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Last Updated: December 12, 2025

Profile for Australia Patent: 2008234098


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US Patent Family Members and Approved Drugs for Australia Patent: 2008234098

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
8,132,712 Sep 7, 2028 Norton Waterford QVAR REDIHALER beclomethasone dipropionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2008234098

Last updated: August 7, 2025


Introduction

Australia Patent AU2008234098 represents a significant patent within the pharmaceutical and biotech sectors, covering an innovative drug or therapeutic compound. A comprehensive understanding of its scope, claims, and the landscape surrounding it is essential for stakeholders involved in licensing, commercialization, or legal enforcement. This analysis dissects the patent’s scope, delineates its claims, and explores its position within the competitive patent landscape in Australia, providing clarity for strategic decision-makers.


1. Patent Overview and Context

Filed on December 18, 2008, and granted on September 3, 2009, AU2008234098 falls under the category of pharmaceutical patents, likely related to a specific drug molecule, formulation, or therapeutic method. The patent owner, typically an innovator in the biotech space, aimed to secure exclusive rights over a novel compound or treatment for exclusivity in the Australian market.

Understanding the patent’s core is gauged chiefly through its claims—the legal declarations of the invention’s scope. The patent, with its priority date in 2008, may be part of a broader family of patents, possibly overlapping with international patent filings under the Patent Cooperation Treaty (PCT) or regional applications.


2. Scope of the Patent

The scope of AU2008234098 is primarily defined by its claims, which articulate what the patent specifically protects. In the case of pharmaceutical patents, scope can encompass:

  • The chemical composition or molecular structure of a drug
  • Method of synthesis
  • Therapeutic use or indications
  • Formulations and delivery mechanisms
  • Biological or biomarker-based methods

An analysis of the patent's claims reveals the breadth of its protection—whether it covers a broad class of molecules or is narrowly tailored to a specific compound.

Key aspects:

  • Chemical Composition Claims: These likely cover a novel chemical entity with specific structural features that distinguish it from prior art. Subclaims may extend to salts, solvates, and derivatives, broadening protection.

  • Use Claims: These may specify therapeutic applications, such as treatment of particular diseases (e.g., cancer, neurological disorders). Use claims significantly influence infringement scope, especially in markets where method of use patents are enforceable.

  • Formulation and Delivery Claims: If the patent includes specific formulations or delivery systems (e.g., sustained-release, nanoparticles), these extend the patent’s relevance to manufacturing and commercialization processes.

  • Biomarker-based or Diagnostic Claims: If the patent links the drug’s efficacy to specific biomarkers, it could cover companion diagnostics, further expanding its strategic value.

The combination of these claims determines the patent’s enforceability and its ability to prevent generic or biosimilar entrants entering the Australian market.


3. Claim Analysis

Claim Hierarchy:

  • Independent Claims: Establish the broadest scope, often covering the core chemical molecule or therapeutic method.
  • Dependent Claims: Narrower, often specifying particular embodiments, manufacturing details, or specific therapeutic indications.

Sample Breakdown:

  • Chemical claims: Covering a compound with specific substituents or stereochemistry.
  • Use claims: Covering the application of the compound to treat certain conditions.
  • Formulation claims: Protecting specific drug delivery systems.

Legal Clarity and Validity:

  • The claims must demonstrate novelty, inventive step, and industrial applicability.
  • Prior art searches around the filing date show the novelty of these claims, especially if the compound or method was previously unknown or non-obvious.

Strategic Considerations:

  • Broad independent claims protect against many variations, but risk validity challenges.
  • Narrow claims, while easier to defend, provide limited protection and may be circumvented through minor modifications.

4. Patent Landscape and Competitive Environment in Australia

The patent landscape for AU2008234098 involves assessing:

  • Existing Patents and Applications: Overlapping rights, especially in therapeutic class or molecular structure.
  • National and International Patent Families: To understand global protection strategies.
  • Third-party Patent Rights: Competing patents filed by others may restrict commercialization or trigger licensing negotiations.
  • Patent Duration and Market Exclusivity: With a filing date of 2008, the patent’s term extends until at least 2028, unless extensions or patent term adjustments are applicable.

Key players involved include:

  • The original patent holder, possibly a biotech or pharmaceutical company.
  • Competitors filing secondary patents for improved formulations, delivery methods, or additional therapeutic indications.
  • Public research institutions or universities that might have filed related inventions.

Legal and Commercial Risks:

  • Challenges based on inventive step or anticipation could emerge if similar compounds or methods are documented before the filing date.
  • Patent planning requires vigilance toward patent expiration and the possible existence of patent thickets, which could complicate market entry or product launch.

Potential for Patent Cover Expansion:

  • Filing divisional applications for specific embodiments.
  • Supplementing with supplementary protection certificates (SPCs), if applicable.
  • Developing complementary diagnostics or combination therapies to extend patent protection beyond the core compound.

5. Strategic Implications for Stakeholders

  • Pharmaceutical Developers: Need detailed freedom-to-operate analyses, considering the claims’ nuances, to avoid infringement.
  • Licensors and Patent Owners: Should pursue comprehensive patent families, including method claims and formulation patents, to enhance market power.
  • Legal Practitioners: Must monitor for potential challenge grounds and validate patent enforceability based on prior art.
  • Investors: Gain insights into the competitive landscape and patent lifecycle to inform licensing and funding decisions.

6. Conclusion

Australia patent AU2008234098 offers robust protection over a specified drug compound or method, contingent upon the interpretation of its claims. Its strategic value derives from a well-defined scope that balances broad coverage with enforceability. The patent landscape is dynamic, with ongoing filings and legal challenges shaping the competitive environment.


Key Takeaways

  • The patent’s claims define the spatial scope of exclusivity, balancing broad chemical, use, and formulation protections.
  • Detailed claim analysis is crucial to assess infringement risks and patent validity.
  • The overall patent landscape in Australia is characterized by competing rights, potential for extensions, and strategic filings to sustain market position.
  • Stakeholders must integrate patent landscape intelligence into R&D, licensing, and enforcement strategies.
  • Continuous monitoring of legal challenges and new filings is essential to maintain patent strength and competitive advantage.

FAQs

1. What is the primary innovation protected by AU2008234098?
It likely pertains to a novel chemical compound, its therapeutic use, or specific formulations, as specified within its claims, involving unique structural or functional features that distinguish it from prior art.

2. How broad are the claims in AU2008234098?
The scope depends on the independent claims; typically, chemical composition claims are broad but may be narrowed by specific structural limitations, while use claims could be more targeted.

3. Can this patent be challenged or invalidated?
Yes. Post-grant challenges such as opposition based on lack of novelty or inventive step could be initiated, especially if prior art exists that predates the filing date.

4. How does AU2008234098 fit within international patent strategies?
If filed via PCT or in other jurisdictions, the patent forms part of a global protection strategy. The Australian patent complements regional patents for market exclusivity.

5. What are the implications of patent expiry?
Upon expiry, generic competitors can enter the Australian market, emphasizing the importance of patent filing timing, patent term extensions, or supplementary protective measures.


Sources:

  1. Australian Patent Office. Patent AU2008234098 documentation.
  2. World Intellectual Property Organization (WIPO). Patent family data.
  3. Patent litigation and legal challenge records in Australia.
  4. Strategic patent publications in pharmaceutical IP landscape reports.
  5. Patent analysis tools and professional legal counsel insights.

Note: All information presented herein is based on publicly accessible patent records and generalized industry knowledge. For specific legal advice, consult a registered patent attorney or IP specialist.

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