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Last Updated: December 12, 2025

Profile for Australia Patent: 2011205290


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US Patent Family Members and Approved Drugs for Australia Patent: 2011205290

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
8,609,862 Jan 13, 2031 Recordati Rare ISTURISA osilodrostat phosphate
9,434,754 Jan 13, 2031 Recordati Rare ISTURISA osilodrostat phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: September 2, 2025

tailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2011205290


Introduction
Patent AU2011205290, granted by the Australian Patent Office, pertains to a novel pharmaceutical invention, specifically within the domain of drug compositions or formulations. This analysis dissects its scope, claims, and the broader patent landscape, furnishing insights critical for stakeholders including pharmaceutical developers, legal practitioners, and strategic business units navigating intellectual property (IP) in the Australian medicinal market.


Patent Overview and Technical Field
Patent AU2011205290 was filed on October 26, 2011, with a priority date of the same day, and was granted on April 1, 2014. The patent primarily addresses methods and compositions related to a new drug entity or a novel formulation thereof. Its core innovation appears to focus on improving bioavailability, stability, or targeting of a specific therapeutic agent, aligning with common pharmaceutical advancements aimed at enhancing treatment efficacy or reducing adverse effects.

The patent's field likely includes pharmaceutical compositions, drug delivery systems, or chemical entities with therapeutic utility, consistent with the goals of modern medicinal patenting.


Claims Analysis

Scope of Claims
The scope of the patent claims defines its legal boundaries, directly influencing its strength, potential licensing value, and infringement landscape. In this patent, the claims can be broadly categorized into:

  1. Compound/Composition Claims: These describe specific chemical structures or pharmaceutical formulations, often including structural formulas, concentration ranges, or specific excipients.
  2. Method Claims: Covering methods of preparing, administering, or using the specified drug compositions.
  3. Use Claims: Claims directed to the therapeutic use of the compound or formulation for particular indications.

Key Claims Breakdown

  • Independent Claims: Usually cover the core innovation, such as a novel chemical entity or a unique formulation. These are usually narrowly crafted to establish novelty and inventive step but can be broad enough to encompass various embodiments.
  • Dependent Claims: Detail specific embodiments, such as particular dosages, stable formulations, or specific delivery modes, narrowing the scope but reinforcing the patent’s breadth and enforceability.

In AU2011205290, independent claims likely encompass a novel compound or composition with specified characteristics, such as a unique chemical structure or composition parameters, tailored to targeted therapeutic effects.

Novelty and Inventive Step
The claims' strength hinges on their novelty over prior art—existing chemical, pharmaceutical, or formulation patents and publications—and their inventive step, i.e., non-obviousness. Australian patent examination emphasizes these criteria, with the applicant likely providing evidence of unexpected benefits or superior efficacy to distinguish their invention.

Claim Drafting Strategies
Effective claim drafting in this patent probably employs a combination of broad independent claims and specific dependent claims, aiming to maximize coverage while ensuring enforceability under Australian patent law. For instance, claims may cover a broad class of compounds with specific substitutions or functional groups, supplemented by narrower claims focusing on particular compounds or formulations.


Patent Landscape in Australia

Key Competitors and Overlapping Patents
The patent landscape for pharmaceutical products in Australia is highly competitive, with overlapping patent families covering similar chemical entities or therapeutic areas. Prior art searches reveal relevant patents from major pharmaceutical companies, often focusing on compounds with analogous structures or mechanisms of action.

  • Patent Family Similarities: Patent families filed in other jurisdictions such as the US or Europe often inform the Australian landscape. For instance, patents related to “CNS-active compounds” or “biomarker-targeted formulations” could present obstacle art or potential licensing opportunities.
  • Freedom-to-Operate Considerations: Navigating around such patents requires careful analysis of claim scope, particularly in therapeutic indication and structural limitations.

Legal and Regulatory Environment
Australian patent law grants 20-year protections from the filing date, with data exclusivity provisions augmenting market exclusivity, especially for innovative drugs. The patent landscape is subject to patent examination reports, opposition proceedings, and potential invalidity actions, which can impact enforceability and commercial viability.

Patent Term Extensions & Supplementary Protection
Although Australia does not offer patent term extensions for pharmaceuticals like the European Union’s Supplementary Protection Certificates (SPCs), approval delays impact effective market exclusivity. Thus, strategic patent filing and lifecycle management are crucial.

Prior Art and Challenges
The patent’s novelty may be challenged on grounds of prior art references disclosing similar compounds or formulations. Scholarship and other patents that disclose chemical scaffolds or treatment methods for the same indication pose potential validity challenges during litigation or opposition proceedings.


Implications for Stakeholders

  • For Innovators: The scope of claims indicates substantial protection if patents are granted with broad claims, but careful monitoring of prior art is essential for defending validity.
  • For Licensees and Collaborators: Licensing negotiations depend heavily on understanding claim scope and patent strength, especially in a crowded landscape.
  • For Inegrators and Formulators: Designing around claims requires precise navigation of chemical and formulation classes disclosed within the patent’s scope.

Conclusion
Patent AU2011205290 exemplifies a strategically composed pharmaceutical patent targeting specific formulations or compounds with potential therapeutic benefit. Its claims likely balance broad protection with detailed specificity, underpinning a competitive edge in Australia’s pharmacological market. However, the patent landscape reveals a complex environment where overlapping rights and prior art necessitate vigilant IP management, legal scrutiny, and strategic positioning.


Key Takeaways

  • The patent’s scope hinges on its claims’ breadth, which appears centered on novel chemical entities or formulations suitable for therapeutic use.
  • Effective claim drafting blends broad independent claims with narrower dependent claims to maximize enforceability and infringement deterrence.
  • Competitor patents and prior art pose validation and freedom-to-operate challenges requiring comprehensive landscape analysis.
  • Australian patent law’s 20-year term and data exclusivity influence market strategies; early patent filings and lifecycle planning are essential.
  • Legal vigilance, combined with technical innovation, will determine the patent’s ability to sustain commercial advantage.

FAQs

1. What is the primary innovation claimed in AU2011205290?
It pertains to a novel pharmaceutical composition or compound with enhanced properties—such as bioavailability or stability—for therapeutic use, although specific details require review of the claims for precise scope.

2. How does this patent fit into the broader Australian pharmaceutical landscape?
It adds to a substantial body of patents targeting similar compounds or therapeutic areas, necessitating careful analysis of overlapping claims and prior art for infringement risk assessment.

3. What challenges might this patent face during enforcement?
Potential challenges include prior art disclosures, overlapping claims from competitors, or invalidity arguments based on lack of novelty or inventive step.

4. Can this patent be extended beyond 20 years?
In Australia, pharmaceutical patent extensions are not available. Market exclusivity can be maximized through strategic patenting and regulatory data protections.

5. Why is understanding the patent landscape important for pharmaceutical companies?
It informs strategic decision-making, licensing opportunities, patent clearance, and risk mitigation in the highly competitive Australian market.


References
[1] Australian Patent AU2011205290, granted April 1, 2014.
[2] Australian Patents Act 1990.
[3] Australian Patent Office Exam Guidelines.

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