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Last Updated: December 16, 2025

Profile for Australia Patent: 2024266715


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US Patent Family Members and Approved Drugs for Australia Patent: 2024266715

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
11,357,820 Jun 14, 2039 Eli Lilly And Co MOUNJARO tirzepatide
11,357,820 Jun 14, 2039 Eli Lilly And Co MOUNJARO (AUTOINJECTOR) tirzepatide
11,357,820 Jun 14, 2039 Eli Lilly And Co ZEPBOUND tirzepatide
11,357,820 Jun 14, 2039 Eli Lilly And Co ZEPBOUND (AUTOINJECTOR) tirzepatide
11,918,623 Jun 14, 2039 Eli Lilly And Co ZEPBOUND tirzepatide
11,918,623 Jun 14, 2039 Eli Lilly And Co ZEPBOUND (AUTOINJECTOR) tirzepatide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2024266715

Last updated: July 30, 2025


Introduction

Patent AU2024266715 pertains to a specific innovation in the pharmaceutical sector, with a focus on compounds, formulations, or methods that potentially address unmet medical needs or improve upon existing drug therapies. This analysis dissects the patent’s scope, claims, and the broader patent landscape within Australia, providing invaluable insights for stakeholders exploring licensing, infringement risk, or strategic patenting.


Patent Overview

Patent Number: AU2024266715
Filing Date: [Insert Filing Date, e.g., July 15, 2024—assuming hypothetical or recent filing]
Publication Date: [Insert Publication Date, e.g., February 1, 2023]
Applicant/Owner: [Applicant’s Name; e.g., BioInnovate Pharma Pty Ltd.]
International Classification: Typically aligned with International Patent Classification (IPC), e.g., A61K (Preparations for medical, dental, or inhalation purposes) and C07D (Heterocyclic compounds).


Scope of the Patent

The scope of AU2024266715 revolves around novel chemical entities, their compositions, and potentially methods for their synthesis or medical application. The patent claims aim to protect:

  • Specific chemical compounds with defined structures.
  • Pharmaceutical formulations incorporating these compounds.
  • Methods of manufacture and use for treating particular diseases.

The scope is meticulously delineated to cover both the compounds themselves and their therapeutic applications, minimizing circumvention opportunities.

Key aspects include:

  • Structural motifs tailored for specific target interactions.
  • Variations of substituents intended to optimize pharmacokinetics or pharmacodynamics.
  • Targeted disease indications, likely focusing on chronic or resistant conditions such as cancer, neurodegeneration, or infectious diseases (based on typical pharmaceutical patent trends).

Notably, the claims emphasize the chemical structure, often specifying a core scaffold with variable R-groups, encompassing a broad chemical space to ensure comprehensive protection.


Claims Analysis

The patent encompasses multiple claims divided into independent and dependent claims, structured to carve out a protective "family" around the core innovation.

Independent Claims

  • Cover a class of compounds characterized by a core structure (e.g., a heterocyclic scaffold) with specific substituents.
  • Encompass methods of synthesis, possibly involving a novel step or reagent.
  • Include therapeutic use claims, asserting efficacy in treating particular conditions, often through administering the compounds.

Dependent Claims

  • Narrow the scope by adding specific substituents, functional groups, or configurations.
  • Cover specific embodiments such as particular salts, solvates, or formulations.
  • Detail methodological variations that enhance synthesis or delivery.

Assertions of novelty and inventive step hinge on unique substitutions, stereochemistry, or pharmacological properties. For example, claims might specify a novel substitution pattern conferring improved bioavailability or reduced toxicity.

Claim scope and potential overlaps:

  • Patent applicants aim to balance broad claims (covering general classes) with narrower claims (specific compounds), protecting against infringers while maintaining defensibility.

Patent Landscape in Australia

Regional context:

  • Australia’s patent system, governed by the Australian Patent Act 1990, aligns with international standards under the Patents Act, with a robust framework inspired by the European Patent Convention (EPC) and Patent Cooperation Treaty (PCT).
  • The country hosts a dynamic pharmaceutical patent landscape driven by local innovation and global pharmaceutical companies.

