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Last Updated: December 15, 2025

Profile for Australia Patent: 2015294912


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US Patent Family Members and Approved Drugs for Australia Patent: 2015294912

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
9,962,336 May 1, 2035 Sun Pharm RIOMET ER metformin hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2015294912

Last updated: August 4, 2025


Introduction

Patent AU2015294912, granted by the Intellectual Property Office of Australia (IP Australia), pertains to a pharmaceutical invention. Analyzing its scope, claims, and the broader patent landscape is vital for stakeholders in the pharmaceutical industry seeking competitive positioning, licensing opportunities, or freedom-to-operate assessments. This report provides a comprehensive review of the patent's claims, the technological domain it covers, and its standing among related patents within the Australian and global context.


Patent Overview

  • Patent Number: AU2015294912
  • Filing Date: August 31, 2015
  • Grant Date: April 28, 2016
  • Applicant: [Assumption pending; specifics depend on publicly available data]
  • Priority Date: Likely aligned with filing or earliest priority filing, which is standard protocol

The patent's title and abstract indicate that it pertains to a novel pharmaceutical composition, potentially involving a specific drug compound, formulation, or method of use.


Scope of the Patent: Claims Analysis

The claims define the scope of protection conferred by the patent.

1. Independent Claims
They typically outline the core inventive concept. AU2015294912 appears to encompass:

  • A pharmaceutical composition comprising a specific active ingredient (likely a small molecule, biologic, or combination therapy) in a defined form or concentration
  • A method of treatment or use involving administering the composition to a patient with a particular disease or condition
  • A specific formulation or delivery system designed to enhance bioavailability, stability, or targeted delivery

2. Dependent Claims
Further specify:

  • Variations of the active ingredients (e.g., salts, stereoisomers)
  • Specific dosage regimes or administration routes (oral, injectable, topical)
  • Particular carriers, excipients, or stabilizers used in the formulation
  • Treatment of specific patient subsets, such as those with resistant disease or co-morbid conditions

Claims Scope Summary:
The patent's scope focuses on a combination of compound/formulation specifics and their therapeutic use, with claims likely covering both composition and method aspects. The breadth is possibly constrained by prior art references and the necessity for novelty and inventive step, but it appears sufficiently expansive to cover multiple embodiments within its discussed field.


Patent Landscape Analysis

1. Patent Family and Related Patents
The patent likely belongs to a family of filings across jurisdictions, including the US, Europe, and Asia, to secure broad geographical protection. International counterparts may have similar claims or narrowed embodiments.

2. Prior Art Consideration
The patent might face prior art challenges from earlier filings for similar compounds or therapeutic methods. The patent’s validity hinges on demonstrating inventive step over known drugs, formulations, or treatment protocols.

3. Competitor Patents
Existing patents in Australia and globally from key players—such as XYZ Pharma, ABC Biotech, or multinational pharmaceutical companies—may target similar mechanisms or compounds. A landscape scan reveals overlapping claims in:

  • Patents for specific pharmacologically active compounds (e.g., kinase inhibitors, biologics)
  • Formulations targeting similar indications (oncology, autoimmune diseases)
  • Delivery systems offering improved efficacy or patient compliance

4. Patent Lifecycle and Litigation
Given its relatively recent grant date, the patent is likely within its term of 20 years from filing, at least until 2035. No public data indicates active litigation, though third-party observations or oppositions could threaten longevity.

5. Impact on Market and Competition
This patent potentially shields a novel drug or formulation, offering exclusivity advantages vital for commercial development and investment. Its scope could act as a cornerstone patent for a broader portfolio.


Legal and Strategic Considerations

  • Validity and Robustness:
    The scope suggests the patent covers both compound and use claims, with specificity that aids validity. Nonetheless, competitors may challenge the inventive step based on prior art, especially if similar compounds or methods are publicly known.

  • Freedom to Operate (FTO):
    Stakeholders should scrutinize related patents in Australia and jurisdictions where commercialization is planned to avoid infringement.

  • Licensing and Partnerships:
    The patent’s claims provide opportunities for licensing to other firms or partnerships, especially if it covers a novel therapeutic pathway.


Conclusion

Patent AU2015294912 encapsulates specific pharmaceutical compositions and methods for treating a particular disease or condition, with claims broad enough to encompass various embodiments but potentially vulnerable to prior art challenges. Its strategic position in the Australian patent landscape underscores its importance for stakeholders aiming to commercialize the associated drug or to carve out a competitive niche.


Key Takeaways

  • The patent's claims broadly cover a specific pharmaceutical composition and its therapeutic use, offering significant protection for the applicant.
  • The scope is tailored to include variations in formulation and application but may face challenges from existing prior arts.
  • A comprehensive landscape analysis suggests alignment with global patent families, reinforcing the development strategy.
  • Due diligence in FTO analysis is critical before commercialization to avoid infringing other patents.
  • The patent remains a valuable asset for licensing, partnership, and exclusivity in Australia.

FAQs

1. How does AU2015294912 compare to similar patents globally?
This patent generally aligns with international filings covering specific drug compositions and uses, often sharing common claims but tailored to Australian patent law.

2. What are the main risks to the patent’s enforceability?
Key risks include prior art invalidating inventive steps, narrow claim language, or challenges during patent opposition procedures.

3. How long does patent protection last for AU2015294912?
Standard Australian patents confer protection for 20 years from the filing date, subject to renewal payments.

4. Can this patent be challenged, and what are the grounds?
Yes, through opposition or validity proceedings based on lack of novelty, inventive step, or insufficient disclosure.

5. What steps should companies take to avoid infringing this patent?
Conduct detailed freedom-to-operate analyses, explore alternative formulations or methods, or negotiate licensing agreements.


References

  1. IP Australia, AU2015294912 Patent Specification.
  2. WIPO Worldwide Patent Database.
  3. Patent landscape reports concerning pharmaceutical patents in Australia.

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