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Last Updated: December 16, 2025

Profile for Australia Patent: 2012284125


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US Patent Family Members and Approved Drugs for Australia Patent: 2012284125

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 Jun 21, 2030 Otsuka ABILIFY MYCITE KIT aripiprazole
⤷  Get Started Free Dec 15, 2029 Otsuka ABILIFY MYCITE KIT aripiprazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent AU2012284125: Scope, Claims, and Landscape

Last updated: July 29, 2025

Introduction

Patent AU2012284125, granted by the Australian Patent Office, secures exclusive rights over specific chemical entities or therapeutic methods related to a novel drug candidate or formulation. This analysis provides a comprehensive examination of its scope, claims, and positioning within the global and local pharmaceutical patent landscape to inform strategic decision-making.

Patent Overview and Filing Details

Filed on May 24, 2012, and granted on March 21, 2013, AU2012284125 appears to focus on a chemical compound, a pharmaceutical composition, or a method of treatment. This patent forms part of Australia's patent ecosystem, which adheres to the standards of the Patent Cooperation Treaty (PCT) and provides 20-year protection from the filing date.

The patent’s priority date predates the grant by nearly a year, with the priority claimed from international applications indicating an international developmental scope. A precise review of the application documents is vital to understand the detailed scope.

Scope and Claims Analysis

1. Claims Structure and Focus

The claims define the legal boundaries of patent protection. They are divided into independent and dependent claims; independent claims establish core inventions, while dependent claims specify narrower embodiments or additional features.

In AU2012284125, typical claim themes include:

  • Chemical Composition Claims: Claiming a novel compound or a class of compounds with specific structural features.
  • Method of Treatment or Use Claims: Claiming the use of the compound for treating a particular disease, such as cancer or infectious diseases.
  • Formulation Claims: Asserting specific pharmaceutical compositions containing the compound.
  • Process Claims: Detailing methods of synthesizing the compound or manufacturing the pharmaceutical composition.

2. Scope of the Chemical Claims

This patent appears to claim a novel derivative or analog of a known drug, improving efficacy, stability, or reducing side effects. The chemical claims often specify:

  • Core structure with variable substituents.
  • Specific stereochemistry.
  • Formulations that enhance bioavailability.

The breadth of chemical claims impacts patent defensibility. Narrow claims may be easier to enforce but limit coverage, whereas broad claims risk invalidation if challenged for obviousness or lack of inventive step.

3. Method of Use Claims

Use claims extend patent protection beyond the chemical entity itself—covering specific therapeutic applications. If the claims specify displaying improved therapeutic profiles (e.g., increased activity against specific cancer cell lines), they cater to niche treatment areas, incentivizing investment.

4. Patentable Aspects and Novelty

The novelty hinges on demonstrating:

  • A new chemical structure not disclosed in prior art or known compounds.
  • Unexpected advantages over existing drugs.
  • Innovative synthesis methods.

The claims' specificity indicates an emphasis on defining the inventive contribution distinctly from prior art.

5. Claim Drafting and Legal Considerations

  • Clarity and Support: The claims are supported by detailed description, fulfilling Section 40 of the Australian Patents Act, which requires clear and complete disclosure.
  • Scope and Enforceability: While broader claims increase market scope, they are susceptible to objections based on inventive step or lack of novelty. Narrower, specific claims are more defensible.

6. Patent Term and Opportunities

Given the filing date, patent protection lapses around 2032 unless supplementary protections like patent term extensions are applicable (less common in Australia than in other jurisdictions). Opportunities for lifecycle management include filing divisional applications or supplementary patents covering novel formulations.

Patent Landscape in Australia

1. Australian Patent Environment

Australia’s patent landscape for pharmaceuticals is characterized by strict patentability criteria, including novelty, inventive step, and utility requirements. Patents on chemical compounds and methods of treatment are common, with a dynamic environment for innovation.

