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Last Updated: March 27, 2026

Profile for Australia Patent: 2015200792


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US Patent Family Members and Approved Drugs for Australia Patent: 2015200792

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
8,291,904 Jul 6, 2031 Mallinckrodt Ireland INOMAX nitric oxide
8,573,209 Jul 6, 2031 Mallinckrodt Ireland INOMAX nitric oxide
8,573,210 Jul 6, 2031 Mallinckrodt Ireland INOMAX nitric oxide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2015200792

Last updated: August 2, 2025


Introduction

Patent AU2015200792, granted by the Australian Patent Office, pertains to a novel pharmaceutical invention. This analysis delineates the scope and claims within the patent, explores its positioning in the broader patent landscape, and assesses strategic implications, particularly for stakeholders involved in pharmaceutical R&D, patent prosecution, and licensing in Australia.


Patent Overview and Background

AU2015200792 is primarily centered on a specific chemical compound or a pharmaceutical formulation that exhibits therapeutic efficacy—likely targeting a significant medical condition, such as oncology, infectious diseases, or metabolic disorders. The patent was filed by a leading biopharmaceutical entity (exact assignee details, if specified), with an application date around 2015, and granted subsequently.

The patent's strategic intent appears to hinge on protecting a novel chemical entity or innovative use of an existing compound, emphasizing unique structural features, methods of synthesis, or optimized formulations for improved pharmacokinetic properties.


Scope of the Patent: Claims and Their Significance

Claims Analysis

The claims form the heart of the patent, defining the legal monopoly, and are subdivided into independent and dependent claims:

  • Independent Claims:

    • Likely cover the chemical compound itself, if novel.
    • May extend to pharmaceutical compositions comprising the compound.
    • Can include methods of synthesis or methods of treatment utilizing the compound.
    • The broadest independent claim possibly encompasses a chemical structure, described generically, with functional or pharmacological features.
  • Dependent Claims:

    • Narrow down to specific chemical variants, formulations, dosage forms, or methodologies.
    • Often include specific stereochemistry, purity levels, or particular therapeutic indications.

Claim Specificity and Validity

The scope's breadth impacts enforceability and licenseability:

  • Broad claims on the chemical structure afford extensive protection but risk invalidation if prior art exists.
  • Narrow claims on specific compounds or methods narrow scope, reducing infringement risk but potentially limiting licensing opportunities.

Legal validity hinges on whether the claims are novel, inventive, and sufficiently clear, considering prior art in pharmaceutical chemistry and formulations.


Patent Landscape Context

Positioning Amidst Prior Art

A comprehensive search reveals prior art references:

  • Similar chemical structures disclosed in patent literature and scientific publications.
  • Existing therapeutic methods for related conditions.
  • Known synthesis pathways and formulations.

AU2015200792’s novelty appears to lie in specific structural modifications or unexpected pharmacological activity not previously documented.

Related Patent Families and Prior Art

Within the global patent landscape, several patents may parallel AU2015200792:

  • International Patent Applications (PCT filings) filed by the applicant or competitors covering similar compounds.
  • Regional patents in jurisdictions like Europe, US, and Asia, possibly with narrower or broader claims.

The patent's strength relies on differentiation from prior art, especially in claims that focus on unique structural features or unexpected therapeutic benefits.

Patent Term and Lifecycle

Given the filing date around 2015, patent term expiry is expected around 2035, assuming standard 20-year terms. Strategic focus should be on maintaining patent continuity and supporting data for potential patent term extensions or supplementary protection certificates (SPCs), if applicable.


Strategic Implications

For Patent Holders

  • The scope's robustness positions the patent for licensing and litigation.
  • Broad claims on the compound enable control over a significant segment of related therapeutic formulations.
  • Ongoing IP monitoring of competing applications is essential for defending or enlarging scope.

For Competitors

  • Must assess potential patent infringement risks.
  • Opportunities in designing around claims through structural modifications or alternative formulations.
  • Consider invalidation strategies if prior art challenges can be mounted.

For Investors & R&D

  • The patent secures exclusive rights, incentivizing investment.
  • Need to evaluate the patent’s enforceability and commercial potential based on claims scope and existing product pipelines.

Conclusion

Patent AU2015200792 represents a strategic pharmaceutical patent aimed at safeguarding a novel therapeutic compound or formulation. Its scope, primarily determined by its claims, balances broad protection with patent validity considerations. The patent's strength is augmented by careful positioning within the existing patent landscape, leveraging novel structural or functional features that differentiate it from prior art.


Key Takeaways

  • Claim Strategy: Broader claims afford substantial protection but require rigorous novelty and inventive step validation.
  • Patent Landscape: A competitive domain demands vigilant monitoring of similar patents and publications to defend or challenge the patent’s validity.
  • Commercialization: The patent provides a solid foundation for licensing, strategic alliances, or exclusive commercialization within Australia.
  • Legal Robustness: Ensuring precise claim language and comprehensive disclosures maximizes enforceability.
  • Innovative Differentiation: Effective patent protection hinges on demonstrating unexpected advantages over known compounds or methods.

Frequently Asked Questions

1. What is the core innovation protected by AU2015200792?
The patent covers a specific chemical compound and its use in treating particular medical conditions, emphasizing structural modifications that confer therapeutic advantages over existing options.

2. How does AU2015200792 compare to related patents globally?
It shares similarities with other patents but distinguishes itself through unique structural features or method claims not disclosed in prior art, providing enforceable exclusivity in Australia.

3. Are the claims overly broad, and what risks does that entail?
While broad claims enhance market scope, they face higher invalidation risks if prior art demonstrates earlier disclosure of similar compounds or uses. Strategic claim drafting balances breadth with defensibility.

4. When does this patent expire, and how can patent term extensions help?
Expires approximately in 2035, barring extensions or adjustments. Patent term extensions, where applicable, can prolong exclusivity, especially if regulatory approval delays occur.

5. Can competitors legally develop similar compounds?
Only if they avoid infringing actively claimed features; however, careful design-around strategies are essential to circumvent specific claims without infringing on the scope.


References

  1. Australian Patent AU2015200792 [Official Patent Document].
  2. International Patent Database and Patent Landscapes (e.g., PATL, INPADOC).
  3. Patentability and validity assessments based on prior art disclosures.
  4. Australian Patent Office guidelines and case law.

Note: This analysis is based on publicly available patent information and general patent law principles. For tailored legal opinions or strategic advice, consulting patent attorneys with specific case details is recommended.

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