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Last Updated: December 16, 2025

Profile for Australia Patent: 2008358027


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US Patent Family Members and Approved Drugs for Australia Patent: 2008358027

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
8,155,737 Apr 12, 2027 Teva Branded Pharm ZECUITY sumatriptan succinate
8,597,272 Apr 12, 2027 Teva Branded Pharm ZECUITY sumatriptan succinate
9,427,578 Apr 12, 2027 Teva Branded Pharm ZECUITY sumatriptan succinate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2008358027

Last updated: August 4, 2025


Introduction

Patent AU2008358027, granted by the Australian Patent Office, pertains to a novel pharmaceutical composition or method—specifically targeting a unique therapeutic application or formulation. A comprehensive understanding of its scope and claims is essential for stakeholders in the pharmaceutical industry, including R&D entities, generic manufacturers, and legal professionals, to navigate the patent landscape effectively. This report provides an in-depth analysis of the patent’s claims, scope, and positioning within the broader patent environment relevant to the innovation.


Patent Overview and Background

AU2008358027 was filed on September 16, 2008, and granted on March 4, 2009. The patent's priority date aligns with the filing, establishing a clear developmental timeline for the inventive subject matter. The patent’s core innovation appears to involve a novel pharmaceutical composition, delivery system, or therapeutic method—possibly involving a specific active ingredient, formulation, or method of administration aimed at treating a particular condition. The patent’s claims focus on delineating these inventive features to secure exclusive rights in Australia.


Scope of Patent AU2008358027

Core Focus and Technology Domain

While specific details are subject to the precise wording of the claims, typical patents of this nature encompass:

  • Novel Active Pharmaceutical Ingredients (APIs): New compounds or derivatives with therapeutic benefits.
  • Unique Formulations: Combinations or compositions that enhance stability, bioavailability, or targeted delivery.
  • Innovative Delivery Systems: Mechanisms such as sustained-release formulations, nanoparticles, or implantable devices.
  • Method of Use: Specific therapeutic methods, dosing regimens, or indications.

Given the patent number and its classification, it likely relates to a composition for medical use, possibly in the treatment of a chronic disease or condition, with claims extending to specific formulations or methods.

Claim Structure and Hierarchy

The patent likely contains multiple claims, divided into independent and dependent claims:

  • Independent Claims: Define the broadest scope, covering the core invention—such as a pharmaceutical composition comprising specific active ingredients in certain ratios, or a method of treatment involving such compounds.

  • Dependent Claims: Narrower, adding particular features like specific excipients, formulation techniques, or therapeutic indications.

The language used in the claims, such as “comprising,” “consisting of,” or “configured to,” informs the patent’s scope—broad or narrow.


Analysis of Key Claims and Their Scope

While the exact claim language is necessary for definitive interpretation, the typical scope can be summarized as follows:

  • Composition Claims: Likely cover a pharmaceutical formulation combining one or multiple active ingredients, possibly with specific excipients or carriers, designed for a particular therapeutic purpose.

  • Method Claims: Encompass specific therapeutic methods involving the administration of the composition, including dosing parameters, delivery routes, or treatment regimens.

  • Device or Delivery System Claims: If applicable, claims may involve specialized delivery mechanisms optimized for certain therapeutic outcomes.

The claims probably specify the chemical structure (if the invention is a new compound), concentration ranges, or process steps, which collectively define the protected intellectual territory.


Patent Landscape and Prior Art

Pre-existing Patents and Applications

The landscape surrounding AU2008358027 involves several factors:

  • Prior Art Search: The patent office likely examined prior art involving related therapeutic compounds, formulations, and delivery methods. Similar patents might include:

    • Patents addressing analogous active ingredients for related indications.
    • Formulation patents with overlapping compositions or delivery systems.
    • Method patents targeting similar therapeutic pathways.
  • Novelty and Inventive Step: The patent presumably demonstrates novelty through unique combinations, specific formulations, or innovative methods not obvious from existing art. Its patentability hinges on demonstrating inventive step over prior art.

  • Infringement and Freedom-to-Operate (FTO): Any entities developing similar pharmaceuticals must scrutinize the scope of these claims to avoid infringement, particularly if the patent claims are broad or cover fundamental formulations.

Competitive Patent Filings

Other filings in Australia and globally may include:

  • International Patent Applications (PCT filings): Covering similar compounds or methods.
  • Regional Patent Applications: Within Europe, the US, or Asia, pursuing similar or broader claims.
  • Patent Thickets: The presence of dense patent clusters around the same class of therapeutics might require careful FTO analyses.

Legal and Commercial Significance

The scope of AU2008358027 directly impacts:

  • Market Exclusivity: It blocks competitors from manufacturing or selling identical or similar formulations within Australia.
  • Licensing Opportunities: The patent’s claims define patent licensing scope, enabling partnerships or royalty arrangements.
  • Patent Challenges: Broad claims may be vulnerable to invalidation challenges based on prior art; narrow claims can limit enforceability.

Conclusion

AU2008358027 embodies a focused innovation within the pharmaceutical patent landscape, particularly emphasizing specific compositions or methods associated with therapeutic applications. Its scope, defined primarily by its claims, encompasses a spectrum from broad composition claims to more specific method or delivery system claims. Evaluating this patent requires a careful review of claim language, prior art, and competitive patents.


Key Takeaways

  • Scope Precision: The patent’s strength depends on how reads the claims; broader claims confer stronger exclusivity but are more vulnerable to invalidation.
  • Landscape Positioning: The patent likely exists within a dense environment of similar pharmaceutical patents; thorough freedom-to-operate analysis is critical.
  • Strategic Implication: Innovationspecific claims suggest targeted protection, but competitors may design around narrower elements.
  • Legal Challenges: Broad or vague claims increase the risk of litigation or invalidation; narrow but well-supported claims enhance enforceability.
  • Commercial Relevance: The patent secures a competitive edge in the Australian market, subject to ongoing patent protections and potential challenges.

FAQs

1. What is the primary inventive concept in AU2008358027?
The patent likely involves a novel pharmaceutical composition, formulation, or method of treatment involving specific active ingredients or delivery mechanisms tailored for particular therapeutic indications.

2. How broad are the claims of AU2008358027?
While exact claim language is necessary for precise assessment, the patent probably encompasses both broad composition claims and narrower method or delivery system claims, influencing its enforceability and infringement scope.

3. What is the significance of this patent within the global pharmaceutical landscape?
Its significance depends on the novelty of the active ingredients and formulations, and whether similar patents exist internationally. It potentially protects a unique Australian commercial interest while aligning with global patent strategies.

4. Can competitors design around the claims of this patent?
Yes, if the claims are narrowly defined, competitors might develop alternative formulations or methods that do not infringe. Broad claims, however, challenge such workaround strategies.

5. How does this patent impact licensing and market exclusivity?
It provides exclusive rights within Australia, allowing patent holders to license the invention and prevent unauthorized commercial use, bolstering market position and revenue.


References

  1. Australian Patent AU2008358027 Filing and Grant Details.
  2. Patent Classification and Patent Landscape Analyses (PatentScope, Espacenet).
  3. Australian Patent Office Guidelines for Examination and Claims Interpretation.
  4. Prior Art Publications and Related Patent Applications in the Therapeutic Area.

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