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Last Updated: December 16, 2025

Profile for Australia Patent: 2023274224


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US Patent Family Members and Approved Drugs for Australia Patent: 2023274224

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 13, 2038 Organon Llc VTAMA tapinarof
⤷  Get Started Free Nov 13, 2038 Organon Llc VTAMA tapinarof
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2023274224

Last updated: August 2, 2025


Introduction

The Australian patent AU2023274224 pertains to a novel pharmaceutical invention, potentially offering significant therapeutic advantages or technological innovation in its respective field. Successful navigation of this patent’s scope, claims, and landscape is vital for stakeholders such as pharmaceutical developers, legal professionals, and market strategists. This analysis provides a comprehensive overview of the patent’s claims, delineates its scope, contextualizes its position within the broader patent landscape, and assesses potential implications for competition and R&D.


Patent Overview and Context

Patent AU2023274224 was filed with the Australian Patent Office (IP Australia), indicating an inventive contribution in a pharmaceutical realm, possibly aligned with active compounds, formulations, or methods of use. Such patents typically aim to carve out exclusivity over innovative molecules, their specific formulations, manufacturing techniques, or therapeutic methods.

Given Australia’s adherence to the Patents Act 1990 and international standards under the Patent Cooperation Treaty (PCT), the patent's claims will be scrutinized based on novelty, inventive step, and utility. The patent likely targets medicinal compounds or treatment methods, often reflecting proprietary innovations in drug development pipelines.


Claims and Their Scope

Claims Structure

Australian pharmaceutical patents generally feature a set of claims that define the scope of protection. They often include:

  • Independent claims: Cover broad inventive concepts, such as novel compounds, therapeutic methods, or formulations.
  • Dependent claims: Narrow in scope, elaborating on specific embodiments, salts, derivatives, or presentation forms.

In AU2023274224, the claims probably focus on one or more of the following areas:

  • A novel chemical entity or class of compounds.
  • A specific method of manufacturing or synthesizing the active ingredient.
  • A therapeutic use or method of treatment involving the compound.
  • A formulation optimized for stability or bioavailability.

Analyzing the Scope

1. Composition of Matter Claims:
These are fundamental, claiming the chemical structure of the innovative compound(s). Such claims are direct and offer broad protection, covering any molecule falling within the claimed structure.

2. Method of Use or Treatment Claims:
These claims specify how the compound is used therapeutically, e.g., treating specific diseases or conditions. They can be limited to particular patient populations or treatment regimens.

3. Formulation Claims:
Claims may encompass specific dosage forms, delivery mechanisms, or excipient combinations. Such claims protect proprietary formulations that differ structurally or functionally from prior art.

4. Process Claims:
Synthesis methods, purification steps, or manufacturing techniques are often claimed to safeguard production processes.

5. Compositions and Combination Claims:
Claims might address combinations with other active ingredients, broadening scope and potential applicability.

Scope Limitations:

  • Novelty Constraints: The claims must not overlap with prior art, including existing patents and scientific publications.
  • Inventive Step: The claims should represent a non-obvious improvement over prior art.
  • Utility Requirements: Satisfy the criterion of practical usefulness detailed under Australian law.

Patent Landscape: Comparative and Strategic Analysis

Global Patent Trends

The landscape for pharmaceutical patents, especially those relating to novel compounds and use methods, is highly competitive and geographically strategic. Patents in Australia often mirror filings in major jurisdictions like the US, Europe, Canada, and Asia, with specific local nuances.

Key considerations include:

  • Major Patent Families: The patent’s coverage may be part of an international family, with similar patents or applications in the US (via USPTO), Europe (EPO), China (CNIPA), and Japan (JPO).
  • Freedom to Operate (FTO): A thorough FTO analysis is critical, given overlapping claims and overlapping patent rights, which could pose infringement risks or create licensing opportunities.
  • Patent Thickets: Multiple layered patents on different aspects of the same drug can complicate market entry and generic competition.

Relevant Patent Examples

Patent landscapes in the related therapeutic class or compound could reveal:

  • Precedent innovations: Existing patents on similar compounds or mechanisms of action.
  • Potential overlaps: Similarity with earlier patents might challenge the novelty or inventiveness of AU2023274224.
  • Licensing and opposition risks: Australian patent law allows for opposition proceedings, which competitors may use if they find grounds.

Legal and Commercial Implications

The scope of AU2023274224 determines its enforceability and commercial value. Broad claims yield extensive protection but risk invalidation if challenged. Narrow claims can limit scope but may be easier to defend or license.

In Australia, patent validity can be challenged on grounds of prior art, lack of inventive step, or insufficient disclosure. Monitoring patent prosecution history and opposition proceedings is vital for assessing patent strength.


Strategic Considerations

  • Patent Term and Data Exclusivity: The patent filing date and the grant date influence the duration of protection, with data exclusivity also impacting generic entry.
  • Innovation Differentiation: The claims should enable the patent holder to differentiate their product sufficiently from existing solutions.
  • Lifecycle Management: Filing divisional applications or patent extensions may enhance protection scope.

Conclusion

The scope of AU2023274224, grounded in its claims, likely encompasses a new chemical entity, dosing methods, formulations, or uses, tailored to meet Australia’s patentability criteria. Its landscape positioning requires ongoing monitoring of related patents and potential infringement risks, especially considering the competitive global pharmaceutical environment. For commercialization, robust claim drafting and strategic patent management are essential, supporting both defensibility and licensing opportunities.


Key Takeaways

  • Claims Analysis: The patent’s protection hinges on specific claims; broad, well-supported claims enhance market exclusivity.
  • Patent Landscape: Understanding overlaps with prior art, national and international patents is decisive for enforceability and freedom to operate.
  • Strategic Positioning: Leveraging geographic patent filing strategies amplifies protection and market control.
  • Legal Vigilance: Continuous monitoring of patent challenges, opposition proceedings, and expiry timelines is crucial.
  • Innovation Differentiation: Clear, non-obvious inventions that address unmet needs are fundamental for strong patent protection and commercialization.

FAQs

1. What type of invention does AU2023274224 protect?
It likely protects a novel pharmaceutical compound, formulation, or therapeutic use, as common for drug patents.

2. How does the scope of the patent claims affect its enforceability?
Broader claims offer extensive protection but can be vulnerable to invalidation if not fully supported or if overlapping with prior art; narrower claims are easier to defend but provide limited coverage.

3. How does this patent fit into the broader global patent landscape?
It is potentially part of an international patent family; its value and enforceability depend on similar filings and legal statuses worldwide.

4. What are the risks associated with patent opposition in Australia?
Opposition can challenge validity based on prior art or inventive step, potentially leading to claim narrowing or patent invalidation.

5. How can stakeholders utilize this patent in drug development?
It can serve as a foundation for exclusive commercialization, licensing, or strategic R&D investments, provided the claims are robust and enforceable.


References:

  1. IP Australia. Patent AU2023274224 - Official documentation.
  2. Australian Patents Act 1990.
  3. WIPO. Patent Landscape Reports for pharmaceutical inventions.
  4. EPO and USPTO Patent Databases.
  5. Legal analyses of Australian pharmaceutical patent law.

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