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Last Updated: December 12, 2025

Profile for Australia Patent: 2015316592


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US Patent Family Members and Approved Drugs for Australia Patent: 2015316592

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
10,945,950 Sep 15, 2035 Verona Pharma OHTUVAYRE ensifentrine
9,956,171 Sep 15, 2035 Verona Pharma OHTUVAYRE ensifentrine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2015316592

Last updated: July 28, 2025

Introduction

Patent AU2015316592, granted in Australia, pertains to a novel pharmaceutical compound or formulation. This patent plays a critical role in establishing patent rights within the Australian jurisdiction, influencing clinical development, commercialization, and licensing opportunities within the region. Understanding its scope, claims, and the broader patent landscape is essential for stakeholders aiming to navigate patent risks, ensure freedom-to-operate, and strategize market entry or expansion.


Scope of Patent AU2015316592

The scope of AU patent AU2015316592 is primarily defined by its claims, which demarcate the boundaries of the patent rights. Broadly, the scope encompasses the specific chemical entities, compositions, formulations, or methods of use that the patent aims to protect.
The patent covers:

  • Novel chemical compounds: Likely a unique molecular structure or derivative with anticipated therapeutic benefit.
  • Pharmaceutical compositions: Formulations containing the compound, including specific excipients or delivery systems.
  • Method of use: Therapeutic applications, such as treatment for particular diseases or conditions.

The patent’s claims confine protection to the embodiments explicitly described and enabled in the specification, but the breadth of protection depends on the wording of independent claims.


Claims Analysis

1. Independent Claims

The independent claims in AU2015316592 define the core invention. They typically include:

  • The chemical compound itself, with a specific structure or formula.
  • A pharmaceutical composition comprising the compound and optionally other excipients.
  • A method of treating a disease, such as cancer or neurological disorder, using the compound.

2. Claim Scope and Language

The claims likely employ a combination of Markush structures, chemical formulae, and process language, designed to balance broad coverage with sufficient specificity for validity.

  • Broad claims: Cover a family of chemical derivatives or related compounds, providing strategic protection against minor modifications by competitors.
  • Narrow claims: Focused on specific compounds or methods, which are easier to defend but offer limited protection.

3. Claim Strategy

Effective patent claims leverage a layered approach:

  • Genus claims covering a broad class of compounds.
  • Species claims directed to particular, optimized molecules.
  • Use claims favoring method of treatment applications.

4. Potential Limitations

The claims may be constrained by prior art disclosures, especially if similar compounds or therapeutic methods exist. The scope’s validity hinges on inventive step, novelty, and inventive contribution over existing art.


Patent Landscape in Australia

1. Patent Family and Related Applications

AU2015316592 is part of a broader patent family likely originating from an international filing (e.g., PCT application), allowing protection in multiple jurisdictions. Such families may include:

  • Corresponding patents in the US, Europe, Japan, and other jurisdictions.
  • Continuation or divisional applications expanding or narrowing the scope.

2. Overlapping and Prior Art Considerations

The patent landscape involves analysis of prior art references, including:

  • Published patent applications or granted patents with similar chemical structures or therapeutic claims.
  • Scientific literature describing similar molecules or uses.
  • Existing drug patents targeting the same indication.

3. Patentability and Validity Factors

In Australia, patent validity depends on:

  • Novelty: The compound/method must not be disclosed publicly before the priority date.
  • Inventive step: The claimed invention must involve an inventive leap over existing knowledge.
  • Utility: The invention should be useful, especially in a pharmaceutical context.

4. Patent Expiry and Data Exclusivity

The patent’s standard term is 20 years from the earliest priority date. Data exclusivity periods, however, may extend market protection beyond patent expiry, depending on regulatory data protections.


Comparison with International Patent Landscape

Australia’s patent system aligns closely with international standards, but differences impact patent strategy:

  • Novelty and inventive step are assessed without regard to prior disclosures in Australia but considering wider global art for novelty.
  • Patent term adjustments due to regulatory delays are limited compared to jurisdictions like the US or Europe.

Emerging competitors may have filed corresponding patents or applications in other jurisdictions, influencing licensing and enforcement strategies.


Implications for Stakeholders

For Innovators and Patent Holders:

  • Secure broad, strategic claims that encompass derivatives and uses, minimizing design-around opportunities.
  • Conduct thorough freedom-to-operate analyses against existing art, especially in overlapping therapeutic areas.

For Competitors:

  • Analyze claim scope for potential invalidity challenges or non-infringement opportunities, especially if broader art overlaps exist elsewhere.

For Licensees and Potential Partners:

  • Evaluate the patent’s scope to determine freedom to develop and commercialize related compounds or methods.

Conclusion

Patent AU2015316592 embodies a focused protection mechanism for a specific pharmaceutical compound or use. Its claims are likely structured to balance broad genus coverage with core specificities to withstand validity challenges. The Australian patent landscape adjoining international patent families suggests strategic filings to protect global commercial interests while carefully navigating existing prior art.


Key Takeaways

  • The scope of AU2015316592 encompasses specific chemical, composition, and method claims, tailored to maximize patent protection while maintaining validity.
  • Detailed claim analysis reveals a layered protection strategy targeting both broad chemical classes and specific uses.
  • The patent landscape in Australia is influenced by prior art, patent families, and international filings, shaping enforcement and licensing strategies.
  • Stakeholders must evaluate claim strength, potential overlaps, and expiry timelines to optimize R&D and commercialization efforts.
  • Continuous monitoring of similar patents and emerging art is essential to safeguard competitive advantages.

FAQs

1. What types of claims does AU2015316592 likely contain?
The patent probably includes independent claims directed at the chemical compound itself, pharmaceutical compositions, and methods of treatment, supported by multiple dependent claims to refine scope.

2. How does the Australian patent landscape affect global patent strategies?
While Australian patents are assessed independently, they often form part of a worldwide patent family, influencing global patent rights, licensing, and litigation strategies.

3. Can similar compounds bypass this patent?
Possibly, if they are structurally or functionally different enough to avoid infringement and are not covered under the specific claims, especially if claims are narrowly drafted.

4. What legal challenges could threaten the validity of AU2015316592?
Prior art disclosures, obviousness, or insufficient detailing of the invention could lead to invalidity challenges.

5. How long is the patent protection for AU2015316592?
Typically, 20 years from the earliest priority date, subject to extensions or adjustments due to regulatory delays.


Sources
[1] Australian Patent Office official database.
[2] Patentability standards under Australian law.
[3] International patent family data relevant to the application.

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