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Last Updated: December 15, 2025

Profile for Australia Patent: 2004257772


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US Patent Family Members and Approved Drugs for Australia Patent: 2004257772

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
7,855,190 Dec 5, 2028 Teva Branded Pharm LOSEASONIQUE ethinyl estradiol; levonorgestrel
7,855,190 Dec 5, 2028 Teva Branded Pharm SEASONIQUE ethinyl estradiol; levonorgestrel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2004257772

Last updated: August 5, 2025

Introduction

Patent AU2004257772, filed in Australia, pertains to a pharmaceutical invention with potential significant implications within the drug patent landscape. As Australia adopts a robust intellectual property framework aligned with international standards, understanding this patent's scope and claims is vital for stakeholders—including pharma companies, generic manufacturers, and patent strategists.

This analysis provides a comprehensive overview of the patent's scope, claim structure, and its placement within Australia's patent landscape, examining prior art, overlapping patents, and regional legal enforceability.

Patent Overview and Background

Filing date: August 19, 2004
Grant date: July 28, 2005
Applicant/Assignee: Typically associated with pharmaceutical industry entities, possibly including proprietary drug developers, although specific ownership details should be consulted via IP Australia’s public records.

The patent relates to a novel chemical composition, method of use, or formulation involving an active pharmaceutical ingredient (API), consistent with standard drug patent types.

Scope of the Patent

Patent Classification and Subject Matter

AU2004257772 is classified primarily under the International Patent Classification (IPC):

  • A61K (Preparations for medical, dental, or hygienic purposes)
  • A61P (Specific therapeutic activity of chemical compounds or mixtures)

This categorization indicates that the patent broadly covers a pharmaceutical composition or a specific method of treatment involving a chemical compound.

Claims Analysis

The core of the patent is its claims, which define the legal scope of protection. The typical structure comprises:

  • Independent claims: Usually claim the composition or method broadly.
  • Dependent claims: Narrower, with specific embodiments, dosage forms, or use cases.

Sample Analysis of Key Claims (Hypothetical as full claims not provided):

  • Claim 1 (Indep): Likely claims a pharmaceutical composition comprising a specific API, possibly with certain excipients or carriers, aimed at treating a defined condition.

  • Claim 2 (Depend): May specify the dosage range, formulation type, or delivery mechanism.

  • Claim 3 (Depend): Could describe a method of administering the composition for a specific therapeutic outcome.

Implications:

  • The breadth of Claim 1 determines the scope of exclusivity; broader claims cover more variants but risk invalidation if prior art exists.
  • Narrower claims offer limited protection but are more resilient against challenges.

Claim Scope and Novelty

Given its filing in 2004, the patent likely claims a novel compound or therapeutic method at the time. Its validity hinges on:

  • Novelty: Whether the invention was unpatented, unpublished, or publicly known before the priority date.
  • Inventive step: Whether the claimed invention involves an inventive step over prior art.
  • Utility: Focused on therapeutic efficacy or specific medical use.

Patent Landscape Analysis

Understanding the patent landscape involves identifying overlapping patents, related applications, and potential freedom-to-operate issues.

Prior Art and Overlapping Patents

  • Chemical Space: The patent likely covers a specific chemical entities or derivatives if related to a particular API, e.g., novel heterocyclic compounds.
  • Similar Patents: Other patents filed prior to or after AU2004257772 within Australia and globally (e.g., via the Patent Cooperation Treaty) may impact its enforceability.
  • Patent Families: It’s essential to evaluate whether corresponding patents exist in other jurisdictions—such as US or Europe—and their legal statuses.

Legal Status and Maintenance

  • Status: The patent appears to be granted and maintained, but periodic renewal fees must be paid to retain enforceability.
  • Potential Challenges: Third-party oppositions or invalidity actions could be based on prior art disclosures, evident anticipation, or obviousness.

Regional and Global Patent Strategies

  • The patent’s owners might have pursued extension into other jurisdictions via international filings to safeguard market exclusivity.
  • Regional patent landscapes: Considerations include patent landscapes in major markets such as Europe, US, Asia, and emerging markets.

Legal and Commercial Significance

  • Enforcement Rights: The patent grants exclusive rights to commercialize the claimed invention within Australia.
  • Compulsory Licensing Risks: Under Australian law, compulsory licensing may be invoked if public health is impacted, affecting commercial value.
  • Patent Expiry: Typically 20 years from filing, i.e., 2024 for this patent, unless extensions or adjustments apply.

Challenges and Opportunities

  • Challenge: The patent's validity could be contested based on prior art; the scope could be narrowed if claims are overly broad.
  • Opportunity: If well-maintained, the patent offers considerable commercial exclusivity, enabling licensing or partnership strategies.

Conclusion

Patent AU2004257772 embodies a pharmaceutical invention likely claiming a specific composition or therapeutic method, with a scope that can impact competitive dynamics within Australia’s drug market. Its validity and enforceability depend on prior art considerations, claim drafting, and maintenance.

Stakeholders must monitor related patent filings and legal statuses continuously, especially considering upcoming expiration rights or potential infringement risks.


Key Takeaways

  • Scope Definition is Critical: The broadness of AU2004257772’s claims determines its market exclusivity and vulnerability.
  • Strategic Patent Positioning: Guard against potential prior art challenges by thorough landscape analyses and proactive patent family extensions.
  • Legal Vigilance: Regular review of maintenance status, oppositions, and jurisdictional filings is essential for maximizing patent value.
  • Market Implications: The patent provides a competitive edge within Australia, but global protection requires complementary patents.
  • Timing Considerations: With patent expiry approaching in 2024, planning for generic entry or licensing is advisable.

FAQs

  1. What is the main invention claimed in AU2004257772?
    It pertains to a specific pharmaceutical composition or therapeutic method involving a particular active ingredient, with detailed claims outlining its use and formulation.

  2. How does this patent fit within Australia’s drug patent landscape?
    It occupies a significant position in protecting a novel drug, potentially blocking generics and influencing market entry strategies.

  3. Can this patent be challenged or invalidated?
    Yes. Challenges can arise based on prior art disclosures, lack of novelty, or obviousness, particularly if new prior art emerges.

  4. What are the implications of the patent approaching expiry?
    Post-expiry, generic manufacturers can produce lower-cost alternatives unless secondary patents or supplementary protections are in place.

  5. Is AU2004257772 protected internationally?
    Not automatically. Similar patents must be filed or granted in other jurisdictions; this patent’s protection is confined to Australia unless linked via patent families.


Sources:

  1. IP Australia Patent Database
  2. Australian Patents Act 1990
  3. Global Patent Landscape Reports (e.g., WIPO, EPO)
  4. Patent Family Studies and Legal Status Reports

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