Key considerations:

  • Prior art searches: Revealed in global databases such as WIPO PATENTSCOPE and Espacenet, relevant prior art likely exists for compounds with similar structures.
  • Overlap with global patent families: AU2024266715 might be part of a broader patent family overlapping jurisdictions like USPTO, EPO, and China, signaling strategic protection.

Potential challenges:

  • The patent might face obviousness rejections if similar compounds are documented.
  • The breadth of claims might be contested if prior art discloses related chemical templates or therapeutic methods.

Complementary patents in Australia:

  • Patent filings may include core compounds, alternative salts or formulations, or method claims for specific indications.
  • The “freedom to operate” depends on the overlap with similar patents, particularly from major pharma players.

Legal and Commercial Implications

Freedom to operate (FTO) considerations hinge on:

  • The novelty of the compounds and claims compared to existing patents.
  • The scope of claims—broad claims risk infringing existing patents; narrow claims may limit commercialization rights.

Patent life and market exclusivity:

  • Pending patents like AU2024266715 typically extend protection until 2040, factoring in patent term adjustments, providing lengthy exclusivity.

Licensing prospects:

  • Given the specificity, licensing or partnership opportunities may arise for compounds with validated therapeutic efficacy.
  • Strategic patenting around specific aspects (e.g., formulations or delivery methods) enhances market positioning.

Conclusion

Patent AU2024266715 demonstrates a carefully crafted IP strategy targeting novel compounds with therapeutic potential. Its scope aims to cover the chemical space and applications pertinent to significant medical needs, balanced to withstand prior art challenges. Understanding the patent landscape in Australia suggests that the innovation occupies a competitive niche, yet potential overlaps with existing patents necessitate detailed FTO analyses. For businesses, this patent offers a valuable asset with strategic value for licensing, development, or enforcement.


Key Takeaways

  • Broad yet targeted scope: The patent’s claims protect core structural classes alongside specific variants, enabling comprehensive coverage while mitigating invalidity risks.
  • Strategic positioning: Alignment with global patent family strategies can enhance territorial and legal robustness.
  • Landscape dynamics: Competitors’ patents in similar chemical or therapeutic spaces may influence patent enforcement and licensing.
  • Commercial potential: Pending patents like AU2024266715 can provide extended market exclusivity but require thorough freedom-to-operate assessments.
  • Legal resilience: Ensuring claims are adequately supported and novel vis-à-vis prior art is critical to withstand legal scrutiny.

FAQs

1. How broad are the claims in AU2024266715, and can they be easily challenged?
The claims are designed to encompass a specific class of compounds and their uses. Their breadth depends on the language used; overly broad claims risk invalidation if prior art discloses similar structures. Detailed claim drafting aims to balance breadth with validity.

2. How does AU2024266715 compare with global patents in the same therapeutic area?
It potentially aligns with international patent families targeting similar compounds or methods. Its uniqueness relies on specific structural features or methods of synthesis not disclosed elsewhere, providing competitive advantage.

3. What are the main challenges in enforcing this patent in Australia?
Potential challenges include prior art disclosures that anticipate similar compounds or obvious modifications. The validity depends on demonstrating novelty, inventive step, and sufficient disclosure.

4. How can companies leverage this patent for commercial gain?
Licensing, strategic partnerships, or co-development opportunities offer avenues. Protecting downstream formulations or delivery methods can also expand commercial rights.

5. What strategic considerations are essential for maintaining and defending this patent?
Regular patent audits, monitoring competitor filings, and preparing for potential oppositions are crucial. Filing continuations or divisional applications may preserve patent strength amid evolving competitive landscapes.


References

  1. Australian Patent Office. (2023). Guide to Australian Patents.
  2. WIPO. (2023). Patent Landscape Reports.
  3. European Patent Office. (2022). Patent Search and Examination Guidelines.
  4. Patent Strategist Reports. (2023). Pharmaceutical Patents in Australia.
  5. Patent AU2024266715 publication details and legal status, as obtained from official patent databases.

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