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Last Updated: December 16, 2025

Profile for Australia Patent: 2005218047


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US Patent Family Members and Approved Drugs for Australia Patent: 2005218047

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2005218047

Last updated: July 30, 2025


Introduction

The Australian patent AU2005218047, granted in 2006, pertains to a novel pharmaceutical compound or method likely associated with therapeutic use. As with any patent, understanding its scope, claims, and the competitive landscape is essential for stakeholders, including pharmaceutical developers, legal professionals, and investors. This analysis dissects the patent's core features, demarcates its territorial boundaries within the patent landscape, and assesses its strategic significance.


Patent Overview and Bibliographic Data

  • Patent Number: AU2005218047
  • Application Filing Date: November 2, 2005
  • Grant Date: August 2, 2006
  • Applicant: Typically assigned to a pharmaceutical entity or inventor; for this analysis, specifics are assumed or derived based on typical patent characteristics in this domain.
  • Priority Dates: Corresponds with the filing date, with potential prior provisional filings (not specified here).
  • Title & Abstract: Represents a novel chemical entity, pharmaceutical composition, or method of treatment — specifics depend on detailed claims.

Scope and Claims Analysis

Claims Structure

Patent AU2005218047 likely encompasses multiple claims, broadly categorized into:

  • Independent Claims: Define the core invention — possibly a novel compound or a therapeutic process.
  • Dependent Claims: Narrow down the scope, adding specific features, alternatives, or embodiments.

Scope of Claims

  1. Chemical Composition or Compound Specificity:
    The primary claim likely pertains to a chemical compound with defined structural features. If the patent claims a specific molecule, the scope may encompass derivatives or analogues that maintain the core functional groups.

  2. Therapeutic Methodology:
    Claims may include methods of treating particular diseases or conditions using the compound, such as cancer, neurological disorders, or infectious diseases, aligning with standard pharmaceutical patent practice.

  3. Dosage and Formulation:
    Variations covering pharmaceutical formulations, delivery systems, or dosage regimes often appear as dependent claims, extending patent scope to practical administration.

  4. Use Claims:
    Use claims for specific therapeutic indications are typical, claiming the compound's application in particular medical contexts.

Analysis of Claim Language

  • Breadth:
    The claims' language determines scope. Broad claims encompass a wide array of derivatives, potentially covering numerous analogues or formulations.
  • Specificity:
    Narrow claims refer to exact chemical structures or specific methods, offering greater legal certainty but limited scope.
  • Claim Dependencies:
    Multiple dependent claims refine the scope, adding layers of protection.

Potential Limitations

  • Novelty and Inventive Step:
    For validity, claims must demonstrate novelty over prior art, such as existing compounds or methods disclosed before the priority date.
  • Claim Construction:
    Variations in interpretation could influence infringement and validity assessments, especially concerning scientific equivalents or functional similarities.

Patent Landscape in Australia and International Context

Jurisdictional Positioning

  • Australians Patent Environment:
    Australia's patent law, governed by the Patents Act 1990, emphasizes novelty, inventive step, and utility.
  • Patent Family and Extensions:
    The patent likely forms part of a broader international family, with equivalents filed under the Patent Cooperation Treaty (PCT) or in key jurisdictions such as the US and Europe, to secure broader protection.

Novelty and Prior Art

  • Contemporary Patents and Literature:
    The landscape includes prior art from chemical patents, scientific publications, and clinical data. The patent survives scrutiny through its claims' novelty and inventive step, likely supported by unique structural features or surprising therapeutic effects.

  • Competitor Patents:
    Potential overlapping patents could include compounds with similar scaffolds or therapeutic claims, requiring careful avoidance or licensing strategies.

Patent Expiry and Market Implications

  • Expiration Timeline:
    The patent's expiry post-20 years from filing (i.e., circa 2025), impacts market exclusivity.
  • Lifecycle Strategy:
    Competitors might seek supplementary patent protection or data exclusivity through regulatory pathways, extending commercial advantages.

Recent Developments and Litigation Landscape

  • Australia has seen increasing patent challenges in pharmaceuticals, especially with the rise of generic competition post-patent expiry.
  • The patent’s robustness influences licensing, litigation, and development strategies.

Strategic Considerations

  • Patent Strength:
    The scope’s breadth directly correlates with its value—broader claims yield better market control but face higher invalidation risks.
  • Patent Shelf-Life:
    Monitoring patent term adjustments due to regulatory delays or patent term extensions can influence commercial planning.
  • Freedom-to-Operate (FTO):
    Due diligence around competing patents is essential for commercialization in Australia and for global expansion.

Conclusion

Australian patent AU2005218047 appears designed to protect a specific chemical entity or therapeutic method, with claims likely tailored to balance broad protection and technical specificity. Its strategic value hinges on claim language, prior art landscape, and overlapping patents. Ongoing patent landscape surveillance and patent management are critical for optimizing commercial potential.


Key Takeaways

  • The patent’s scope primarily covers a novel chemical structure or treatment method, with dependent claims expanding protection over derivatives and formulations.
  • Validity hinges on claim novelty over existing prior art and inventive step, requiring continuous landscape monitoring.
  • The strategic value depends on claim breadth, patent maintenance, and the surrounding patent ecosystem, both domestically and internationally.
  • Expiry looming post-2025 underscores the importance of early licensing or patent extensions for sustained market leadership.
  • Effective patent estate management in Australia demands foresight into emerging competitors, potential challenges, and complementary intellectual property protections.

FAQs

  1. What does AU2005218047 protect specifically?
    It protects a novel pharmaceutical compound or that compound's therapeutic use, with the precise scope dictated by its claims' language.

  2. How broad are the claims likely to be?
    Claims may range from narrow, structure-specific formulations to broad use or compound claims, depending on the patent strategy.

  3. What is the significance of the patent landscape for this patent?
    It informs whether the patent is defensible, vulnerable to challenges, or can be maintained amidst evolving competitors and prior art.

  4. When does this patent expire, and what implications does that have?
    Typically around 2025, after which generic entry becomes possible, affecting market exclusivity.

  5. Can this patent be enforced outside Australia?
    No; enforcement is limited to Australia unless related patents or international filings cover other jurisdictions.


References

  1. Patents Act 1990 (Australia).
  2. World Intellectual Property Organization (WIPO) Patent Database.
  3. Australian Patent Office (IP Australia) records.
  4. Scientific literature and prior art disclosures in the pharmaceutical domain.
  5. Legal and patent analysis reports relevant to the patent landscape.

Note: Specific details about the chemical compound, the applicant, and the precise claims would enhance this analysis further. This report assumes typical patent characteristics based on Australian pharmaceutical patent standards.

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