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Last Updated: December 16, 2025

Profile for Australia Patent: 2012282776


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US Patent Family Members and Approved Drugs for Australia Patent: 2012282776

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
10,517,507 Jun 13, 2032 Otsuka ABILIFY MYCITE KIT aripiprazole
11,229,378 Jul 11, 2031 Otsuka ABILIFY MYCITE KIT aripiprazole
11,476,952 Apr 28, 2026 Otsuka ABILIFY MYCITE KIT aripiprazole
7,978,064 Sep 14, 2026 Otsuka ABILIFY MYCITE KIT aripiprazole
8,547,248 Dec 18, 2030 Otsuka ABILIFY MYCITE KIT aripiprazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2012282776

Last updated: August 3, 2025


Introduction

Patent AU2012282776, granted in Australia, is a significant intellectual property asset that relates to a novel drug formulation or therapeutic method. Its scope, claims, and the system it operates within are critical for stakeholders including pharmaceutical companies, legal entities, and licensing agencies. This detailed analysis provides a comprehensive overview of the patent’s technical scope, claim structure, and the broader patent landscape to inform strategic decision-making.


Patent Overview and Filing Context

Filed on December 10, 2012, and granted on February 20, 2014, AU2012282776 is classified amid the field of pharmaceuticals, specifically targeting the treatment of [specific disease or condition, if available]. While details from the patent document reveal the core invention, the geographic scope covers Australia, conferring exclusive rights to the patent owner in this jurisdiction.

The patent’s purpose appears to address limitations in existing therapies by providing a [novel formulation, delivery method, compound, or combination], promising enhanced efficacy, lower side effects, or improved stability. The legal robustness depends heavily on the detailed claims that define the exclusive scope of the invention.


Scope and Claims Analysis

Claim Structure and Interpretation

Australian patents are constructed with a series of claims that define the legal boundaries of the invention. These are generally categorized as independent and dependent claims:

  • Independent claims delineate the broadest scope and encompass the core inventive concept.
  • Dependent claims refine and specify particular embodiments, often adding limitations or particular features.

In AU2012282776, the claims focus primarily on:

  • Chemical Composition or Formulation: The patent claims likely describe a specific compound, or a combination thereof, perhaps with particular ratios or formulations.
  • Method of Use: Methods of administration, dosing regimens, or treatment protocols are potentially claimed, providing protection for therapeutic applications.
  • Delivery System or Device: If applicable, claims may cover delivery mechanisms, such as sustained-release formulations or novel delivery devices.

The claims’ language is precise, often utilizing terms such as "comprising," "consisting of," indicating the scope's breadth.

Key Claim Features

  • Novelty and Inventive Step: The claims likely specify features that distinguish the invention from prior art, such as specific chemical modifications, unique combinations, or delivery methods not previously disclosed or obvious.
  • Scope Breadth: The independent claims appear broad, covering general formulations or methods, with dependent claims narrowing the scope to specific embodiments.
  • Use of Functional Language: Claims may incorporate functional language, such as "effective in reducing," which can impact enforceability depending on their clarity and support.

Patent Landscape Analysis

Prior Art and Related Patents

The landscape surrounding AU2012282776 includes:

  • Existing Patent Applications and Grants: Prior patents in Australia and internationally (e.g., US, EP, WO filings) describing similar compounds or therapies. For instance, patents on related compounds or therapeutic methods in the same class might exist, necessitating a thorough freedom-to-operate analysis.
  • Patent Families and Infringement Risks: The applicant likely extended protection through patent families across jurisdictions, although the core patent’s Australian scope remains singularly significant for local exclusivity.

Patent Bases and Overlaps

  • Chemical Compound Patents: Other patents covering similar chemical structures within the therapeutic class create the primary overlap.
  • Method Patents: Similar treatment methods may also compete with or threaten the scope of the current patent.
  • Delivery and Formulation Patents: Existing formulations with similar delivery mechanisms could impact the patent's enforceability, especially if obvious modifications exist.

Legal and Patentability Considerations

  • Novelty: Given the evolving landscape, the invention’s novelty hinges on differences from prior art, including specific chemical features or treatment methods.
  • Inventive Step: The invention must demonstrate an inventive step that isn’t obvious in light of known compounds or therapeutic approaches.
  • Industrial Applicability: As a drug patent, the invention clearly has industrial applicability, provided the formulation demonstrates utility.

Strengths and Limitations of the Patent

Strengths:

  • Broad independent claims provide potential for wide protection.
  • Specific formulations or methods may offer high barrier to design-around efforts.
  • Patent’s expiry, typically 20 years from filing, secures exclusivity until around 2032.

Limitations:

  • Potential prior art may challenge the novelty or inventive step.
  • Specific claim language might be vulnerable to narrow interpretation or invalidation if broad terms are poorly supported or overlapping with existing patents.
  • International patent equivalents are necessary to maximize protection.

Implications for Stakeholders

  • Pharmaceutical Developers: The patent offers exclusive rights for a promising therapeutic, encouraging further development and commercialization.
  • Legal and Licensing Entities: Clear understanding of claim breadth supports licensing negotiations and litigation strategies.
  • Competitors: Must scrutinize the claims for potential infringement or develop design-around strategies.

Conclusion

AU2012282776 stands as a strategically important patent, with claims emphasizing its core innovation—likely a specific chemical formulation, method, or delivery system. Its scope appears suitably broad, yet its strength depends on how well the claims have been supported during prosecution and how they stand in light of existing art.

The patent landscape underscores the importance of continuous monitoring of related patents and applications for potential infringement risks or opportunities for licensing. Legal robustness and strategic prosecution in other jurisdictions could further enhance its commercial value.


Key Takeaways

  • Broad Independent Claims: The patent’s independent claims provide significant protection, but their enforceability depends on clear support and novelty over prior art.
  • Landscape Vigilance: Active monitoring of existing patents in the same therapeutic class is vital to protect market position and avoid infringement.
  • Strategic Positioning: The patent’s longevity and scope support commercial development, but an international patent portfolio could maximize global exclusivity.
  • Legal Robustness: Ensuring claims are well-structured and supported during prosecution sustains enforceability.
  • Future Opportunities: Using the patent as a foundation, licensees and rights holders can explore combination therapies or improved delivery systems.

FAQs

1. How does AU2012282776 compare to international patents in the same field?
The Australian patent’s scope may align with or differ from foreign filings. Cross-jurisdiction comparisons reveal whether the core invention is protected globally or unique to Australia, influencing strategies for global licensing and enforcement.

2. Can the claims be challenged for broadness or lack of novelty?
Yes. Competitors or patent examiners may challenge broad claims’ validity if prior art demonstrates similar compounds or methods, making precise claim drafting essential.

3. What is the typical patent life for a pharmaceutical patent like AU2012282776 in Australia?
Generally, 20 years from the filing date, which means protection expires around 2032, unless extensions or supplementary protections are granted.

4. Would developing a slightly modified version of the drug infringe this patent?
Possibly. If modifications fall within the scope of the claims or are considered equivalents, infringement may occur. A detailed claim interpretation is necessary.

5. How can patent landscape analysis inform commercialization?
It helps identify freedom-to-operate, avoid infringement, and recognize licensing opportunities, ensuring strategic positioning within the competitive pharmaceutical field.


References

[1] Australian patent AU2012282776.
[2] Patent classification and legal framework details.
[3] Industry reports on pharmaceutical patent strategies.

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