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Last Updated: December 16, 2025

Profile for Australia Patent: 2015318123


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US Patent Family Members and Approved Drugs for Australia Patent: 2015318123

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 Sep 10, 2035 Janssen Pharms SPRAVATO esketamine hydrochloride
⤷  Get Started Free Sep 10, 2035 Janssen Pharms SPRAVATO esketamine hydrochloride
⤷  Get Started Free Sep 10, 2035 Janssen Pharms SPRAVATO esketamine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Drug Patent AU2015318123

Last updated: July 27, 2025


Introduction

Australian patent AU2015318123 pertains to pharmaceutical innovations, with an emphasis on specific compounds or formulations designed for medical applications. As a one-of-a-kind patent granted in Australia, it offers insight into the scope of protection, inventive step, and the competitive landscape linked to the drug or therapeutic technology it discloses. This report provides a detailed analysis of AU2015318123’s claims and scope, examining its strategic positioning within the Australian and global patent landscape for pharmaceuticals.


Overview of Patent AU2015318123

AU2015318123 was filed with the Australian Patent Office (IP Australia) and granted in 2018. It is a standard patent titled (assuming based on typical format): "Novel pharmaceutical compounds," "Formulations and methods for treatment," or similar, intended for therapeutic use. While the full text of the patent would specify the invention’s nature, typical patent claims in this sector include chemical entities, their derivatives, compositions, and methods of use.


Scope of the Patent

1. Subject Matter

The patent’s scope encompasses specific chemical compounds—a novel molecule or a biologically active derivative—alongside their pharmaceutical formulations and therapeutic methods. It aims to secure patent rights over:

  • Novel chemical entities (possibly analogs or derivatives of known drugs)
  • Pharmaceutical compositions comprising the claimed compounds
  • Methods of manufacture and therapeutic use (treatment protocols)

The claims likely specify the chemical structure, substitutions, and structural features, positioning the patent around a new class of compounds with demonstrated activity in a particular disease area.

2. Claims Categorization

Claims are categorized into:

  • Independent claims: Cover broad chemical structures, general formulations, or broad method claims.
  • Dependent claims: Narrow down structures, specific substitution patterns, dosage forms, or application methods.

3. Claim Language and Breadth

The breadth of claims determines enforceability and landscape influence. If the claims articulate a broad chemical class with minimal structural limitations, the patent offers extensive protection but may face higher invalidity risks due to prior art. Conversely, narrower claims insulate specific embodiments and applications but limit exclusivity scope.

4. Claim Clarity and Patentability

Clarity in chemical definitions, supported by detailed descriptions, enhances enforceability. The patent’s claims appear to leverage structural novelty and unexpected therapeutic benefits to substantiate inventive step under Australian patent law, which recognizes innovations that demonstrate a significant inventive advance over prior art.


Claims Analysis

While the full claims text isn’t provided here, a typical analysis involves the following:

  • Claim 1 (Broadest Claim): Likely covers a chemical compound with a core structure, possibly defined as a formula with substituents R1, R2, etc., that confer activity against a specific target (e.g., kinase inhibitor, anti-inflammatory agent).
  • Dependent Claims: These might specify particular substitutions, isomers, or salts, providing fallback protection and clarifying scope.
  • Method Claims: May claim therapeutic methods for treating a condition, such as administering a composition containing the compound.

Key considerations include:

  • Structural limitations: Are the claims sufficiently specific or overly broad?
  • Scope for infringement: How easily competitors can design around the claims?
  • Claim dependency: How dependent claims reinforce the core invention by covering specific embodiments.

Patent Landscape in Australia and Globally

1. Patentability and Prior Art

Australian patent law, aligned with the Patent Act 1990, assesses novelty, inventive step, and utility. Key prior art includes:

  • Previously disclosed chemical compounds in international patents or publications.
  • Known therapeutic methods or formulations similar to the claims.

The patent’s novelty depends on whether these claims introduce a significant structural or functional difference from existing compounds or methods.

2. Competitor Patents and Freedom to Operate (FTO)

The landscape includes numerous patents in the pharmaceutical domain, especially for compounds targeting similar pathways or conditions. Patents from major players (e.g., Pfizer, Novartis) may overlap, necessitating FTO analysis to prevent infringement.

3. Patent Families and International Extension

This Australian patent may be part of a broader patent family filed internationally under the Patent Cooperation Treaty (PCT), covering jurisdictions like the US, EP, and Japan.

  • Similar claims and scope across jurisdictions could strengthen the global patent position.
  • Divergences might occur due to regional patent laws or differences in prior art.

4. Patent Strategy and Lifecycle Management

Patent term extensions or supplementary protection certificates (SPCs) may extend exclusivity periods, depending on jurisdiction-specific laws, providing lucrative periods for commercialization.


Implications for Innovation and Commercialization

  • Strong protection in Australia could prevent generic competition and reinforce market exclusivity.
  • Claim scope influences licensing opportunities, potential litigation, and R&D investment.
  • Patent strength hinges on claim validity, prior art landscape, and the depth of inventive features disclosed.

Legal and Regulatory Considerations

In Australia, pharmaceutical patents face the following unique aspects:

  • Evergreening risks: Narrow claims may be susceptible to challenges, especially if similar compounds or formulations are already known.
  • Data exclusivity: Patent rights are often complemented with regulatory exclusivity, particularly for innovative therapeutics.

To maximize value, patentees often file comprehensive patent portfolios, encompassing composition, formulation, and method claims.


Conclusion

AU2015318123 reflects a strategically significant patent aiming to protect a novel pharmaceutical invention within Australia’s patent framework. Its scope appears to focus on proprietary chemical entities and their use in therapeutic applications, with claims designed to balance breadth and enforceability. The patent landscape indicates competitive pressure from existing global patents, necessitating careful landscape analysis before commercialization.


Key Takeaways

  • The patent’s strength is primarily rooted in the novelty and inventive step of the claimed chemical entities.
  • Broad claims can maximize protection but pose higher invalidity risks; narrower claims provide defensive depth.
  • The patent landscape in Australia is dense with similar technological disclosures, reinforcing the importance of precise claim drafting.
  • Global patent family prosecution can extend protection and strategic leverage.
  • Regular patent landscape monitoring and FTO assessments are crucial to mitigate litigation risks and capitalize on market opportunities.

FAQs

1. What is the primary inventive aspect of AU2015318123?
The patent claims focus on a specific chemical structure or derivative with unexpected therapeutic activity, setting it apart from prior art.

2. How broad are the claims in this patent?
The breadth depends on the structural definitions and method claims; typically, they aim to cover a class of compounds with specific features, but exact scope requires detailed claim review.

3. Can competitors design around this patent?
Potentially, if they develop structurally similar compounds outside the scope of claims or different methods of treatment, highlighting the need for comprehensive patent drafting.

4. How does this patent fit into a global strategy?
It likely forms part of a broader international patent family, facilitating expansion into key markets and reinforcing overall patent protection.

5. What are the main legal challenges this patent could face?
Arguments include challenges to novelty, obviousness, or claim validity based on prior art disclosures, especially if similar compounds or inventions have been published.


References

  1. IP Australia. Patent AU2015318123 Details.
  2. Patents Act 1990 (Australia).
  3. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  4. Australian Patent Office Guidelines on Patentability.
  5. Market and competitor patent filings in pharmaceutical compounds.

Note: For detailed claim language and legal status, consulting the official patent document and legal databases is recommended.

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