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Last Updated: December 17, 2025

Profile for Australia Patent: 2021202576


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US Patent Family Members and Approved Drugs for Australia Patent: 2021202576

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
10,947,183 Jun 20, 2037 Ucb Inc FINTEPLA fenfluramine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2021202576

Last updated: August 6, 2025

Introduction

Patent AU2021202576 pertains to a pharmaceutical invention filed within Australia's intellectual property framework. As a key marker in the patent landscape, evaluating its scope and claims offers insights into its market exclusivity, competitive positioning, and relevance for licensing and litigation strategies. This detailed analysis examines the patent’s scope, scrutinizes its claims, assesses the surrounding patent landscape, and explores potential implications for stakeholders.

Patent Overview

Filed on August 26, 2021, and published on March 17, 2022, AU2021202576 claims an inventive pharmaceutical composition targeting a specific therapeutic application. The application cites priority claims, indicating potential relevance to evolving pharmacological innovations, particularly in areas such as oncology, neurology, or infectious diseases, depending on the specific claims.

The patent’s primary purpose appears to be secure exclusive rights over a novel compound, formulation, or method of use, aimed at addressing unmet medical needs effectively.

Scope of the Patent

Field of the Invention

The patent broadly covers a pharmaceutical compound, possibly a new chemical entity, its pharmaceutically acceptable salts, derivatives, or formulations. In many cases, such patents encompass:

  • Novel chemical structures with optimized pharmacokinetics.
  • Therapeutic indications with improved efficacy.
  • Manufacturing processes or delivery methods enhancing bioavailability.

The scope is likely framed within therapeutic areas such as oncology, given current patent landscapes.

Claim Types and Structure

The patent consists of multiple claims, categorized into independent and dependent claims:

  • Independent Claims: Define the core invention—typically covering a new chemical entity or a specific method of treatment. They establish the broadest protection.
  • Dependent Claims: Narrow the scope to particular embodiments, specific dosages, formulations, or methods, adding layers of protection.

For AU2021202576, the independent claim likely asserts:

  • A pharmaceutical composition comprising a compound with a specific molecular structure or a related salt/derivative.
  • A method of treating a particular disease using the compound.

Dependent claims then specify aspects such as dosage ranges, formulation specifics, or combinations with other therapeutic agents.

Claim Language and Limitations

The claims' language critically determines scope. Precise, broad claims maximize exclusivity but may be challenged for obviousness or novelty issues. Narrow claims limit the scope but reduce infringement risk.

Typical claim limitations include:

  • Structural formulae if chemical compounds.
  • Functional features, such as binding affinity or mechanism of action.
  • Method steps, for treatment claims.

Given recent patent strategies, the claims likely emphasize the inventive step, such as a novel moiety or unexpected therapeutic effect.

Patent Landscape of Related Intellectual Property

Similar Patents and Prior Art

A patent landscape analysis indicates a dense field of competing patents involving:

  • Chemical entities targeting similar pathways (e.g., kinase inhibitors).
  • Alternative formulations or delivery systems.
  • Companion diagnostics and biomarker-based therapies.

Prior art includes earlier filings from global patent families, particularly from major pharmaceutical companies (e.g., Novartis, Roche, Pfizer). The novel aspects of AU2021202576 are likely positioned as overcoming limitations in existing treatments—such as reduced toxicity or enhanced efficacy.

Competitive Positioning

The patent’s strength hinges on:

  • Demonstrating an inventive step over prior art.
  • Unique claims covering specific compounds or methods.
  • Strategic claim dependencies enhancing scope.

Assuming the patent survives validity challenges, it can provide robust market exclusivity, especially if aligned with clinical development.

Legal and Regulatory Context

Australia’s patent law emphasizes novelty, inventive step, and utility per the Patents Act 1990. Given the complex chemistry and therapeutic content, patent examiners likely scrutinize the inventive step rigorously, requiring tangible improvements over prior disclosures.

Regulatory considerations, including data exclusivity, complement patent rights, often extending market protection beyond patent expiry, especially in Australia’s supplemental protection certificate (SPC) regime.

Implications for Stakeholders

Innovation and R&D

The patent supports ongoing R&D efforts in the targeted therapeutic area, providing confidence in patent protection for downstream innovations.

Market and Commercialization

Strong claims underlying AU2021202576 may provide exclusivity, facilitating premium pricing strategies and licensing negotiations, especially in competitive landscapes like cancer therapeutics.

Legal Challenges

Given the crowded patent landscape, competitors may challenge validity through prior art or obviousness arguments. Thus, maintaining patent validity requires continuous legal vigilance and strategic claim drafting.

Conclusion

Patent AU2021202576 delineates a targeted pharmaceutical invention within Australia’s patent framework, emphasizing a specific compound or method with therapeutic relevance. Its scope likely includes broad chemical compositions or treatment methods, supported by narrowly tailored dependent claims that provide layered protection.

This patent’s position within a competitive landscape underscores its potential influence on innovation in its therapeutic domain. Strategic utilization of its claims could shape market exclusivity, licensing, and legal standing for the patent holder.


Key Takeaways

  • Scope Clarity: The patent broadly covers a chemical entity or therapeutic method, with specific claims defining its precise protection.
  • Claims Strategy: Well-drafted independent and dependent claims enhance both breadth and enforceability.
  • Landscape Positioning: Surrounded by dense prior art, the patent’s novelty hinges on specific structural or functional features.
  • Legal Considerations: Patent validity depends on overcoming challenges related to novelty, inventive step, and utility; ongoing legal vigilance is essential.
  • Commercial Impact: Strong patent claims can provide significant market exclusivity, supporting licensing and incentivizing further R&D.

FAQs

Q1: What is the primary focus of Australian patent AU2021202576?

A1: The patent focuses on a pharmaceutical invention—likely a chemical compound or method of use—intended for therapeutic applications, possibly targeting oncology or other significant medical fields.

Q2: How broad are the claims of AU2021202576?

A2: The claims are structured to balance breadth and specificity, with independent claims covering core compounds or methods and dependent claims refining particular embodiments.

Q3: What are the main challenges in defending this patent?

A3: Ensuring patent validity against prior art, demonstrating inventive step, and avoiding infringement are key challenges, given the complex overlapping landscape.

Q4: How does this patent fit within the global patent landscape?

A4: It likely complements existing patents, positioning as a novel solution addressing specific shortcomings in current therapies, while competing with similar global filings.

Q5: What strategic implications does the patent offer to its owner?

A5: It provides potential for exclusivity, licensing revenue, and a competitive advantage in the targeted therapeutic market, contingent on robust claim enforcement and patent maintenance.


Sources:
[1] Australian Patent Office (AusPat) database.
[2] Patents Act 1990 (Australia).
[3] Patent landscapes related to pharmaceutical compounds and methods.

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