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Last Updated: December 18, 2025

Profile for Australia Patent: 366507


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US Patent Family Members and Approved Drugs for Australia Patent: 366507

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 Nov 21, 2032 Mayne Pharma BIJUVA estradiol; progesterone
⤷  Get Started Free Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
⤷  Get Started Free Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
⤷  Get Started Free Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
⤷  Get Started Free Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Australian Patent AU366507: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

Patent AU366507, granted by the Australian Patent Office, pertains to a specific pharmaceutical compound or formulation. This analysis explores the scope and claims of AU366507 to clarify its patent coverage, evaluates its position within the Australian patent landscape, and assesses potential implications for competitors, patent holders, and the pharmaceutical industry.


Patent Overview and Basic Metadata

  • Patent Number: AU366507
  • Grant Date: [Insert Date — e.g., 23 March 2014]
  • Applicant/Assignee: [Typically a pharma company or individual—details to be specified based on official records]
  • Field: Pharmaceutical composition or active ingredient patent (exact subject matter required from the specification)

Note: The comprehensive understanding of the patent’s scope hinges on precise claims and description details, which define enforceability and competitive boundaries.


Scope of Patent AU366507

The scope of AU366507 fundamentally depends on its claims, which delineate the borders of the patent monopoly. In pharmaceutical patents, scope typically encompasses the active compound(s), formulations, uses, methods of manufacture, and applicable dosage forms.

1. Core Claims Analysis:

  • The primary claims likely specify a novel chemical entity or a novel use of an existing compound.
  • Claims may also define unique combinations of active ingredients, novel formulations, or delivery mechanisms.
  • The claims probably extend to methods of synthesis or manufacturing processes.

2. Claims Hierarchy:

  • Independent Claims: These typically establish broad patent coverage, e.g., claiming a compound or therapeutic use.
  • Dependent Claims: These refine and narrow the scope to specific embodiments, such as specific substituents, dosages, or formulations.

3. Claim Language and Interpretation:

  • The scope depends on claim language – whether it defines a broad class of compounds or a specific compound.
  • Use of language like “comprising,” “consisting of,” and “wherein” influences breadth.
  • For example, a claim stating “a compound of formula I” covers all compounds fitting the structure, whereas “a pharmaceutical composition comprising compound I” covers formulations containing that compound.

4. Effect of Description and Specification:

  • The patent’s description clarifies the embodiments, enabling proper claim interpretation.
  • Disclosures of synthesis methods, data supporting efficacy, and specific examples bolster the enforceability of claims.

Claims Analysis and Key Points

Without access to the current official claims, typical features include:

  • Novel Chemical Entity: For instance, if AU366507 covers a new class of molecules targeting a particular receptor—claims would encompass the chemical structure, derivatives, and salts.
  • Therapeutic Use Claims: Cover intervention methods, e.g., treatment of specific diseases such as cancer or neurological conditions.
  • Formulation and Manufacturing Claims: Encompassing unique compositions or techniques enhancing stability, bioavailability, or delivery.
  • Combination Claims: Involving co-administration with other drugs or compounds.

Note: The patent’s enforceability hinges on claim clarity, novelty, and inventive step, as per Australian patent law standards [1].


Patent Landscape in Australia

1. Patent Family and Priority Data:

  • If AU366507 originates from an international priority (e.g., PCT), it likely forms part of a broader patent family.
  • An analysis reveals potential overlaps with patents in other jurisdictions, providing strategic leverage or risk.

2. Prior Art and Patent Validity:

  • Pre-existing art related to similar compounds or methods might impact validity.
  • The patent office’s examination process assesses novelty, inventive step, and industrial applicability based on existing disclosures.

3. Competing Patents & Freedom to Operate:

  • Several patents may establish overlapping claims in the same therapeutic area, complicating commercialization.
  • Patent landscapes often contain "patent thickets"—clusters of overlapping patents—that restrict market entry unless carefully navigated.

4. Patent Expiry and Market Dynamics:

  • AU366507’s expiry date generally provides exclusivity for 20 years from the priority date, influencing market monopolies.

5. Patent Litigation & Litigation Risks:

  • The position and strength of AU366507 relative to other patents determine litigation risks, especially if similar compounds or uses are patented elsewhere.

6. Patent Strategies in Australia:

  • Filing nationwide and with international pathways (e.g., PCT) ensure broader protection, but patent drafting must be rigorous to withstand legal scrutiny.

Implications and Strategic Considerations

  • For Patent Holders:
    Ensure claims are sufficiently broad to prevent easy design-arounds while providing clarity and enforceability. Maintain robust documentation and consider extensions or supplementary protections, such as supplementary patent applications or formulations.

  • For Competitors:
    Conduct detailed freedom-to-operate analyses, scrutinizing overlapping claims and potential design-arounds. Consider alternative compounds or formulations outside the scope of AU366507.

  • For Market Participants:
    Understand patent expiration timelines to plan product launches. Monitor ongoing patent filings and oppositions that could influence the competitive landscape.


Conclusion

Australian Patent AU366507 exemplifies a crucial asset in the pharmaceutical patent landscape, primarily defined by its claims’ breadth and specificity. Its scope appears to encompass a novel chemical entity or therapeutic use, with potential overlaps in related patents shaping market and legal strategies. Stakeholders must analyze the claims diligently, considering prior art, patent family positioning, and market exclusivity, to navigate the complex Australian patent environment successfully.


Key Takeaways

  • Claim Precision Is Paramount: The scope hinges on the language used; broad claims enhance protection but risk validity challenges, while narrow claims limit enforceability.
  • Patent Landscape Is Complex: Overlapping patents in the same therapeutic space necessitate detailed freedom-to-operate assessments.
  • Strategic Patent Filing: Continued patent prosecution and international filings strengthen market position, especially prior to patent expiry.
  • Monitoring Legal Developments: Stay vigilant to legal challenges, oppositions, and EPO/Australian Patent Office guidelines impacting patent validity.
  • Market Entry Window: Exploit patent expiration dates and new patent filings to optimize commercialization strategies.

FAQs

1. What is the primary scope of AU366507?
It relates to a specific pharmaceutical compound or formulation, including its therapeutic use and manufacturing process, as defined by its claims.

2. How does AU366507 compare with similar patents internationally?
Its scope may overlap with patents filed in other jurisdictions; examining the patent family reveals similarities and differences, influencing global patent strategies.

3. Can competitors develop similar drugs outside the patent’s scope?
Yes, if their compounds or methods do not infringe on the specific claims or are sufficiently distinct, they may avoid infringement.

4. When does AU366507 expire, and what does that mean for market exclusivity?
Typically 20 years from the priority date, after which generic or alternative products can enter the market.

5. How important are the claims in enforcing the patent?
Extremely. The claims specify legal rights and boundaries; their clarity and breadth determine enforcement strength.


References

[1] Australian Patent Law Overview — Patent Act 1990 (Cth) and related provisions.
[2] Patent Claims Analysis — WIPO Patent Drafting Guidelines.
[3] Australian Patent Office Examination Guidelines — IP Australia.

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