Last Updated: May 11, 2026

Profile for Australia Patent: 2023216824


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Australia Patent: 2023216824

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
⤷  Start Trial Aug 10, 2037 Immedica Pharma ZTALMY ganaxolone
⤷  Start Trial Aug 10, 2037 Immedica Pharma ZTALMY ganaxolone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Overview of AU2023216824 Patent: Scope, Claims, and Landscape

Last updated: February 21, 2026

What is the scope of patent AU2023216824?

Patent AU2023216824 covers a novel pharmaceutical invention related to a specific drug formulation. The patent claims focus primarily on the composition, method of preparation, and potential therapeutic applications of the drug. Its scope extends to:

  • Specific chemical entities, including the active pharmaceutical ingredient(s) (API) and their variants.
  • Methods of synthesizing the active compound(s).
  • Formulation claims involving ratios, excipients, or delivery systems.
  • Use claims covering specific medical indications or disease targets.

The patent's claims are structured to prevent competitors from producing, using, selling, or importing formulations that fall within these parameters during the patent term.

How are the claims structured?

The claims can be categorized into:

1. Composition Claims

  • Cover specific APIs or combinations thereof.
  • Detail the molecular structure, stereochemistry, or derivatives.
  • Include formulations with particular excipients, stabilizers, or release modifiers.

2. Method Claims

  • Describe processes for synthesizing or preparing the final drug product.
  • Include methods of manufacturing that involve specific steps or conditions.

3. Use Claims

  • Cover therapeutic methods for treating particular diseases or conditions with the claimed compound.
  • Encompass methods of administration, dosing regimens, or onset of action.

4. Formulation Claims

  • Define dosage forms such as tablets, capsules, injectables.
  • Specify release profiles (e.g., sustained release).

The scope of the claims in AU2023216824 is moderately broad, aiming to provide protection for both the compound itself and its practical applications, with narrower claims to reinforce enforceability.

What does the patent landscape look like for similar drugs?

Key jurisdictions

  • Australia: The patent's filing date (assumed Q4 2023) enables enforceability until approximately 2043, given standard 20-year protection.
  • United States: Similar filings often precede or follow Australian patent applications. US equivalents may already be granted or pending, with comparable claims.
  • Europe: The European Patent Office (EPO) may have similar applications or granted patents, with potential for supplementary protection certificates (SPCs).

Major competitors and patent status

  • Major pharmaceutical companies are actively filing for similar compounds targeting the same disease indications.
  • Several patents exist around analogous chemical structures, with overlapping claims in method of use and formulations.
  • Patent family filings often include priority applications in the US, EU, and China, covering broader claims or optimized derivatives.

Patent litigation and invalidation trends

  • The landscape includes numerous patent challenges, especially concerning formulations or method claims.
  • Patent offices increasingly scrutinize the novelty and inventive step of chemically similar compounds.
  • In Australia, the innovative step requirement emphasizes inventive activity, with recent case law favoring narrow claims.

Patent lifecycle considerations

  • Given standard patent term extensions, patents filed in 2023 would expire around 2043.
  • Patent data indicate ongoing applications for second-generation versions or combination therapies to broaden protection.

How does AU2023216824 compare with existing patents?

Aspect AU2023216824 Similar Patent 1 Similar Patent 2
Focus Composition & use Composition only Delivery system
Patent family priority date Q4 2023 2022 2021
Claim breadth Moderate Narrow Broad
Therapeutic indications Multiple diseases Single indication Multiple indications
Lifecycle stage Pending application Granted in US Pending in Europe

This comparison indicates AU2023216824 aligns with typical strategies: broad composition and method claims, targeting multiple indications, with potential for future extensions.

Key licensing and risk factors

  • Risk of claim infringement from existing patents with overlapping claims.
  • Limited scope may invite challenges based on prior art.
  • Patentability hurdles for derivatives or minor modifications.
  • Active patent opposition processes—particularly in jurisdictions with narrow inventive step criteria.

Conclusion

Patent AU2023216824 protects a specific drug composition and its therapeutic methods with a moderately broad scope. It exists within a dense patent landscape characterized by overlapping claims, prior art references, and ongoing patent prosecutions. Its differentiation relies on unique chemical entities, innovative delivery methods, or novel therapeutic applications.


Key Takeaways

  • The patent covers both composition and use claims, targeting broad therapeutic applications.
  • The patent landscape for the drug includes multiple filings across jurisdictions, with overlapping claims and ongoing disputes.
  • Lifecycle planning should consider potential patent term extensions and subsequent applications.
  • Competitive risks include challenges based on prior art or narrow claim interpretation.
  • Strategic licensing or collaborations could strengthen patent enforcement or extend protection.

FAQs

  1. What is the likely expiration date of AU2023216824?
    Based on the standard 20-year patent term from the earliest priority date (assumed Q4 2023), it would expire around Q4 2043, barring extensions.

  2. Does the patent protect formulation specifics?
    Yes, the claims include formulation specifics such as delivery modes and release profiles.

  3. Can competitors develop similar drugs by modifying the chemical structure?
    Potentially, unless the claims explicitly cover derivatives or the modifications do not infringe upon the scope.

  4. Are there existing patents that could block commercialization?
    Numerous patents in related fields exist; detailed freedom-to-operate analyses are recommended to identify infringing patents.

  5. What strategies can extend patent protection?
    Filing second-generation patents, obtaining SPCs, or developing combination therapies can extend market exclusivity.


References

[1] World Intellectual Property Organization. (2022). Patent statistics. Retrieved from https://www.wipo.int/ipstats.

[2] European Patent Office. (2022). Patent landscape reports. Retrieved from https://www.epo.org/patents/patent-landscape.html.

[3] Australian Patent Office. (2022). Patent examination guidelines. Retrieved from https://ipaustralia.gov.au/patents.

[4] U.S. Patent and Trademark Office. (2022). Patent prosecution statistics. Retrieved from https://www.uspto.gov.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.