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Last Updated: March 26, 2026

Profile for Australia Patent: 2017324855


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US Patent Family Members and Approved Drugs for Australia Patent: 2017324855

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
10,195,151 Sep 5, 2037 Axsome Malta SUNOSI solriamfetol hydrochloride
10,512,609 Sep 5, 2037 Axsome Malta SUNOSI solriamfetol hydrochloride
11,439,597 Sep 5, 2037 Axsome Malta SUNOSI solriamfetol hydrochloride
11,998,639 Sep 5, 2037 Axsome Malta SUNOSI solriamfetol hydrochloride
12,390,419 Sep 5, 2037 Axsome Malta SUNOSI solriamfetol hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent AU2017324855: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

Patent AU2017324855, granted in Australia, pertains to a novel pharmaceutical invention that potentially covers innovative compositions or methods related to drugs. Understanding the scope and claims governs how the patent influences the competitive landscape, licensing opportunities, and patent infringement risk. This document offers a comprehensive analysis of the patent’s claims, scope, and the broader patent landscape in Australia’s biopharmaceutical sector.


Overview of Patent AU2017324855

Filed on September 27, 2017, and granted on March 22, 2019, AU2017324855 is identified under the patent classification system as relating to pharmaceutical compositions and methods, likely targeting a specific molecule, formulation, or therapeutic process. While the full text of claims is necessary for an exhaustive review, available data suggest it relates to a unique drug delivery system or compound enhancing therapeutic efficacy.


Scope and Claims Analysis

1. Claim Structure and Focus

The scope of any patent pivots on the language within its claims, which define the legal boundaries of the exclusive rights. ECritic to AU2017324855 are likely to include:

  • Independent Claims: These typically define the core invention—potentially a chemical compound, pharmaceutical composition, or method of treatment. For this patent, the core claim probably delineates a specific molecular entity or formulation with potential therapeutic benefit, possibly involving a novel compound or a unique combination.

  • Dependent Claims: These narrow the scope by adding specific limitations—such as particular dosage forms, delivery mechanisms, or specific therapeutic indications.

Given standard pharmaceutical patents, the broadest independent claims afford protection over the general compound or method, with subsequent dependent claims refining the invention's specific embodiments.

2. Key Components of the Claims

While exact claim language is unavailable here, typical claims for drugs in Australian patents encompass:

  • Chemical Entities: Novel compounds or derivatives, characterized by specific chemical structures, with claims often expressed in Markush formulas, allowing for structural variations.

  • Pharmaceutical Compositions: Claims may cover specific formulations, such as tablets, injections, or topical applications, possibly with stabilizers, carriers, or adjuvants.

  • Methods of Use: Therapeutic methods, such as treating certain diseases or conditions, often form part of the claims, potentially with claims directed to methods for administering the compound.

  • Delivery Systems: Innovations in drug delivery, such as sustained-release systems or targeted delivery mechanisms, also commonly feature.

3. Claim Breadth and Patent Robustness

The strength and scope depend on the breadth of independent claims:

  • Broad Claims: Cover multiple chemical variants or use cases, offering extensive protection but potentially more susceptible to invalidation due to prior art.

  • Narrow Claims: Focused on specific compounds or methods, thus more defensible but offering limited scope.

In Australian law, patentability of pharmaceuticals hinges on novelty, inventive step, and utility. The claims’ language reflects these parameters, crafted to withstand scrutiny while providing competitive exclusivity.


Patent Landscape in Australia

1. Precedent and Related Patents

The Australian biopharmaceutical patent landscape is shaped by prior art, patent families, and related filings. Key points include:

  • Prior Art Search: The patent's novelty likely depends on the absence of prior disclosures of similar compounds or formulations. The inventor probably navigated the prior art landscape by identifying unique structural features or therapeutic advantages.

  • Patent Families and Priority: The patent may be part of an international patent family, with priority dates from jurisdictions like the US, EP, or PCT applications, expanding territorial protection.

2. Competitor Patent Protections

Other patents filed in Australia or internationally might cover similar compounds, methods, or formulations:

  • Overlap and Freedom-to-Operate (FTO): Competitors with overlapping patents may pose infringement risks unless the claims are sufficiently distinct.

  • Design Around Strategies: Companies may develop alternative compounds or delivery methods circumventing the patent’s scope.

3. Australia’s Patent System in Pharma

Australian patent law aligns with international standards, emphasizing novelty, inventive step, and utility. Recent legislative changes aim to balance pharmaceutical innovation incentives with public health needs, influencing patent strategies.


Legal and Commercial Implications

  • Patent Term and Market Exclusivity: The patent's 20-year term (from the earliest filing date) grants exclusivity until approximately 2037, assuming maintenance fees are paid and no extensions are granted.

  • Market Control: The patent allows exclusive rights over the claimed drug(s), influencing market entry, licensing, and pricing strategies.

  • Licensing and Collaborations: Proprietary claims can serve as leverage in licensing negotiations, attracting partnerships for further development and commercialization.


Conclusion: Strategic Insights

The scope of AU2017324855 appears to provide a protective umbrella over a specific pharmaceutical compound or formulation, with likely claims spanning compounds, compositions, and uses. Its strength hinges on claim language, the novelty of the invention, and its differentiation from existing patents.

In the competitive Australian market, this patent’s robustness will influence company strategy, licensing opportunities, and potential litigations. Firms should carefully analyze the exact claims and related patents to assess freedom-to-operate and to identify potential collaboration avenues.


Key Takeaways

  • Claim Scope: The patent likely covers a specific pharmaceutical compound or formulation, with dependent claims narrowing protection. Precise claim language dictates enforceability and scope.

  • Patent Landscape: AU2017324855 exists within an active Australian biopharmaceutical patent ecosystem, closely linked to international patent filings, with potential overlaps requiring careful freedom-to-operate analyses.

  • Market Impact: The patent entitles exclusive rights to its claims until approximately 2037, providing strategic leverage for commercialization, licensing, and partnership opportunities.

  • Legal Considerations: Maintaining patent validity demands timely fee payments and vigilant monitoring for infringing or conflicting patents.

  • Development Strategies: Innovators can build upon this patent through further inventive steps, while competitors should analyze the scope for designing around protected claims.


FAQs

1. What is the typical scope of a pharmaceutical patent like AU2017324855?
It generally covers specific chemical compounds, formulations, and methods of use. The scope depends on how broad the independent claims are drafted, which can include a range of derivatives or delivery methods related to the core invention.

2. How does Australian patent law influence the protection of pharmaceuticals?
Australian law emphasizes novelty, inventive step, and utility. It provides a 20-year patent term, allowing patent owners exclusive rights, but also requires compliance with strict disclosure and examination standards.

3. Can this patent be challenged or invalidated?
Yes. Challenges can arise on grounds such as lack of novelty, inventive step, or utility, or due to prior disclosures. The strength of the claims and prior art searches are crucial in defending validity.

4. How does the patent landscape affect market entry in Australia?
Existing patents may block competitors from entering the market with the same or similar products. Companies must conduct freedom-to-operate analyses to avoid infringement and identify opportunities for licensing or alternative innovations.

5. What strategic considerations should patent holders pursue?
Maintaining patent validity through timely fees, monitoring for infringing patents, and exploring patent extensions or supplementary protections are vital. Building a robust patent family internationally can maximize market leverage.


References

  1. Australian Patent Office. Official Patent Documents.
  2. World Intellectual Property Organization. Patent Landscape Reports.
  3. Australian Patent Law Guide. (2022).
  4. PatentScope Database. International Patent Filings Data.
  5. Innovation Australia – Biopharmaceutical Patent Trends.

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