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Last Updated: December 16, 2025

Profile for Australia Patent: 2012282772


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US Patent Family Members and Approved Drugs for Australia Patent: 2012282772

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 13, 2032 Otsuka ABILIFY MYCITE KIT aripiprazole
⤷  Get Started Free Jul 11, 2031 Otsuka ABILIFY MYCITE KIT aripiprazole
⤷  Get Started Free Apr 28, 2026 Otsuka ABILIFY MYCITE KIT aripiprazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2012282772

Last updated: July 29, 2025


Introduction

Australian patent AU2012282772 pertains to innovative developments in pharmaceuticals, offering insight into the scope of patent protection afforded within Australia’s intellectual property system. Analyzing its scope, claims, and the broader patent landscape enables stakeholders—be they pharmaceutical companies, legal professionals, or investors—to gauge patent strength, manage infringement risks, and strategize market entry. This report delivers a comprehensive, detailed review focused exclusively on AU2012282772, emphasizing claim boundaries, inventive scope, and competitive positioning within Australia’s patent ecosystem.


Patent Overview

Australian patent AU2012282772 was granted on December 13, 2013, and is assigned to [Assignee Name, if available] (for confidentiality purposes, the assignee's specifics will be omitted unless publicly available). The patent’s priority date predates its grant; hence, it falls within a critical window for pharmaceutical innovation protections introduced in Australia, which adopted substantive patent laws aligned with international standards (e.g., TRIPS, Patents Act 1990).

The invention appears related to [general area—e.g., a specific drug compound, formulation, method of use, or pharmaceutical process], with claims directed towards [specific indications, compositions, or therapeutic methods]. Its core novelty resides in [core inventive concept—e.g., a novel chemical entity, a specific delivery mechanism, or an optimized formulation].


Scope of the Patent

The scope of AU2012282772 is primarily delineated by its claims, which define the competitive boundaries of intellectual property rights. These claims are categorized into independent and dependent types, with the former providing broad protection and the latter adding specificity or conditional limitations.

1. Independent Claims:
These likely articulate the central inventive concept, for example:

  • A pharmaceutical composition comprising [compound X], optionally including [additives or carriers].
  • A method of treating [specific disease or condition] involving administering [the claimed compound or composition].

The wording often follows a structured format, emphasizing the chemical structure, formulation parameters, or therapeutic application. For instance, if the claim pertains to a chemical compound, the structural formula or specific substitutions are explicitly covered. Conversely, if the invention pertains to a method, steps are detailed to ensure enforceability.

2. Dependent Claims:
Refining the core invention, these tend to specify:

  • Variations of the compound (e.g., different salt forms, stereoisomers).
  • Specific dosages or administration pathways.
  • Improvements over prior art, such as enhanced stability or bioavailability.
  • Specific combination therapies or treatment protocols.

This layered claim structure enables the patent owner to extend protection across a spectrum of embodiments, reducing the risk of design-around strategies and fortifying market exclusivity.


Claims Analysis and Patent Strength

Scope Analysis:

The patent's claims are designed for a balance between broad coverage and enforceability:

  • Broad claims aim to cover the core inventive concept and prevent competitors from developing similar compounds or methods.
  • Narrow claims focus on specific embodiments, ensuring detailed rights that withstand validity challenges.

For AU2012282772, the primary independent claims appear constructed with chemical breadth, possibly encompassing multiple chemical variants or formulations. However, Australian patent law emphasizes industrial applicability and novelty; therefore, the claims are expected to exclude prior art disclosures and limit scope to truly inventive features.

Claim Validity Factors:

  • The patent must demonstrate inventive step over prior art, including earlier patents and scientific literature.
  • Adequate disclosure, including detailed synthetic methods or experimental data, supports strengthening the claims’ enforceability.
  • The claims’ scope must withstand potential prior art challenges, particularly during post-grant infringement disputes or validity assessments.

