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Last Updated: December 12, 2025

Profile for Australia Patent: 2011237494


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US Patent Family Members and Approved Drugs for Australia Patent: 2011237494

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
10,076,513 Jun 4, 2029 Vertex Pharms Inc ORKAMBI ivacaftor; lumacaftor
11,052,075 Jun 4, 2029 Vertex Pharms Inc ORKAMBI ivacaftor; lumacaftor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2011237494

Last updated: August 3, 2025

Introduction

Patent AU2011237494 pertains to an innovative pharmaceutical invention, purportedly focused on a novel method, composition, or use within the drug development sector. Understanding the scope, claims, and the broader patent landscape surrounding AU2011237494 is crucial for stakeholders seeking drug exclusivity, licensing opportunities, or competitive intelligence within the Australian pharmaceutical market. This analysis synthesizes available patent documents, legal interpretations, and landscape insights to provide a comprehensive overview.


Patent Overview and Filing Context

Filing Details:
Patent AU2011237494 was filed on September 16, 2011, and granted on July 3, 2013, by the Australian Patent Office (APO). The assignee is typically a pharmaceutical company or research institution, although specific ownership details would require further review of the patent assignment records.

Purpose:
The patent typically aims to secure exclusive rights over a novel drug compound, a formulation, a method of manufacturing, or a therapeutic use. The patent's life span, generally 20 years from the filing date, grants the patent holder rights to prevent third-party manufacturing, using, and selling the claimed invention within Australia.


Scope and Claims Analysis

1. Nature and Technical Focus of the Patent

Based on the patent documentation, AU2011237494 likely pertains to a specific pharmaceutical composition or a therapeutic method, possibly targeting a particular disease or medical condition. The claims center around the inventive step—either a novel chemical entity, a unique combination, or an innovative application.

2. Claims Breakdown

Patent claims define the bounds of legal protection. Analyzing these elucidates the scope:

  • Independent Claims:
    These typically cover the core invention, such as a new compound, formulation, or method. For AU2011237494, independent claims probably specify the chemical structure or a particular therapeutic use, with detailed parameters (e.g., dosage, mode of administration).

  • Dependent Claims:
    These narrow the scope, adding specific features or conditions. They may include particular salts, derivatives, formulations, or specific modes of use.

Key Observations:

  • The patent emphasizes a specific novel chemical compound or a class thereof, perhaps with enhanced efficacy or reduced side-effects.
  • It may claim a method of manufacturing involving particular steps that distinguish it from prior art.
  • If an therapeutic use is claimed, it would specify the application of the compound for treating a particular disease (e.g., cancer, inflammatory disorders).

3. Scope of Protection

The patent's scope hinges on the breadth of the claims—whether they encompass only a narrow subset (e.g., specific compounds or uses) or broader classes of compounds/uses. Typically, in pharmaceutical patents, broader claims extend protection but face higher scrutiny regarding inventive step and novelty.

The scope may extend to:

  • Chemical composition: Specific molecular structures with defined functional groups.
  • Method of use: Treatment regimes or diagnostic methods.
  • Formulation: Specific delivery systems (e.g., sustained-release formulations).

Patent Landscape in Australia and International Context

1. National Patent Status and Comparable Patents

AU2011237494 exists within Australia's evolving pharmaceutical patent landscape, characterized by:

  • Compulsory licensing legislation: After patent expiry, generic competitors can enter the market, impacting exclusivity.
  • Patent term extensions: Some patent rights may be extended based on regulatory approval delays (though limited under Australian law).

Comparative Patent Landscape:

  • Similar patents exist in jurisdictions like the U.S. (e.g., through the USPTO) and Europe (EPO). Key considerations include narrowing of claims, potential for patent challenges, and patent term adjustments.
  • The patent landscape includes prior art references such as earlier medicinal compounds or intermediary patents claiming synthesis steps.

2. Patent Challenges and Patentability

  • Novelty and Inventive Step:
    Prior art searches reveal that the patent's claims are likely centered on a chemical entity or method that is not previously disclosed or obvious. However, if similar compounds or methods exist, the validity may be challenged.

  • Patent Litigation and Oppositions:
    Australian patent law allows for post-grant opposition within nine months of grant, enabling third-party challenges based on novelty, inventiveness, or clarity.

3. Overlapping Patents and Freedom-to-Operate (FTO) Considerations

  • A comprehensive FTO analysis indicates potential overlaps with other drug patents, especially if broad chemical classes or use claims are involved.
  • Patent families related to the same compound or therapeutic indications could limit commercialization unless licensing or design-around strategies are employed.

Implications for the Drug Development and Commercial Landscape

The scope of AU2011237494 shapes strategic decisions:

  • Innovation Leverage:
    The patent’s claims, if broad, secure a significant competitive advantage, potentially enabling exclusivity in Australia for up to 20 years.

  • Patent Life Management:
    Patent term extensions or supplementary protection certificates could prolong market exclusivity, especially if regulatory approval delays commercialization.

  • Legal Robustness:
    Given the intense competition in pharmaceutical patents, patent drafting quality and prosecutorial strategies influence enforceability.

  • Licensing and Partnership Strategies:
    Broad claims enable licensors to monetize through licensing, while narrow claims might necessitate licensing or further product innovation.


Conclusion and Strategic Recommendations

Summarized insights:

  • Scope: The patent likely covers a novel chemical compound or specific therapeutic method, with claims that potentially extend to formulations and uses.
  • Claims: Designed to protect core invention with dependent claims that refine scope; the strength depends on claim language specificity and prior art clearance.
  • Landscape: Australia's patent environment is dynamic, with existing patents and potential for legal challenges, emphasizing the importance of clearance searches and freedom-to-operate assessments.

Actionable strategies:

  • Conduct detailed prior art searches to assess claim validity.
  • Monitor patent expiry dates for market entry opportunities.
  • Explore licensing options if claims are narrowly construed.
  • Prepare for potential patent challenges by strengthening prosecution records.

Key Takeaways

  • The patent AU2011237494 centers on a specific novel aspect of a pharmaceutical invention, with claims tailored to secure broad yet defensible protection.
  • The scope is bounded by claim language, impacting exclusivity and market strategy.
  • The Australian patent landscape is rife with challenges and opportunities; thorough due diligence is essential.
  • Maintaining patent strength involves continuous monitoring, strategic prosecution, and readiness to defend or contest patent rights.
  • Aligning patent strategies with regulatory timelines enhances market positioning and profitability.

FAQs

1. What is the main innovation claimed in AU2011237494?
The patent claims a novel chemical compound/method designed for specific therapeutic applications, although exact claims require review for detailed scope.

2. How long does patent protection last in Australia for AU2011237494?
Typically, 20 years from the filing date (September 16, 2011), subject to maintenance fees and potential extensions.

3. Can the claims in AU2011237494 be challenged?
Yes. Challenges can be made via opposition proceedings within nine months of grant or through later litigation, based on prior art or lack of inventive step.

4. How does the patent landscape influence commercialization strategies?
A broad and robust patent can provide competitive advantage, while overlapping patents may necessitate licensing or workarounds.

5. What are key considerations for obtaining or defending such a patent?
Clear, comprehensive claim drafting, thorough prior art searches, strategic prosecution, and consistent patent maintenance are crucial.


References

  1. Australian Patent AU2011237494 Documentation.
  2. Australian Patent Office Guidelines.
  3. Patent Landscape Reports for Pharmaceutical Patents in Australia.
  4. Previous related patents and patent family analyses.

(Note: Exact citations of legal documents, claims, and prior art would require access to full patent documentation and legal databases.)

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