encompass a wider class of compounds or uses but risk prior art rejections.

Given the typical strategy in pharmaceutical patents, WO03061744 may balance between broad claims to prevent competitors' entry and narrower claims to ensure enforceability.


Patent Landscape Context

Competitive Patent Families

WO03061744 exists within a patent landscape that likely includes:

  • Priority Filings: Earlier patent applications referencing the same invention or similar compounds.
  • Family Members: Corresponding patents filed in key markets such as the US, EU, Japan, etc.
  • Follow-up Applications: Future patents claiming improvements, new indications, or delivery methods.

Patent family analysis reveals how the patent owner plans to maintain strategic exclusivity and defend against competitors.

Prior Art and Patent Citations

  • Prior Art References: Examiners commonly cite prior art references—publications, patents, or scientific articles—during prosecution.
  • Citations: The number and nature of citations of WO03061744 indicate its influence and standing within the patent ecosystem.

A high number of citations suggests a significant technological contribution, whereas fewer citations may indicate a narrower scope or limited novelty.

Potential Challenges and Limitations

  • Obviousness over prior art may threaten validity if the claimed invention is seen as an incremental modification.
  • Restrictive claims may limit commercial utility but strengthen enforceability.
  • Patentability challenges could arise if similar compounds or formulations are disclosed elsewhere.

Legal Status and Expiry

Patent term generally spans 20 years from the priority date, subject to maintenance and annuity payments. The patent's current legal status—granted, pending, or invalidated—substantially impacts its enforceability.


Implications for Stakeholders

Pharmaceutical Innovators

Patent WO03061744 underscores a strategic barrier against generic competition, especially if granted across multiple jurisdictions. Its scope could impede similar compounds or formulations, provided its claims are broad and well-supported.

Patent Strategies

  • Boundary Setting: Clear, well-supported claims maximize legal protection.
  • Continued Innovation: Filing follow-up patents can extend market exclusivity.
  • Landscape Monitoring: Observing citations and related patents aids in assessing freedom-to-operate and potential challenges.

Regulatory and Commercial Outlook

Patents impact regulatory approval pathways by establishing exclusivity and preventing market entry of generics. The broader the patent's scope, the more significant its influence on licensing deals and partnership opportunities.


Key Takeaways

  • Scope and Claims: WO03061744 likely covers specific chemical entities, formulations, and methods of use, with strength determined by claim novelty and breadth.
  • Patent Landscape: The patent exists within a dense ecosystem of related patent families, with potential citations indicating its influence and strategic importance.
  • Legal Strategy: Clear, inventive claims and comprehensive prosecution across jurisdictions bolster commercial exclusivity.
  • Market Impact: Securing broad and enforceable patent rights deters competition, enabling strong market positioning.
  • Patent Lifecycle: Continuous monitoring of status, citations, and related applications is essential for maintaining competitive advantage.

FAQs

1. What is the primary focus of WIPO patent WO03061744?
The patent concentrates on a novel pharmaceutical compound, its formulations, or therapeutic methods, aimed at treating specific medical conditions.

2. How broad are the claims typically in WO03061744?
The claims likely range from broad chemical structures to specific formulations or use cases, with the breadth depending on patent prosecution and prior art considerations.

3. Can WO03061744 be enforced internationally?
Yes, through national phases in jurisdictions where it is granted. Its enforceability depends on successful prosecution and validity in each jurisdiction.

4. How does this patent fit into the overall drug patent landscape?
It represents a strategic innovation that potentially blocks competitors and enables market exclusivity, especially when combined with subsequent patent families and follow-up applications.

5. What are potential challenges to WO03061744's validity?
Prior art disclosures, obviousness, or lack of novelty could threaten its validity, especially if similar compounds or formulations exist in existing literature.


References

  1. World Intellectual Property Organization. (2003). WO03061744. Patent Application.
  2. WIPO PATENTSCOPE. Global Patent Dataset.
  3. Patent Office Records and Literature Analysis Reports.

(Note: Specific linkages to public databases and patent documents should be consulted for actual patent statuses and detailed claims.)

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