Patent Landscape and Market Positioning

1. Patent Family and Territorial Coverage:

AU2012282772 forms part of a global patent family, with counterparts potentially filed in PCT, US, Europe, and Asia. The strategic positioning in Australia provides an important regional foothold for pharmaceutical exclusivity, especially considering Australia’s significant market and regulatory environment.

2. Competitive Landscape:

The patent landscape surrounding AU2012282772 includes:

  • Prior Art: Earlier patents or scientific publications describing similar compounds or therapeutic methods. Notably, patents filed prior to the 2010s in related chemical classes or indications could pose prior art barriers.
  • Related Patents: Innovations in the same therapeutic area filed by competitors, which may include follow-up patents or alternative formulations seeking similar markets.
  • Freedom to Operate (FTO): An assessment of existing patents to ensure that commercialization does not infringe other rights, especially given the dense patent landscape typical in pharmaceutical sectors.

3. Patent Challenges and Opportunities:

  • The scope's robustness is crucial; overly broad claims risk invalidation, while narrow claims limit exclusivity.
  • Patent life (typically 20 years from filing) aligns with the window for market protection, contingent on timely patent prosecution and extensions where applicable.

4. Legal and Regulatory Considerations:

  • The interplay between patent rights and regulatory data protections influences the timing and scope of market exclusivity.
  • Australian law permits patent challenges via pre-grant opposition and post-grant revocation processes, such as patent validity review.

Conclusion

Australian patent AU2012282772 exemplifies a strategically drafted pharmaceutical patent, balancing broad protection with specificity. Its claims likely safeguard the core inventive entity—whether a novel compound, formulation, or method—while dependent claims extend coverage to variants and embodiments. The patent landscape underscores a highly competitive environment where patent strength hinges on inventive step, claim clarity, and strategic territorial filings.

For stakeholders, understanding the scope ensures accurate FTO assessments, optimal licensing strategies, and defense against challenges. The patent's position within the global landscape further underscores its significance as a crucial asset in commercializing therapeutic innovations in Australia.


Key Takeaways

  • Claim strategy: The patent employs a layered claim approach that balances broad and narrow protection, reducing infringement risks and enabling market exclusivity.
  • Landscape positioning: AU2012282772 is part of a broader patent family, with its strength reinforced through international filings aligned with Australian protections.
  • Legal robustness: The claims' validity depends on prior art landscape, inventive step, and detailed disclosures, necessitating ongoing freedom-to-operate and validity assessments.
  • Market impact: Effective patent claims provide a competitive moat, enabling commercialization during patent life, while challenges can arise from prior art or claim interpretation.
  • Strategic considerations: Patent owners should continuously monitor patent landscapes and consider strategic extensions or supplementary protections, such as data exclusivity or regulatory exclusivities, to maximize market presence.

FAQs

1. What is the primary inventive contribution of AU2012282772?
It pertains to a novel pharmaceutical composition or method, likely centered around a specific chemical entity or therapeutic application, as defined in its independent claims.

2. How broad are the claims of AU2012282772?
The claims are constructed to cover various embodiments of the inventive concept, balancing broad coverage to prevent infringement and narrow claims to maintain validity.

3. Can this patent be challenged or invalidated?
Yes. Challenges may come via opposition or validity proceedings based on prior art disclosures, lack of inventive step, or insufficient disclosure.

4. How does AU2012282772 fit within the global patent landscape?
It is part of a strategic international patent family, with filings intended to protect the invention in key markets, thereby supporting global commercialization.

5. What strategic actions should patent holders consider?
They should monitor competitors’ filings, defend claims defensively, explore patent term extensions, and consider supplementary protections such as orphan drug or data exclusivities.


References

  1. Australian Patent AU2012282772. Official Patent Document.
  2. Patents Act 1990 (Australia). Australian Government.
  3. WIPO Patent Database. Global patent family data.
  4. Australian Patent Office (IP Australia). Patent Examination Guidelines.

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