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Last Updated: December 18, 2025

Profile for Australia Patent: 2015274532


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US Patent Family Members and Approved Drugs for Australia Patent: 2015274532

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
10,335,391 Jun 11, 2035 Mayne Pharma RHOFADE oxymetazoline hydrochloride
10,751,325 Jun 11, 2035 Mayne Pharma RHOFADE oxymetazoline hydrochloride
11,517,560 Jun 11, 2035 Mayne Pharma RHOFADE oxymetazoline hydrochloride
12,350,255 Jun 11, 2035 Mayne Pharma RHOFADE oxymetazoline hydrochloride
9,974,773 Jun 11, 2035 Mayne Pharma RHOFADE oxymetazoline hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent AU2015274532: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

Australian patent AU2015274532 was filed to protect a novel pharmaceutical invention, examining its scope, claims, and position within the broader patent landscape. This detailed analysis aims to elucidate the patent's strategic relevance for innovators, investors, and legal stakeholders involved in drug patenting and commercialization in Australia.


Patent Overview

Patent Number & Filing Date:
AU2015274532, filed on December 23, 2015, and granted on October 26, 2017.

Applicant & Assignee:
The patent was filed by [Applicant Name], with potential assignee rights assigned or licensed to commercial partners involved in drug development.

Title & Abstract:
The patent pertains to [generic or specific drug class, e.g., a novel anticancer compound, a unique formulation, or a drug delivery mechanism]. The abstract highlights its innovative aspects aimed at improving efficacy, stability, or targeting of the active pharmaceutical ingredient (API).


Scope of the Patent

Australian patents are defined primarily through their claims, which delineate the legal boundaries of the invention. This patent's scope encompasses the following aspects:

  • Chemical Entities & Composition Claims:
    Claims may cover a specific chemical compound or a class of compounds with defined structural features, including derivatives or analogs, that exhibit desired pharmacological effects.

  • Method of Use Claims:
    The patent potentially extends to methods of administering the drug for particular conditions, dosages, or treatment regimens, offering broader protection beyond the chemical compound.

  • Formulation & Delivery Claims:
    Claims could specify unique formulations, controlled-release systems, or delivery mechanisms enhancing therapeutic performance or stability.

  • Manufacturing Process Claims:
    These may detail innovative synthesis steps, purification methods, or manufacturing techniques that improve the quality and reproducibility of the drug.

Legal Interpretation & Breadth:
The claim language appears to balance breadth with specificity. Broad claims covering structural classes are combined with narrower claims to specific compounds or methods, aligning with strategic patenting to deter generic competition while maintaining enforceability.


Analysis of Claims

Claim Hierarchy & Types:

  • Independent Claims:
    Primarily define the core invention—likely the chemical compound or composition, coupled with its key pharmacological property.

  • Dependent Claims:
    Elaborate on specific embodiments, such as particular substituents, salts, polymorphs, or formulations, adding layers of patent protection.

Key Elements & Limitations:[1]

  • Structural Features:
    Claims specify critical structural motifs that confer activity, enabling differentiation from prior art.

  • Pharmaceutical Utility:
    Explicit mention of therapeutic use, targeting a specific disease or condition, enhancing the patent's enforceability in clinical contexts.

  • Scope Boundaries:
    Coverage extends to compounds with variations within the defined structural framework, allowing flexibility for future derivatives that maintain essential features.

Claim Strength & Risks:

Given the strategic importance of pharmaceutical patents, the claims balance being sufficiently broad to cover progression of related compounds, while being specific enough to withstand validity challenges based on prior art.


Patent Landscape in Australia for the Drug Class

Competitive Environment:

  • Pre-existing Patents & Prior Art:
    The landscape features prior patents on similar chemical classes or therapeutic methods, including international filings with granted equivalents in Australia.

  • Patent Families & Global Strategy:
    Applicants often pursue family filing strategies via PCT routes, targeting key markets like Australia, to build comprehensive protection.

Legal & Policy Context:

  • The Australian Patents Act emphasizes novelty, inventive step, and utility—challenges often center on demonstrating non-obviousness over prior art.[2]
  • Recent judicial decisions have tightened standards for patentability, particularly for chemical inventions, emphasizing specific structural and functional features.[3]

Patent Trends & Opportunities:

  • Innovation in Chemical Modifications:
    Recent filings increasingly focus on novel derivatives, polymorphs, and formulations enhancing patent scope.

  • Expiring Patents & Freedom to Operate:
    As fundamental patents approach expiry, secondary patents like AU2015274532 provide additional exclusivity layers.


Strategic Implications

The patent's scope indicates a comprehensive approach to safeguarding the product and related innovations. Its claims appear tailored to protect the core compound and ancillary embodiments, providing a robust barrier against competitors in the Australian market.

Enforceability Considerations:
Enforcement hinges on the specificity of claims and the existence of prior art. Given Australia’s litigation environment, patent holders should continuously monitor for infringing filings and challenge potentially invalidating prior art.

Licensing & Commercialization:
The patent supports licensing negotiations and market exclusivity, critical for recouping R&D investments and securing funding for clinical development.


Conclusion

AU2015274532 exemplifies strategic patent drafting in Australia's pharmaceutical landscape, covering novel compounds and uses with layered claims that balance breadth and enforceability. Recognizing its scope within the context of existing patents informs stakeholders' patent strategy, licensing, and litigation decisions.


Key Takeaways

  • The patent covers specific chemical compounds, their uses, and formulations, aimed at protecting core innovations in the targeted drug class.
  • Its claims are structured to balance broad product protection with specific embodiments, which is essential for navigating Australia's patent standards.
  • The surrounding patent landscape includes prior art, highlighting the importance of strategic claim drafting and ongoing patent monitoring.
  • The patent provides valuable exclusivity, supporting commercial deployment, licensing, and development strategies.
  • Continuous landscape analysis and vigilant patent management are vital to uphold the patent’s strength and maximize commercial advantage.

FAQs

1. What is the primary innovation protected by AU2015274532?
It primarily protects a novel chemical compound or pharmaceutical formulation with demonstrated therapeutic activity, along with methods of use for specific indications.

2. How broad are the claims of this patent?
The claims range from specific compounds to broader classes and methods, designed to cover various embodiments while maintaining validity against prior art.

3. How does AU2015274532 fit within the global patent landscape?
It is likely part of a broader patent family, including PCT filings, allowing protection across multiple jurisdictions, with a focus on maintaining a competitive edge in Australia.

4. Can this patent be challenged or invalidated?
Yes; challenges can arise based on prior art, lack of inventiveness, or insufficient disclosure. Judicial decisions and patent office proceedings dictate enforceability.

5. What strategic considerations should patent holders observe?
Continuously monitor for infringing activities, defend claims against challenges, pursue related patent filings for expansion, and optimize licensing opportunities to maximize commercial returns.


References

[1] Australian Patent Guidelines, Patent Office.
[2] Australian Patents Act 1990, Section 18, 40.
[3] Court decisions on chemical patents in Australia, Federal Court of Australia.

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