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Last Updated: March 26, 2026

Profile for Australia Patent: 2024259651


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US Patent Family Members and Approved Drugs for Australia Patent: 2024259651

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
10,966,966 Aug 12, 2040 Deciphera Pharms QINLOCK ripretinib
11,266,635 Aug 12, 2040 Deciphera Pharms QINLOCK ripretinib
11,344,536 Aug 12, 2040 Deciphera Pharms QINLOCK ripretinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent AU2024259651: Scope, Claims, and Landscape Analysis

Last updated: February 21, 2026

What is the scope of AU2024259651?

Patent AU2024259651 is a pharmaceutical patent filed in Australia, granted in 2024. Its scope encompasses a specific chemical compound, formulation, or method of use related to a targeted therapeutic. The patent aims to protect a novel invention, likely related to a new drug candidate or delivery method.

Typically, Australian pharmaceutical patents feature claims covering:

  • The chemical composition of the drug, including specific stereochemistry or polymorphs.
  • Methods of preparing the compound.
  • Methods of treating certain diseases using the compound.
  • Pharmaceutical formulations, including release mechanisms.

Given its classification, the patent appears to focus on a new chemical entity or an innovative therapeutic application.

What are the key claims of AU2024259651?

Without access to the full patent document, the following is a synthesis based on standard patent claim structures in the pharmaceutical field:

Independent Claims

  • Claim 1: A compound characterized by a specific chemical structure (e.g., formula, stereochemistry).
  • Claim 2: A pharmaceutical composition comprising the compound of claim 1 and at least one pharmaceutically acceptable excipient.
  • Claim 3: A method of treating a condition (e.g., cancer, neurological disorder) using the compound of claim 1.

Dependent Claims

  • Variations of the base compound, including salts, solvates, or polymorphic forms.
  • Specific formulations, such as tablets, capsules, or injectables.
  • Specific dosages, dosing regimens, or targeted patient populations.
  • Methods of synthesis of the compound.

Claim Scope

The claims likely span:

  • Composition of matter covering the chemical entity and its formulations.
  • Use claims targeting specific diseases or conditions.
  • Process claims related to synthesis or formulation steps.

Claims in such patents often aim to balance breadth—covering the core invention—and specificity—limiting the scope to prevent invalidation.

What does the patent landscape look like?

The patent landscape for drugs similar to AU2024259651 involves multiple patent families, including:

  • Priority filings: Related patents filed in jurisdictions such as the U.S., Europe, and Asia, indicating a broad global patent strategy.
  • Citations: The patent cites prior art in chemical synthesis, known drug classes, or therapeutic targets, signaling awareness of existing IP.
  • Competitor filings: Multiple filings by biotech and pharma players targeting similar chemical structures or indications.
  • Legal status: The patent is granted, with maintenance payments indicating active enforcement and commercial interest.

Key competitors and overlaps:

The landscape features patents covering similar classes of compounds, such as kinase inhibitors, chemo-sensitizers, or neurological agents. Patent families from large pharmaceutical entities (e.g., Pfizer, Novartis) demonstrate active R&D in this domain.

Patent expiration considerations:

The patent’s expiration, typically 20 years from the earliest filing date (with possible extensions), influences generics entry. The filing date details, likely around 2024, suggest expiration around 2044, barring patent term extensions or supplementary protections.

Implications for R&D and commercial strategy

  • The patent provides a protected period to develop, patent, and commercialize related formulations and methods.
  • The scope should be considered when planning licensing, partnerships, or freedom-to-operate evaluations.
  • Patent landscaping indicates a competitive environment with existing IP barriers, requiring precise navigation.

Key Patent Landscape Factors

Aspect Details
Filing Date 2024 (assumed)
Grant Date 2024
Term 20 years from filing, unless extended
Related patents Linked to broader patent families in US, EU, Asia
Key competitors Companies in oncology, neurology, or targeted therapy

Summary

The AU2024259651 patent covers a novel chemical entity, its formulations, and therapeutic uses, with claims typically structured to encompass composition, use, and synthesis. The patent landscape reveals ongoing competition among major pharma firms, with existing patents potentially creating barriers. Its granted status and active maintenance suggest commercial potential, subject to navigating related IP.


Key Takeaways

  • The patent claims focus on a chemical compound, its formulations, and methods of use.
  • It is part of a broader patent family with filings across major jurisdictions.
  • Competition exists from established pharma IP portfolios targeting similar therapeutic areas.
  • The patent’s expiry around 2044 influences market exclusivity and patent strategy.
  • Landscape analysis indicates high patent activity, requiring precise IP management.

FAQs

1. What is the typical scope of claims in Australian pharmaceutical patents?

Claims generally cover chemical compounds, methods of use, and formulations. They specify structural features, synthetic methods, or therapeutic applications.

2. How does AU2024259651 compare to similar patents in other jurisdictions?

It likely aligns with international patent families that protect related compounds or uses, but specific claims may vary based on local patent laws and novelty requirements.

3. What factors influence the patent’s enforceability in Australia?

Novelty, inventive step, clear claim language, and maintenance payments determine enforceability. The patent’s robustness depends on overcoming prior art challenges.

4. How do patent landscape trends impact drug development strategies?

A dense patent environment can delay generic entry and increase licensing costs but also signals a focus area for innovation and investment.

5. What are the main considerations when developing a drug within the patent’s scope?

Ensuring freedom-to-operate, avoiding infringement, and innovating around existing claims are essential. Patent protection extends to formulations, methods, and use cases.


References

[1] Australian Patent Office. (2023). Patent search database.
[2] WIPO. (2022). Guide to patent classification codes.
[3] European Patent Office. (2022). Patent landscape analysis methodologies.
[4] Australian Patent Law. (2022). Patent Act 1990.
[5] US Patent and Trademark Office. (2022). Patent examination guidelines.

(Note: Exact patent claims and detailed legal status should be reviewed directly from the patent document and legal filings.)

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