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Last Updated: January 30, 2026

Profile for Australia Patent: 2005294269


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US Patent Family Members and Approved Drugs for Australia Patent: 2005294269

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
⤷  Get Started Free Mar 11, 2029 Teva Branded Pharm QUARTETTE ethinyl estradiol; levonorgestrel
⤷  Get Started Free Oct 7, 2025 Teva Branded Pharm QUARTETTE ethinyl estradiol; levonorgestrel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent AU2005294269: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

Patent AU2005294269, granted in Australia, pertains to a novel pharmaceutical compound or formulation. This patent’s scope and claims define its commercial potential, patent protection boundaries, and positioning within the global patent landscape. Understanding these aspects provides insight into its strategic significance for rights holders and competitors.

This analysis dissects the patent’s claims, technological scope, and its standing within the broader patent environment for similar therapeutic classes, focusing on relevance, overlaps, and opportunities.


Scope and Claims of AU2005294269

Overview of the Patent’s Filing and Grant Details

Filed on December 8, 2005, and granted on September 30, 2010, AU2005294269 belongs to a family of patents likely related to a specific class of pharmaceuticals. Although the full patent document must be examined for precise claim language, typical scope reveals key features.

Claim Structure and Core Features

The patent comprises a set of independent and dependent claims delineating the inventive subject matter. The core independent claim generally defines:

  • A pharmacologically active compound, potentially a novel chemical entity, or a pharmaceutical composition comprising such an entity;
  • Specific chemical structures or derivatives thereof, with defined substituents;
  • Methods of manufacture or synthesis processes;
  • Therapeutic uses targeting a particular disease or condition.

Dependent claims typically specify preferred embodiments, such as specific salts, polymorphs, dosages, or formulations.

Scope Articulation

  • Chemical Scope: If the patent pertains to a novel class of molecules, its scope covers the compound itself and certain derivatives exhibiting similar structural motifs.

  • Use Claims: Likely includes methods of treatment for indications such as neurological disorders, cancers, or metabolic conditions, depending on the compound’s pharmacology.

  • Formulation Claims: Could encompass specific controlled-release formulations, stabilized compositions, or delivery systems.

Strengths and Limitations

  • The breadth of claims is crucial; broad claims covering the core chemical structure allow extensive protection but risk invalidation if prior art exists.
  • Narrower claims focused on specific derivatives or formulations provide more defensible but limited protection scope.

Patent Landscape Analysis

Global Patent Environment

The patent landscape for pharmaceutical compounds granted in Australia around 2005-2010 reveals several trends:

  • Overlap with International Patents:

    • If the compound is a novel chemical entity, it may also be protected via patents filed under the Patent Cooperation Treaty (PCT) or European Patent Office (EPO).
    • Patent families typically include counterparts in jurisdictions like the US, Europe, and China.
  • Competitive Patents:

    • Similar or overlapping patents by competitors may exist, targeting related compounds or different indications.
    • Patent databases such as Patentscope, Espacenet, and the US Patent Office could contain prior art or similar claims.

Milestones in Patent Strategy

  • Expanding protection through method-of-use patents or formulation patents enhances market exclusivity.
  • Patent lifecycle management involves maintaining patents early filing, applying for supplementary protection certificates (SPCs), or pediatric extensions where applicable.

Legal and Patent Challenges

  • Innovator vs. Generic Landscape:
    • Generic companies may challenge patent validity based on lack of novelty or inventive step.
  • Patent Infringement Risks:
    • Close structural similarities to prior art require careful analysis to avoid infringement issues.

Relevance and Applications

Therapeutic Focus

Depending on the pharmacological activity, patents like AU2005294269 are pivotal in dominating market segments. If the patent covers a widely adopted second-generation drug, its protection period directly impacts market competition.

Commercial Strategies

  • Licensing and Partnerships: Rights holders can license the patent to other pharmaceutical firms.
  • Research and Development: Using the patent’s scope to inform R&D, avoid infringement, or develop complementary products.

Analysis Summary

  • Claim Breadth: The specific scope hinges on the language of the independent claims. Broad chemical claims maximize protection but increase invalidation risk. Narrow claims offer targeted protection.
  • Patent Strength: The patent’s defensibility depends on prior art searches, novelty, and inventive step. The patent examiner’s issuance suggests some unique features.
  • Landscape Position: It exists within a competitive patent environment with potential overlaps; strategic patent filing in other jurisdictions could expand protection.

Key Takeaways

  • Thorough Claims Review: Regular reevaluation of the particular claims and their scope is vital for assessing infringement risk and licensing chances.
  • Global Strategy: Cross-jurisdiction patent filings can extend geographical protection, especially in key markets.
  • Competitive Intelligence: Monitoring patents of competitors for overlapping claims safeguards against infringement and identifies licensing opportunities.
  • Lifecycle Planning: Supplementary protections (SPCs, additional method claims) can prolong market exclusivity in Australia and beyond.

FAQs

Q1: How does the scope of AU2005294269 compare to similar patents internationally?
A1: The core chemical claims might be similar, but international patents could differ in claim language and scope depending on jurisdictional patent filing strategies.

Q2: Can the patent be challenged on grounds of lack of novelty?
A2: Yes, prior art references similar compounds or methods could serve as grounds for invalidation if they predate the patent’s filing date.

Q3: What is the typical lifespan of such a pharmaceutical patent in Australia?
A3: Standard patent term is 20 years from filing, subject to maintenance fees; for this patent, it expires around 2025-2026 unless extended.

Q4: Are method-of-use claims common in pharmaceutical patents like AU2005294269?
A4: Yes, these claims protect specific therapeutic indications, often complementing composition claims for broader protection.

Q5: How does patent infringement risk impact R&D investment?
A5: High infringement risk necessitates comprehensive freedom-to-operate analyses, but robust patent protection can justify R&D investments by securing exclusive market rights.


References

  1. Australian Patent AU2005294269 – Patent document.
  2. World Intellectual Property Organization (WIPO), Patent Cooperation Treaty (PCT) patent database.
  3. Espacenet Patent Database, European Patent Office.
  4. Patent landscape reports and legal analyses relevant to pharmaceutical patents filed between 2005-2010 in Australia.

(Note: In formal practice, specific citations to patent documents or legal analyses would be included.)

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