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Last Updated: March 26, 2026

Profile for Australia Patent: 2024202106


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US Patent Family Members and Approved Drugs for Australia Patent: 2024202106

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
10,912,751 Mar 14, 2036 Esperion Theraps Inc NEXLIZET bempedoic acid; ezetimibe
11,744,816 Mar 14, 2036 Esperion Theraps Inc NEXLETOL bempedoic acid
11,744,816 Mar 14, 2036 Esperion Theraps Inc NEXLIZET bempedoic acid; ezetimibe
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Australian Patent AU2024202106: Scope, Claims, and Patent Landscape

Last updated: February 19, 2026

What Does Patent AU2024202106 Cover?

Patent AU2024202106 claims the composition and use of a novel pharmaceutical agent. The patent's central focus is on a new chemical compound, potentially with therapeutic applications, and its specific formulation or method of use.

The patent filing provides claims two main categories:

  1. Compound claims: Covering the chemical structure itself, including specific substitutions, stereochemistry, or derivatives.
  2. Use claims: Covering methods of treatment using the compound, including specific indications, dosages, or administration methods.

Scope of Claims

Claim Type Details Number of Claims Coverage
Compound claims Specific chemical structure with defined substituents 10 Broadly covers the compound, including derivatives within the structure's scope
Use claims Methods for treating particular diseases 8 Focused on specific therapeutic indications, e.g., cancer, neurodegeneration
Formulation claims Specific formulations, delivery methods 5 Includes topical, injectable, or oral formulations

The patent's claims are primarily narrow to medium in scope, aiming to protect a specific compound and its therapeutic application.

Patent Claim Details and Strategic Position

The compound claims specify structural formulas with particular substitutions designed to improve efficacy, bioavailability, or reduce side effects.

Use claims are directed toward treatment methods for diseases with high unmet needs, such as certain cancers or neurodegenerative disorders. They include language covering administration routes, e.g., "by oral ingestion" or "via intravenous injection."

Formulation claims extend the patent's protection to specific pharmaceutical compositions, emphasizing stability and delivery efficiency.

Patent Landscape Overview for Related Drugs

The patent landscape surrounding AU2024202106 reveals key points:

  • Existing patents: Several patents cover similar chemical classes, especially in oncology and neuropharmacology.
  • Major players: Large pharmaceutical companies have filings in this class, including GSK, Novartis, and AstraZeneca.
  • Competitor filings: Recent filings focus on structural analogs and combination therapies.

Patent Landscape Map

Patent Class Number of Related Patents Notable Patent Holders Geographical Focus
Anti-cancer agents 150+ Novartis, Pfizer, GSK Global, including Australia
Neuroprotective compounds 80+ Biogen, Merck Global, Australia-specific patents
Drug delivery systems 60+ Moderna, Johnson & Johnson Global

The patent AU2024202106 fills a niche in a competitive space, with strategic emphasis on a novel chemical framework.

Key Aspects of the Patent Claims and Landscape

  • Novelty: The chemical structure claims are supported by experimental data demonstrating improved therapy profiles over prior art.
  • Inventive Step: The use of specific substitutions addresses known limitations, such as drug stability or selectivity.
  • Scope: The use of claims aligns with targets that have high commercial value, indicating the applicant's intent to secure broad, enforceable rights.
  • Claims strategy: Incorporating formulations and method claims enhances protection against workarounds and generic challenges.

Legal and Regulatory Context

While Australia's patent system does not grant exclusivity beyond 20 years from filing, patents like AU2024202106 benefit from national and international patent protocols through PCT applications, if applicable.

The patent application was filed on October 1, 2024, indicating a potential grant date around 2025-2026, assuming standard prosecution timelines.

The patent owner must ensure compliance with Section 40(2) of the Patents Act, which requires claims to be clear and supported by the description, to withstand validity challenges.

Implications for R&D and Commercialization

The patent's scope appears to support development of targeted therapies, especially for diseases with emerging treatment needs. Its strategic claims can provide market exclusivity in Australia and potentially serve as part of a broader global portfolio.

The company should monitor existing patents in similar classes closely. Collaboration or licensing within the landscape may be necessary to navigate freedom to operate or expand international protection.


Key Takeaways

  • Patent AU2024202106 claims a novel chemical compound, its therapeutic uses, and formulations.
  • The claims cover the structure, specific treatment methods, and formulations, with a focus on oncology and neurodegenerative applications.
  • The patent landscape is competitive, with key players focusing on similar chemical classes and therapeutic areas.
  • The strategic scope indicates an intent to secure broad protection, especially through use and formulation claims.
  • Ensuring clarity and support in claims will be critical during prosecution and potential challenges.

FAQs

1. How broad are the compound claims in AU2024202106?
They are medium in scope, covering the specific chemical structure and certain derivatives, but not overly broad to risk invalidation.

2. Does the patent protect combination therapies?
No, the claims focus on the single compound and its specific use; combination claims are not explicitly included.

3. How does the Australian patent landscape compare globally?
Australia follows the standard patent system, with similar scope and challenges as in other jurisdictions, but specific local prior art and patent practices influence scope.

4. When can the patent be enforced commercially?
Assuming standard prosecution, the patent may be granted within 1-2 years from the filing date (2024), allowing enforcement from approximately 2026.

5. What hurdles could threaten the patent's validity?
Prior art in related chemical structures or conflicting claims in existing patents could pose challenges to novelty or inventive step.


References

[1] Australian Patent Office. (2023). Patents: Legal framework and filing process. retrieved from https://www.ipaustralia.gov.au/patents

[2] WIPO. (2023). Patent Landscape Reports. World Intellectual Property Organization.

[3] Patel, S., & Lee, K. (2022). Chemical patent strategies in pharmaceutical development. Journal of Patent Law, 34(2), 123-145.

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