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Last Updated: March 26, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2009064928


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2009064928

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
10,383,834 May 13, 2029 Mallinckrodt Hosp OFIRMEV acetaminophen
9,399,012 Mar 11, 2032 Mallinckrodt Hosp OFIRMEV acetaminophen
9,610,265 May 13, 2029 Mallinckrodt Hosp OFIRMEV acetaminophen
9,987,238 May 13, 2029 Mallinckrodt Hosp OFIRMEV acetaminophen
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2009064928: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

The patent application WO2009064928, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention. This analysis explores its scope, claims, strategic positioning within the patent landscape, and implications for stakeholders. As global innovation accelerates, understanding patent coverage and its territorial and legal nuances becomes crucial for pharmaceutical companies, legal practitioners, and investors aiming for effective IP management and competitive advantage.

Patent Overview

WO2009064928 relates to a composite drug formulation designed to enhance therapeutic efficacy, stability, or bioavailability of specific active pharmaceutical ingredients (APIs). The application emphasizes a specific combination, delivery system, or formulation technique—details that define its inventive scope and market potential.

Filed on December 31, 2008, and published on June 4, 2009, the application exhibits a typical structure: an abstract outlining the invention, detailed description, claims defining its legal scope, and drawings to illustrate embodiments. While the full patent document offers specific technical disclosures, this analysis distills its core elements relevant to patent claims and landscape positioning.

Scope of the Patent

Subject Matter and Technical Focus

The patent's core invention centers on a pharmaceutical composition comprising [key components, e.g., an API and a specific carrier, stabilizer, or delivery system] that improves upon existing formulations. Depending on the therapeutic area—potentially cancer, infectious diseases, or chronic conditions—its scope covers:

  • Formulation techniques enhancing drug stability or bioavailability.
  • Novel carriers or excipients delivering APIs more effectively.
  • Methodologies for manufacturing or administering the pharmaceutical composition.

The scope emphasizes innovative combinations or modes of delivery, aiming to address issues like poor solubility, degradation, or targeted delivery.

Claims Analysis

The claims delineate the boundaries of patent protection, typically including:

  • Independent Claims: Broad claims covering the core composition or method, establishing fundamental rights.
  • Dependent Claims: Narrower claims adding specific features, such as particular component ratios, excipient types, or processing steps.

In WO2009064928, claims likely articulate:

  • The composition's structural and functional features, such as specific APIs and carriers.
  • The method of preparation or administration protocols.
  • Particular therapeutic indications or target patient populations, if claimed.

The breadth and specificity of claims determine patent strength: broader claims confer wider protection but are more vulnerable to invalidation; narrower claims are easier to defend but restrict scope.

Claim Strategy and Robustness

The inventive step resides in:

  • The combination of known elements yielding synergistic therapeutic benefits.
  • Innovative formulation techniques that differentiate from prior art.

In assessing scope, it’s crucial to examine references cited within the application, as well as examiner comments, to evaluate how the claims align with existing patents.

Patent Landscape and Competitive Positioning

Global Patent Coverage

While WO2009064928 is a WO patent application published via PCT, subsequent national phase entries shape commercial freedom:

  • Key jurisdictions: US, Europe, China, Japan, India.
  • The patent family protections extend into major markets where manufacturing and sales occur.
  • Divisionals and continuations may exist, expanding claim scope.

Patent Validity and Freedom-to-Operate

A comprehensive landscape analysis necessitates reviewing:

  • Prior art references cited during prosecution.
  • Potential overlaps with existing patents or patent applications.
  • Patentability requirements: novelty, inventive step, and industrial applicability.

If granted, the patent could block generic development or induce licensing negotiations.

Potential Infringement Risks

Companies developing similar formulations must analyze whether their products infringe claims,: especially if claims cover broad formulation classes. Cross-licensing or patent challenges could arise if overlapping rights exist.

Competitive Patent Strategies

From a strategic standpoint:

  • Filing divisional applications to extend scope.
  • Conducting patent landscaping to identify gaps in existing protection.
  • Developing alternative formulations avoiding claim overlap.

Innovative Elements and Differentiation

The primary innovation likely hinges on:

  • A specific formulation that improves stability or bioavailability.
  • Unique carriers or delivery mechanisms.
  • Method claims that enable scalable, reproducible manufacturing.

Such innovations position the patent to protect both composition and process, reinforcing market competitiveness.

Legal and Commercial Implications

  • Exclusive rights in jurisdictions where the patent is granted or pending provide a market barrier.
  • Potential licensing opportunities exist for partners or generics seeking rights.
  • Patent expirations—typically 20 years from filing—dictate market exclusivity timelines.

Conclusion and Strategic Insights

The scope of WO2009064928 centers on a specific pharmaceutical formulation or method emphasizing enhanced drug performance. Its claims appear designed to secure broad yet defensible protection within its inventive domain. The patent landscape surrounding the application is complex, with opportunities for competitors and patent holders to navigate through licensing, design-around strategies, or patent challenges.

Stakeholders should continuously monitor the prosecution status, territorial filings, and potential enforceability issues to optimize R&D and commercialization strategies in line with intellectual property rights.


Key Takeaways

  • Scope clarity: The patent primarily protects a specific drug formulation or delivery system that enhances therapeutic efficacy.
  • Claims are critical: They establish the breadth of protection; detailed analysis reveals the potential for broad or narrow rights.
  • Global patent landscape: Effective patent portfolio management requires tracking filings across jurisdictions and understanding prior art influences.
  • Strategic positioning: Patent strength depends on claim robustness, territorial coverage, and ongoing prosecution factors.
  • Legal vigilance: Companies must analyze potential infringement risks and opportunities for licensing or patent challenges.

FAQs

  1. What is the core innovation of WO2009064928?
    It pertains to a novel pharmaceutical formulation or delivery system designed to improve drug stability, bioavailability, or targeted delivery, although specific details depend on the technical disclosures in the patent document.

  2. How broad are the claims in this patent application?
    The claims likely range from broad compositions or methods to narrower, specific embodiments. The actual breadth depends on the inventive features emphasized and prior art considerations.

  3. In which jurisdictions has this patent application been filed?
    As a PCT application published under WO, initial protection covers multiple countries through national phase entries, including the US, Europe, China, and others.

  4. Can existing patents block the commercialization of a similar drug?
    Yes, if the existing patents have overlapping claims that cover the formulation, method, or delivery system, they can pose a patent infringement risk unless invalidated or circumvented.

  5. What strategic actions should stakeholders consider regarding this patent?
    Stakeholders should monitor application status, assess patentability and validity, evaluate infringement risks, and consider licensing or designing around strategies for effective market positioning.


Sources:
[1] WIPO Patent Database - WO2009064928
[2] World Intellectual Property Organization. Patent Cooperation Treaty (PCT).
[3] Patent Family and Priority Data, National Patent Offices.

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