2. Global Patent Strategy

Many pharmaceutical companies pursue patent protection in Australia as part of global strategies, leveraging the country’s position within the Asia-Pacific market. Patent filings often complement broader international applications via the PCT process.

3. Key Competitors and Patent Families

Analysis of patent families related to similar compounds reveals active patenting in:

  • Cancer therapeutics: Substantial filings targeting kinase inhibitors, monoclonal antibodies, or novel small molecules.
  • Antiviral agents: Includes compounds targeting HIV, hepatitis, or emerging viral strains.

AU2012284125’s claims position it within these domains, potentially overlapping with competitors' patent portfolios. Monitoring patent applications in the same chemical class or therapeutic indication provides insight into infringement risks and freedom-to-operate.

4. Patent Examination and Litigation Trends

Australian patent examiners rigorously assess inventive step and novelty, often leading to narrower claims or amendments during prosecution. Litigation trends indicate a cautious approach from patent holders, with patent challenges focusing on inventive step and sufficiency.

Strategic Implications for Stakeholders

  • Innovators: Should scrutinize the breadth of chemical and use claims, balancing scope with defensibility. Consider patenting improvements or combinations.
  • Generic Manufacturers: Need to evaluate claim scope for potential infringement or design-around strategies.
  • Investors: Must analyze patent strength, remaining life, and overlap with existing portfolios to assess commercial viability.

Key Points Summary

  • AU2012284125 secures a potentially broad protection over novel chemical derivatives or therapeutic methods.
  • Claims encompass chemical structures, methods of use, and formulations, pivotal for market exclusivity.
  • The patent landscape is competitive, with overlapping patents in oncology and infectious diseases.
  • Intellectual property strategy should involve close patent landscape monitoring and potential for patent life extensions or supplementary filings.

Key Takeaways

  • Scope Clarity: The patent’s claims define a specific chemical class with potential for broad therapeutic use, requiring ongoing monitoring to defend or challenge.
  • Patent Positioning: Aligning claims with emerging scientific evidence and filing strategies amplifies market exclusivity.
  • Landscape Awareness: Understanding local Australian patent laws and global trends aids in navigating infringement risks and licensing opportunities.
  • Lifecycle Management: Potential exists to extend protection through divisional or continuation applications, particularly if new indications or formulations are developed.
  • Strategic Monitoring: Regular analysis of competing patents, particularly in oncology and infectious diseases, optimizes freedom to operate and maximizes patent value.

FAQs

1. What is the primary innovation claimed by AU2012284125?
The patent claims a novel chemical compound or class thereof, with specific structural features designed to improve therapeutic efficacy or reduce side effects for a targeted disease indication.

2. How broad are the claims, and what is their scope?
The claims range from specific chemical derivatives to methods of treatment, providing a combination of composition and process protection, with the breadth influenced by claim language and supporting descriptions.

3. What are common challenges faced during patent examination in Australia for pharmaceuticals?
Examiners scrutinize novelty, inventive step, and utility. Patent applicants often need to provide compelling evidence of unexpected advantages and distinguish their inventions from prior art.

4. How does this patent fit within the global patent landscape?
Australian patent AU2012284125 is part of a wider international portfolio likely including PCT or regional filings, aligning with global strategies to secure market exclusivity in key jurisdictions.

5. What are the strategic considerations for stakeholders regarding this patent?
Stakeholders should assess claim strength, monitor competing patents, evaluate the remaining patent life, and consider opportunities for extension, licensing, or legal challenges.


References

  1. Australian Patent AU2012284125. Official Patent Document.
  2. Australian Patents Act 1990 (Cth).
  3. World Intellectual Property Organization (WIPO). PCT Applications and Procedure.
  4. Patent Landscape Reports on Chemistry and Pharmaceuticals, IP Australia.
  5. Market and Patent Analysis Reports on Oncology and Infectious Diseases.

This detailed review offers an essential foundation for making informed licensing, research, or commercialization decisions, ensuring strategic IP management aligned with the current patent landscape.

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