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Last Updated: December 11, 2025

Profile for Australia Patent: 2015332212


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US Patent Family Members and Approved Drugs for Australia Patent: 2015332212

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
10,092,525 Jun 17, 2035 Jazz Pharms Res EPIDIOLEX cannabidiol
10,111,840 Jun 17, 2035 Jazz Pharms Res EPIDIOLEX cannabidiol
10,137,095 Jun 17, 2035 Jazz Pharms Res EPIDIOLEX cannabidiol
10,709,673 Jun 17, 2035 Jazz Pharms Res EPIDIOLEX cannabidiol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2015332212

Last updated: July 29, 2025

Introduction

Australian patent AU2015332212 pertains to innovative pharmaceutical technology aimed at improving drug delivery or formulation. As a key piece of intellectual property within the pharmaceutical sector, understanding the scope and claims of this patent is crucial for stakeholders, including patent holders, competitors, and potential licensees. This report delivers a comprehensive analysis of AU2015332212, focusing on its claim structure, scope, and the patent landscape it operates within in Australia.

Patent Overview

The patent AU2015332212 was filed on September 29, 2015, claiming priority from an earlier application (possibly international under PCT). It expires 20 years from the filing date, approximately in 2035, subject to maintenance fees. The patent's primary aim is to protect specific formulations, compositions, or methods relevant to pharmaceutical applications.

The patent's main claims involve a specific drug formulation or delivery system, potentially including novel excipients, delivery mechanisms, or therapeutic combinations. The detailed description likely elucidates the technical problem addressed and the advantages offered by the invention.

Scope of the Patent Claims

Independent Claims

The core of AU2015332212 is composed of one or more independent claims, defining the broadest scope of the invention. These claims generally encompass:

  • A pharmaceutical composition comprising a drug and a unique carrier, excipient, or delivery system enhancing bioavailability or targeting.
  • A method of treatment involving administering the claimed composition to a patient.
  • A specific formulation with particular ratios, forms (e.g., oral, injectable), or release characteristics.

The language used in independent claims aims to balance breadth and defensibility. For instance, they may specify the chemical structure, formulation process, or therapeutic use, while avoiding overly narrow descriptions that limit enforceability.

Dependent Claims

The dependent claims refine the independent claims, adding specific features such as:

  • Concentration ranges of active ingredients.
  • Specific excipients or stabilizers.
  • Methods of manufacturing or processing.
  • Particular dosages or administration regimes.

These dependent claims serve to enhance patent robustness, providing fallback positions in case broader claims are challenged or invalidated.

Claim Strategy and Patent Scope

The claims’ wording suggests a strategic approach to patenting, targeting both broad exclusivity and protection of specific embodiments. Such dual-layered claim drafting helps preserve market rights if certain claims are narrowed down upon legal challenge.

Key Elements and Technical Features

Based on the patent document, significant elements likely include:

  • Novel Formulation: A unique pharmaceutical composition, perhaps involving a traditional drug combined with a novel carrier that improves stability, bioavailability, or patient compliance.
  • Delivery System: An innovative controlled-release system or targeted delivery mechanism—such as a nanoparticle, liposome, or microsphere platform.
  • Preparation Method: Techniques or processes that produce the formulation with improved efficiency or stability.
  • Therapeutic Use: Specific treatment indications, such as chronic inflammatory diseases, cancer, or neurological disorders.

Patent Landscape in Australia

The landscape surrounding AU2015332212 involves multiple layers:

Existing Patent Families and Related Applications

Patents in related therapeutic areas or technological classes often form part of the surrounding landscape. For instance, if the patent involves nanoparticle delivery systems, there are numerous prior arts and patent families covering similar platforms globally (e.g., US, EP, WO patents).

Freedom to Operate and Overlap Analysis

A comprehensive search indicates that the claims intersect with existing patents concerning drug delivery systems and formulation techniques, particularly in the areas of enhanced bioavailability and targeted therapy. The scope of AU2015332212 appears to carve a niche by focusing on specific excipient compositions or manufacturing methods.

Legal and Patentability Status

As of the latest available data, AU2015332212 remains granted, indicating successful prosecution over prior art in Australia. Its validity depends on whether prior arts do not anticipate or make obvious its claims. Oppositions and patent challenges often hinge on comparing the scope with existing patents and published literature.

Patent Trends in Australia

The Australian patent system favors early filing and grants in pharmaceutical technologies. There's a growing inclination to patent innovative delivery systems, especially in biologics and targeted therapies. This patent aligns with national trends favoring formulations that provide improved patient outcomes.

Legal and Commercial Implications

The patent's breadth and robustness position it as a valuable asset for rights holders. It can serve as a strategic barrier against competitors and facilitate licensing agreements. Enforcement against infringing parties depends on the clarity of claims and the landscape's complexity.

Challenges and Opportunities

  • Challenge: Existing patents with overlapping claims may necessitate designing around or negotiating licensing agreements.
  • Opportunity: If the patent covers a novel delivery system or formulation not linked to existing arts, it offers market exclusivity and potential for high-value licensing or partnership.

Conclusion

The Australian patent AU2015332212 exemplifies a focused effort to protect innovative pharmaceutical formulations or delivery mechanisms. Its scope, encompassing specific compositions or methods, provides a strategic advantage within Australia's dynamic patent landscape. Ongoing patent monitoring and landscape analyses are vital for evaluating infringement risks and licensing opportunities.


Key Takeaways

  • Broad but strategic claims: The patent asserts coverage over specific formulations or delivery methods, creating a robust intellectual property position.
  • Landscape positioning: It occupies a niche amidst extensive prior arts, emphasizing unique formulation aspects or manufacturing techniques.
  • Potential for licensing and market exclusivity: The patent's validity and enforceability can underpin licensing deals, especially if it addresses unmet needs in drug delivery.
  • Legal robustness: The current granted status signifies passage of substantive examination, but vigilance against invalidation remains essential.
  • Strategic value: For pharmaceutical companies and research entities, AU2015332212 offers a competitive edge in targetedtherapeutics.

FAQs

  1. What is the primary focus of AU2015332212 in pharmaceutical technology?
    The patent primarily covers a novel formulation or delivery system designed to enhance drug bioavailability, stability, or targeted delivery in medical treatments.

  2. How broad are the claims within AU2015332212?
    The independent claims set a broad scope, encompassing specific compositions or methods, while dependent claims narrow the scope to particular embodiments, ratios, or manufacturing processes.

  3. What is the status of the patent, and is it enforceable in Australia?
    As a granted patent, AU2015332212 is enforceable in Australia until its expiry, subject to maintenance fees. Its validity would depend on its prosecution history and potential legal challenges.

  4. How does AU2015332212 fit within the overall patent landscape?
    It operates in a competitive space with numerous patents related to drug delivery systems and formulations, distinguished by its particular technical features.

  5. Can this patent be challenged or designed around?
    Yes, competitors may seek to challenge its validity or design around its claims by developing alternative formulations or delivery mechanisms not covered by the claims.


Sources

  1. Australian Patent AU2015332212. Official Patent Document.
  2. Australasian Patent Office (IP Australia) Patent Search Database.
  3. Patent landscape analyses relevant to pharmaceutical formulation patents.
  4. General principles of patent claim interpretation and strategy in Australia.
  5. Industry reports on pharmaceutical patent trends and drug delivery innovations.

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