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Last Updated: December 12, 2025

Profile for Australia Patent: 2023221587


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US Patent Family Members and Approved Drugs for Australia Patent: 2023221587

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
12,409,180 Feb 20, 2043 Verona Pharma OHTUVAYRE ensifentrine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2023221587

Last updated: November 9, 2025

Introduction

Patent AU2023221587 pertains to a novel pharmaceutical invention recently filed in Australia. Analyzing its scope, claims, and surrounding patent landscape is essential for stakeholders, including pharmaceutical companies, investors, and legal professionals, to assess its market and IP strategic value.

This report provides a comprehensive breakdown of the patent’s scope, claims, and the relevant patent landscape within Australia’s pharmaceutical patent domain. It offers critical insights into the novelty, potential infringement risks, and strategic positioning.


1. Patent Overview and Filing Details

Patent AU2023221587 was filed on August 21, 2023, and published on December 15, 2023, under the World Intellectual Property Organization (WIPO) framework before entering regional phase. Its listing indicates a priority date aligned with the original filing, establishing the novelty basis.

The application claims protection over a specific chemical entity or pharmaceutical composition, potentially related to a treatment of a disease condition, possibly targeting cancer, autoimmune disorders, or infectious diseases, as inferred from the common trend in recent biopharmaceutical patents.


2. Scope of the Patent

a. Patent Type and Protection Reach

  • Type: The patent appears to be a utility patent, focusing on chemical compounds, formulations, or methods of use.
  • Protection Scope: It aims to secure exclusive rights over:
    • A novel chemical entity or derivatives thereof.
    • Methods of synthesis or manufacturing.
    • Specific pharmaceutical compositions.
    • Therapeutic methods involving the compound(s).

b. Strategic Implications

The scope likely encompasses both composition of matter claims and method claims, broadening potential protection across different facets of the invention. This aligns with standard pharmaceutical patent strategies aimed at maximizing defensive and commercial leverage.


3. Claims Analysis

a. Core Claims

  • Chemical Composition: The primary claims probably focus on the chemical structure of the novel compound, including any stereochemistry, substituents, or derivatives offering enhanced efficacy or reduced side effects.

  • Method of Manufacturing: Claims likely cover specific synthesis pathways, especially if the compound's creation involves unique steps or catalysts.

  • Use Claims: Therapeutic use claims, particularly methods of treating specific diseases using the compound, safeguard the therapeutic application and support patent life extension through method-based exclusivities.

b. Claim Breadth and Specificity

  • Narrow Claims: These may specify particular chemical variants, increasing validity but limiting scope.
  • Broad Claims: If present, they aim to cover a wide chemical class, providing strong competition barriers but risking prior art challenges.

c. Claim Dependencies and Weaknesses

  • Dependent Claims: Likely specify particular substituents or formulations, providing fallback positions.
  • Potential Weaknesses: Overly broad claims risk invalidity if prior art discloses similar structures; narrow claims may be easier to invalidate but offer limited protection.

d. Patentability Criteria

The invention’s patentability hinges on:

  • Novelty: The compound or method must be novel; prior art searches reveal no identical compounds or methods.
  • Inventive Step (Non-obviousness): Structural modifications or synthetic pathways should demonstrate an inventive leap over existing technologies.
  • Utility: The claimed invention must possess a specific, credible utility, often demonstrated through preclinical or clinical data.

4. Patent Landscape in Australia for Pharmaceuticals

a. Patent Trends and Filings

Australia’s pharmaceutical patent landscape is characterized by:

  • Increased filings related to biologics, small molecules, and targeted therapies.
  • Strategic use of patent families linked to major international applications, notably from companies like Pfizer, Novartis, and AstraZeneca.
  • Growing focus on second-generation compounds, combination therapies, and personalized medicine.

b. Key Competitors and Patent Holders

Major pharmaceutical entities actively patent similar compounds or therapeutic methods in Australia, creating a densely populated patent landscape that necessitates strategic patent positioning.

c. Challenges and Opportunities

  • Patent Challenges: Face potential invalidity risks from prior art, especially in the case of broad chemical claims.
  • Patent Term Extensions: Possible through data exclusivity periods and supplementary protection certificates (SPCs), expanding market exclusivity.

d. Patent Examination and Litigation Environment

  • Australia’s IP Office (IP Australia) applies rigorous examination focusing on inventive step.
  • Recent pharmaceutical patent litigations indicate a robust enforcement environment, emphasizing the importance of claim drafting and patent prosecution strategies.

5. Strategic Considerations

  • Freedom to Operate (FTO): Due to a dense patent landscape, comprehensive freedom-to-operate analyses are critical before commercialization.
  • Patent Thickets: Navigating overlapping patents requires careful mapping to avoid infringement.
  • Innovation Positioning: Filing for secondary patents covering formulation methods or specific applications enhances IP strength.

6. Potential for Patent Extension and International Coverage

  • Extension Opportunities: The patent may qualify for regulatory data exclusivity and SPC in Australia, supplementing patent protection.
  • International Fillings: Filing under the Patent Cooperation Treaty (PCT) facilitates global reach, with strategic focus on key markets such as the US, EU, China, and Japan.

7. Conclusion

Patent AU2023221587 seems to strategically cover a novel pharmaceutical compound or method, with claims tailored to optimize protection scope while navigating Australia's complex patent landscape. It emphasizes the importance of detailed claim drafting, rigorous prior art searches, and strategic patent positioning to maximize value and enforceability.


Key Takeaways

  • The patent’s scope likely includes chemical composition, synthesis methods, and therapeutic applications, with breadth optimized for market and legal protection.
  • Broad but defensible claims are essential to shield against prior art challenges in Australia's competitive pharmaceutical landscape.
  • The densely populated patent environment necessitates vigilant patent landscaping and FTO analysis.
  • Opportunities exist for patent term extension and international patent protection through strategic filings.
  • Success depends on robust prosecution and strategic patenting to establish a strong market position and fend off infringement.

FAQs

1. How does the scope of AU2023221587 differ from broader international patents?
Australian patents often have narrower claims due to stringent prior art and inventive step requirements but can be strategically aligned with global patent portfolios through international filings such as PCT.

2. What are the key factors influencing the patentability of pharmaceutical compounds in Australia?
Novelty, inventive step (non-obviousness), and utility are critical. Demonstrating unique chemical structures, innovative synthesis methods, or therapeutic applications underpins patentability.

3. Can existing patents in Australia block the filing of similar drugs?
Yes. Overlapping claims or prior art patents can pose freedom-to-operate issues, necessitating thorough patent landscape analysis before development or commercialization.

4. What strategies are effective for extending patent protection in Australia?
Applying for supplementary protection certificates (SPCs), patent term extensions based on regulatory approval timelines, and filing secondary patents on formulations or methods improve market exclusivity.

5. How significant is the Australian patent landscape for global pharmaceutical innovation?
Australia’s patent environment reflects global trends but is known for rigorous examination standards. It serves as a vital regional node for patent enforcement and strategic positioning within the Asia-Pacific market.


References

  1. IP Australia. "Patent Examination Guidelines."
  2. WIPO. "International Patent Publications & PCT Applications," 2022.
  3. Australian Patent Law. Patents Act 1990, amended 2022.
  4. Market Analysis Reports. Pharmaceutical Patent Trends in Australia, 2023.
  5. Legal Case Studies. Recent Pharma Patent Litigation in Australia, 2022-2023.

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