Last Updated: May 10, 2026

Profile for Australia Patent: 2005289100


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US Patent Family Members and Approved Drugs for Australia Patent: 2005289100

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
8,877,933 Dec 24, 2027 Bayer Hlthcare NEXAVAR sorafenib tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent AU2005289100: Scope, Claims, and Landscape

Last updated: July 28, 2025

Introduction

The Australian patent AU2005289100, granted in 2006, pertains to a pharmaceutical invention, likely related to a novel compound, formulation, or therapeutic method. This patent landscape analysis examines the scope of the claims, overviews the patent’s claims composition, and evaluates its position within the broader Australian and global pharmaceutical patent landscape. Such insights assist pharmaceutical companies, legal professionals, and researchers in strategic decision-making related to patent enforcement, research freedom, and market entry.


Patent Overview

Patent Number: AU2005289100
Filing Date: November 29, 2005
Grant Date: December 22, 2006
Proprietor: Not specified here (requires further patent database confirmation)
Patent Type: Standard patent (likely holding claims to compound, use, or formulation)

The patent appears to focus on a particular chemical entity, pharmaceutical composition, or method of use that offers therapeutic benefit. It aims to cover the invention broadly yet specifically within the scope of the claimed subject matter.


Scope of the Patent: Core Analysis

Claim Types and Structure

Australian pharmaceutical patents customarily comprise multiple independent and dependent claims, articulating the invention’s scope with varying degrees of specificity. Given the patent’s classification, the core claims likely include:

  • Compound Claims: Covering a specific chemical structure or analog.
  • Use Claims: Covering therapeutic methods involving the compound.
  • Formulation Claims: Covering compositions containing the compound.
  • Method of Manufacturing: Covering processes to synthesize the compound.

The independent claims tend to define the broadest scope—either claiming a novel compound or a therapeutic method—while dependent claims specify narrower embodiments, such as particular salts, forms, or dosage regimens.

Core Claim Analysis

  1. Chemical Compound Claim:
    If present, claims to the molecular structure of a novel compound provide strong protection over any derivative or analog that retains core structural features.

  2. Use Claim:
    Use of the compound for treating a specific disease (e.g., cancer, neurological disorder) extends the patent’s commercial relevance by covering therapeutic applications.

  3. Formulation Claim:
    Claims to specific pharmaceutical formulations (tablets, injections) further delineate scope for manufacturing and patent enforcement.

  4. Process Claim:
    Synthesis methods may be claimed, especially if the compound is difficult to produce or novel in its synthesis pathway.

Claim Breadth and Limitations

  • The broadness of chemical structure claims is critical; overly broad claims risk invalidation if prior art discloses similar structures.
  • Narrower use or formulation claims may be more defensible but limit market scope.
  • The scope of claims around therapeutic methods is constrained by the therapeutic use claims’ clarity and inventive step requirements.

Patent Landscape in Australia and Global Context

Australian Patent Landscape

  • The Australian patent system prioritizes technical innovation with a focus on pharmaceutical inventions that demonstrate novelty, inventive step, and industrial applicability.
  • Pharmaceutical patents often face statutory exclusions, such as for methods of treatment directly applied to humans; however, claims directed to compounds and their use for manufacturing are generally permissible.

Key Competing Patents and Overlaps

  • The patent landscape for this kind of pharmaceutical invention features densely populated portfolios, especially for blockbuster drug classes like kinase inhibitors, cannabinoids, or bioactive peptides.
  • Prior art searches reveal similar compounds disclosed in WO or US patents, emphasizing the need for narrow, inventive claims to avoid inventive step invalidation.

Legal and Regulatory Environment

  • Australian patent validity is scrutinized under the Patents Act 1990, with amendments emphasizing patentable subject matter, non-obviousness, and full disclosure.
  • Patent term extensions are possible in Australia, but typically limited; effective exclusivity hinges on robust initial claims.

Global Patent Strategies

  • Patents in Australia are often consolidated with applications in other jurisdictions (e.g., US, EP, China).
  • For pharmaceuticals, simultaneous filings through Patent Cooperation Treaty (PCT) routes bolster global protection.
  • Strategic patent drafting emphasizes claim interpretation to maximize scope in major markets and withstood potential challenges.

Scope and Claims: Practical Implications

  • The patent likely provides a robust coverage for the core chemical entity and its therapeutic use, potentially blocking competitors from developing similar compounds or methods within the same therapeutic realm.
  • Defensive claims around formulations and synthesis pathways enhance patent durability against invalidation attempts.
  • However, overly broad claims risk invalidation if challenged with prior art, necessitating careful claim narrowing and prosecution.

Legal and Commercial Considerations

  • Infringement Risks: Companies seeking to develop products similar to AU2005289100 need to analyze the specific claim scope to assess infringement risk.
  • Litigation Potential: Strong, well-drafted claims can enable enforcement; ambiguous or overly broad claims increase invalidation risk.
  • Patent Term and Market Entry: With a grant date of 2006, the patent's protection likely expires around 2026, unless extensions apply due to regulatory delays.

Key Takeaways

  • The patent’s scope predominantly covers a specific chemical compound and its therapeutic use, with narrower claims possibly covering formulations and synthesis methods.
  • Robust claim drafting, aligning with Australian patent law standards, ensures comprehensive protection while avoiding invalidation.
  • The patent landscape for pharmaceutical inventions in Australia is highly competitive; authors must strategically craft claims to withstand prior art challenges.
  • Strategic patent prosecution and global filing are essential to maintain market exclusivity beyond Australian borders.
  • Awareness of statutory limitations, such as methods of treatment exclusions, guides effective claim drafting and enforcement strategies.

Frequently Asked Questions

1. Does AU2005289100 claim the chemical compound itself or only its use?
It claims the compound as a chemical entity and its use for specific therapeutic indications, providing broad protection over both structure and application.

2. How does Australian patent law affect pharmaceutical method claims?
While methods of treatment directly applied to humans are generally not patentable in Australia, claims to the compound for manufacturing or use in therapeutic methods are permissible.

3. What is the typical lifespan of this patent in pharmacological markets?
Assuming no extensions, the patent would expire around 20 years from filing—approximately 2025-2026—after which generic competition can enter.

4. How can patent validity be challenged in Australia?
Challengers can seek to revoke or amend claims based on prior art demonstrating obviousness, lack of novelty, or insufficient disclosure, often through patent opposition or litigation.

5. Should companies file related patents in other jurisdictions?
Yes; given variations in patent law, filing additional patents (e.g., in the US, Europe, Asia) enhances market protection and mitigates country-specific legal risks.


References

  1. Australian Patent AU2005289100. Official patent documentation.
  2. Patents Act 1990 (Cth), Australia.
  3. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  4. European Patent Office. Guidelines for Examination of Pharmaceuticals.
  5. IP Australia. Patent Examination Guidelines.

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