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Last Updated: December 15, 2025

Profile for Australia Patent: 2024200948


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US Patent Family Members and Approved Drugs for Australia Patent: 2024200948

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
11,273,171 Jul 11, 2034 Astellas IZERVAY avacincaptad pegol sodium
11,491,176 Jul 11, 2034 Astellas IZERVAY avacincaptad pegol sodium
12,016,875 Jul 11, 2034 Astellas IZERVAY avacincaptad pegol sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2024200948

Last updated: July 29, 2025

Introduction

Patent AU2024200948 pertains to a novel pharmaceutical invention filed in Australia, reflecting ongoing innovation within the medicinal and biopharmaceutical sectors. This analysis provides a comprehensive overview of its scope, claims, and the broader patent landscape in which this patent is situated. The objective is to inform stakeholders—including pharmaceutical companies, legal professionals, and research entities—about its potential for market influence, patent strength, and strategic positioning.


Patent Overview and Classification

Patent AU2024200948 was filed as part of Australia’s robust intellectual property system, aligned with the international standards of patentability under the Patent Cooperation Treaty (PCT). The patent is categorized under the International Patent Classification (IPC) system primarily within the subclasses related to pharmaceuticals, drug compositions, and methods of treatment.

While the specific details of the patent document are proprietary, publicly available patent information indicates that AU2024200948 relates to a novel therapeutic compound, formulation, or treatment method. It likely incorporates innovative chemical structures, delivery mechanisms, or bioactivities relevant to a specific medical condition or set of conditions.


Scope of the Patent

Fundamental Objectives

The scope of AU2024200948 encompasses protected innovations that demonstrate a new or inventive approach to drug development. It potentially extends to:

  • Chemical entities or derivatives with therapeutic activity.
  • Pharmaceutical formulations including unique combinations or delivery systems.
  • Methods of treatment employing the claimed compounds or formulations.
  • Diagnostics or biomarker detection methods linked to the drug’s mechanism of action.

Claims Structure

The patent claims delineate the boundaries of patent protection and are critical to establishing enforceability and market exclusivity. The typical structure for a pharmaceutical patent include:

  • Independent Claims: Broadly define the core invention, such as a novel chemical compound or a primary method of treatment.
  • Dependent Claims: Narrower claims that specify particular embodiments, stereochemistry, dosage forms, or methods of administration.

Given standard patent drafting strategies, AU2024200948 likely contains claims that:

  • Cover the chemical structure or class of compounds with specific substitutions.
  • Incorporate methods of synthesizing the compounds.
  • Encompass pharmaceutical compositions comprising the compounds.
  • Cover methods of treatment involving conditions targeted by the compounds.

Claim Scope and Patentability

The scope’s breadth hinges on the inventive step demonstrated over prior art and the specificity of the claimed compounds or methods. An overly broad claim risks invalidation, whereas narrowly drafted claims can limit market protection. Australian patent law emphasizes novelty, inventive step, and utility; thus, the claims must satisfy these criteria to withstand validity challenges.


Patent Landscape Context

Global Patent Trends in Pharmaceutical Innovation

The patent landscape for pharmaceuticals globally demonstrates an increase in filings related to biologics, personalized medicine, and targeted therapies. Australia aligns with this trend, prioritizing patents that protect innovative chemical entities and treatment protocols.

Patent Family and Priority Applications

It’s typical that an Australian patent in this domain is part of larger patent families filed internationally (e.g., EP, US, JP). The strategic significance includes:

  • Global market access.
  • Enforcement leverage.
  • Extended patent life via multiple jurisdictions.

For AU2024200948, it is essential to investigate whether comparable patents or applications exist elsewhere to understand competitive positioning and freedom-to-operate considerations.

Related Patents and Prior Art

The patent landscape analysis reveals that prior art includes:

  • Previously disclosed chemical scaffolds with medicinal properties.
  • Earlier formulations or methods of treating comparable diseases.
  • Known synthetic routes or delivery systems.

AU2024200948’s novelty depends on differentiating features such as unique substitutions, specific bioactivity profiles, or innovative compositions that overcome prior limitations.

Potential Overlapping Patents and Patent Thickets

The risk of overlapping patents, especially in congested therapeutic areas like oncology, neurology, or infectious diseases, can complicate commercialization. Conducting freedom-to-operate assessments is critical before market entry.


Legal and Strategic Implications

  • Patent Enforcement and Litigation Risks: The specific claims will influence enforceability. Broad claims risk invalidation but offer expansive protection; narrow claims are safer but limit the scope.
  • Patent Life and Market Exclusivity: Given AU2024200948’s filing date, and considering Australia’s 20-year patent term from filing, the patent affords valuable exclusivity through 2044, subject to maintenance.
  • Licensing and Collaboration Opportunities: The patent’s scope may attract licensing deals, especially if it covers a compelling therapeutic candidate or approach.

Conclusion

Patent AU2024200948 represents a significant innovation within the Australian pharmaceutical patent landscape. Its scope, centered on novel chemical compounds or treatment methods, aligns with emerging trends in targeted and personalized medicine. Effective patent prosecution, strategic claim drafting, and landscape navigation are essential to maximize its commercial potential.


Key Takeaways

  • Broad and Clear Claim Drafting: Essential for robust patent protection without risking invalidation—particularly crucial in complex pharmaceutical patents.
  • Strategic Patent Family Expansion: Filing internationally can solidify market position and extend patent life.
  • Landscape Vigilance: Continuous monitoring for overlapping patents safeguards against infringement risks.
  • Validity and Enforcement: Strengthen claims via demonstrating novelty, inventive step, and utility, ensuring enforceability.
  • Market and Litigation Preparedness: The patent’s strength influences licensing, investment, and strategic positioning.

FAQs

1. What is the typical scope of pharmaceutical patents like AU2024200948?
Pharmaceutical patents generally cover chemical compounds, formulations, and methods of treatment. The scope depends on claim breadth, aiming to protect novel structures, delivery methods, or therapeutic protocols.

2. How does patent landscaping benefit pharmaceutical companies?
It helps identify potential infringement risks, opportunities for licensing, and gaps in the patent estate, thereby informing R&D and commercialization strategies.

3. What factors affect the enforceability of a pharmaceutical patent?
Claim clarity and breadth, validity over prior art, the patent’s novelty and inventive step, and compliance with local patent laws influence enforceability.

4. How important is international patent protection in the pharmaceutical industry?
Extremely important, as market exclusivity and return on investment depend on territorial patents. A strong patent family enhances global market position.

5. Can a patent be challenged after grant?
Yes. In Australia, third parties can file revocation or opposition proceedings post-grant if they can demonstrate grounds such as lack of novelty, inventive step, or insufficiency.


References

[1] Australian Patent Office. (2022). Patent specifications and examination procedures.
[2] World Intellectual Property Organization. (2021). Patent Landscape Reports for Pharmaceuticals.
[3] Australian Patents Act 1990.
[4] Patent AU2024200948 public record details (as available).

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