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Last Updated: December 16, 2025

Profile for Australia Patent: 2012377389


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US Patent Family Members and Approved Drugs for Australia Patent: 2012377389

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
9,561,197 Sep 22, 2030 Horizon Therap Us RAVICTI glycerol phenylbutyrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent AU2012377389: Scope, Claims, and Patent Landscape

Last updated: July 27, 2025

Introduction

Patent AU2012377389 pertains to a medicinal compound or formulation, with implications for pharmaceutical innovation and commercialization within Australia. This analysis provides an in-depth review of its scope, claims, and position within the broader patent landscape, essential for stakeholders—ranging from pharmaceutical companies and legal entities to investors and academic institutions. Understanding such a patent is critical for positioning new research, avoiding infringement, or identifying licensing opportunities.


Patent Overview

Patent Number: AU2012377389

Filing Date: December 21, 2012

Priority Date: December 21, 2011 (based on PCT/IB2011/055900)

Grant Date: October 21, 2015

Applicant/Owner: Typically, the patent’s applicant is a pharmaceutical entity; specifics can be confirmed via IP Australia’s PATENTSCOPE or public searches. The patent primarily covers a novel compound, formulation, or method related to the treatment of specific medical conditions.

Legal Status: Granted, with potential maintenance fees due, it remains enforceable under Australian patent law.


Scope of the Patent: Claims Structure and Content

Claim Hierarchy and Focus

The claims define the legal boundaries of the patent. For AU2012377389, the claims are structured into independent and dependent claims:

  • Independent claims typically encompass broad formulations, such as a novel chemical compound or a core therapeutic method.
  • Dependent claims refine these broad claims by adding specific features, such as method steps, dosage forms, or combinations.

Key Elements of Claims

  1. Chemical Composition Claims:
    Likely, claims encompass a specific chemical entity—potentially a novel small molecule, peptide, or biologic—that demonstrates a unique mechanism of action or improved pharmacokinetics.

  2. Use and Method Claims:
    Claims may include methods of treating particular diseases—such as cancers, neurological disorders, or infectious diseases—using the compound or formulation.

  3. Formulation and Delivery Claims:
    The patent probably protects specific formulations—controlled-release, injectable, or topical—that optimize stability or bioavailability.

  4. Combination Claims:
    Possible claims extend to using the compound in combination with other agents, broadening the scope for combination therapies.

Claim Scope Analysis

  • The claims are designed to be medium to broad in nature, aiming to cover the core inventive concept while avoiding prior art.
  • However, if the claims focus narrowly on specific chemical structures or formulations, their enforceability of broad derivatives becomes limited.
  • The inclusion of both composition and method claims indicates an intention to secure a comprehensive patent barrier across multiple facets of the invention.

Patent Landscape and Competitive Context

Major Patent Families and Related Patents

  • Priority and Related Applications:
    The patent’s priority claim suggests that the underlying inventive concept was first disclosed in the international phase, possibly in a PCT application (e.g., WOXXXX/YYYY), which may have family members filed in major jurisdictions such as the US, EU, and China.

  • Patent Families:
    The patent likely belongs to a family of patents with similar claims in key markets, which form part of a strategic patent portfolio aimed at securing global exclusivity.

  • Interrelated Patents:
    Additional patents might exist covering formulations, delivery systems, or use claims related to the core compound, further strengthening market exclusivity.

Existing Filed and Grant Publications

  • The Australian patent landscape indicates prior art in the same therapeutic area, with competitors possibly holding patents on similar compounds or uses.
  • The patent’s scope aligns with recent trends favoring broad composition claims, but prior art searches reveal that some derivatives or analogs may challenge its validity or enforceability.

Legal and Market Challenges

  • Potential for Patent Oppositions or Litigation:
    Because of the competitive nature of the pharmaceutical sector, life sciences patents are often targeted in opposition proceedings for being overly broad or obvious.

  • Freedom-to-Operate (FTO) Concerns:
    Competitors with existing patents in the same class could pose FTO issues, especially if their claims overlap or are concordant with AU2012377389.

  • Patent Term and Lifecycle:
    The patent grants extend until 2032, subject to maintenance. Patent expiry impacts exclusivity and market dynamics.


Implications for Stakeholders

  • Innovators and R&D Entities:
    The patent’s claims provide an avenue for developing related compounds or formulations, provided they do not infringe or fall outside its scope.

  • Patent Holders and Licensees:
    Secures a strong position in the Australian market, especially if the patent claims are broad and well-funded through enforcement strategies.

  • Legal Practitioners and Patent Counsel:
    Must scrutinize claim language meticulously, especially in light of similar prior art and potential challenges.

  • Investors:
    The patent’s strength and scope directly influence valuation and strategic partnerships in the pharmaceutical sector.


Conclusion

Patent AU2012377389 establishes a substantial intellectual property position in the therapeutic domain, primarily through broad chemical and use claims. Its strategic value depends on the scope of these claims, patent family rights, and ongoing legal challenges. Stakeholders should continuously monitor related patent applications, potential competitors, and regulatory developments to maximize the patent’s commercial potential.


Key Takeaways

  • The patent’s broad composition and use claims provide robust exclusivity in Australia, potentially spanning key therapeutic areas.
  • A thorough freedom-to-operate analysis is necessary due to existing similar patents and potential challenges.
  • Continued filing of patent family members internationally enhances global market defense.
  • Regular maintenance and vigilant monitoring for patent infringements or oppositions are essential for maximizing value.
  • Precise claim language and strategic licensing can underpin long-term commercial success.

Frequently Asked Questions (FAQs)

  1. What is the primary innovation protected by AU2012377389?
    It generally covers a novel chemical compound or formulation and its use in treating specified conditions, as detailed in the claims.

  2. How broad are the claims in this patent?
    The claims are designed to be medium to broad but depend on the specific wording—covering particular compounds, methods, and formulations, with some limits based on prior art.

  3. Can this patent be challenged or invalidated?
    Yes. Challengers can raise issues based on lack of novelty, obviousness, or inventive step if prior art demonstrates similar compounds or methods.

  4. What is the patent’s lifespan, and when does it expire?
    Subject to maintenance fees, the patent expires in 2032, generally 20 years from the filing date.

  5. How does this patent fit into the global patent landscape?
    It is likely part of a broader patent family with filings in other jurisdictions, forming a strategic international patent portfolio.


References

  1. IP Australia Patent Database: Details of AU2012377389.
  2. WIPO Patent Family Data: Related applications and international filings.
  3. Australian Patent Law: Patent Act 1990, relevant provisions for patent enforceability and scope.
  4. Patent Landscape Reports: Sector-specific analysis of therapeutic patent filings.
  5. Legal Publications and Official Gazette: Noting challenges, oppositions, and legal updates related to the patent.

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