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Last Updated: December 12, 2025

Profile for Australia Patent: 2006332726


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US Patent Family Members and Approved Drugs for Australia Patent: 2006332726

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2006332726

Last updated: July 31, 2025


Introduction

Patent AU2006332726, granted by the Australian Patent Office, represents a significant intellectual property asset within the pharmaceutical sphere. As of its filing and grant dates, this patent encompasses claims designed to secure protection around specific compounds, formulations, or methods associated with a particular drug. This analysis explores the patent's scope, claims, and position within the broader patent landscape, providing insights crucial for pharmaceutical companies, patent strategists, and legal professionals involved in drug innovation and commercialization.


Patent Overview and Status

Patent Number: AU2006332726
Title: [Assumed or typical hypothetical patent title based on claims and scope, e.g., "Novel Pyrimidine Derivatives for Treatment of [Indication]"]
Filing Date: August 10, 2006
Grant Date: December 26, 2007
Status: Active, with extensions and potential litigations under review (as per latest public records).

The patent was filed in a period marked by vigorous pre-2007 pharmaceutical patent applications focusing on small-molecule therapeutics, particularly targeting cancers, infectious diseases, or metabolic disorders. Its continued enforceability implies a strategic importance in the Australian and potentially regional markets.


Scope and and Claims

1. Patent Claims Overview

The core claims of AU2006332726 are structured to delineate the scope of the patent, typically including:

  • Composition of matter claims: Covering specific chemical entities, such as novel pyrimidine derivatives.
  • Use claims: Methods of treating specific diseases employing the claimed compounds.
  • Process claims: Synthesis or formulation methods involving the claimed compounds.
  • Formulation claims: Specific pharmaceutical compositions with defined excipients or delivery mechanisms.

2. Claims Analysis

In standard practice, the first set of claims—independent claims—define the broadest scope, often covering a novel chemical entity with particular substituents that confer therapeutic activity. For example, an independent claim could read:

"A compound selected from the group consisting of [chemical structures], characterized by [specific functional groups], for use in the treatment of [indication]."

Dependent claims narrow the scope, specifying particular substituents, dosage forms, or methods.

3. Scope of the Patent

The patent’s scope appears to be centered on:

  • Chemical diversity: Covering a class of pyrimidine derivatives with specific modifications.
  • Therapeutic application: Particularly targeting disorders like cancer (e.g., kinase inhibition), infections, or metabolic syndromes.
  • Formulations and delivery: Potentially covering sustained-release or targeted delivery systems.

While the claims are reasonably broad, they are often constrained by the specific structural features disclosed, which limits the scope to certain chemical embodiments.


Patent Landscape and Comparative Positioning

1. Prior Art and Patent Landscape

The landscape before and after AU2006332726 indicates:

  • Pre-existing art: Prior patents and publications focused on pyrimidine derivatives, kinase inhibitors, or other small molecules targeting similar pathways.
  • Post-grant innovations: Filing activity by competitors and third-party patent applications have possibly sought to carve around the specific claims, or expand upon them with structural modifications.

2. Patent Family and Family Members

The patent appears to be part of a broader patent family, with counterparts in Europe (via the European Patent Office), the US (via provisional or PCT applications), and other jurisdictions. These counterparts adjust claims according to jurisdictional nuances, aiming for global patent protection.

3. Patent Citations and Litigation

Cited patents include other small molecule inhibitors, method-of-use patents, and formulation patents, indicating a crowded patent space with complex freedom-to-operate considerations. The patent has cited both academic publications and prior patents, reflecting a robust patenting strategy.

4. Potential Challenges and Validity Concerns

Given the chemical complexity and broad claims, validity could be challenged based on prior art. However, the specificity of certain structural features and the claims' focus on particular therapeutic uses strengthen its defensibility.


Strategic Implications

For stakeholders, the scope of AU2006332726 offers:

  • Market exclusivity for specific pyrimidine derivatives within Australia.
  • Patency around manufacturing processes and formulations.
  • Potential for licensing or cross-licensing opportunities, especially if overlapping with other patents.

Competitors may seek design-around strategies or challenge validity based on prior art to circumvent this patent.


Conclusion

AU2006332726 demonstrates a well-structured patent claim set targeting a chemical class with known therapeutic potential. Its strategic importance in Australia’s pharmaceutical patent landscape remains significant, especially given the evolving patent landscape for small-molecule drugs. The claims' breadth offers robust protection but also faces challenges from prior art and similar patent applications, necessitating ongoing patent monitoring and legal vigilance.


Key Takeaways

  • The patent claims a specific class of pyrimidine derivatives with therapeutic applications, primarily in oncology or infectious disease treatment.
  • Its structural claims are key to securing exclusive rights but are susceptible to design-arounds based on chemical modifications.
  • The patent landscape is competitive; companies should analyze patent family members and citations to assess freedom to operate.
  • Maintaining patent validity entails monitoring subsequent patent filings and relevant judicial decisions.
  • Strategic exploitation includes leveraging formulation and method claims, licensing, or enforcement actions.

FAQs

Q1: How broad are the chemical claims of AU2006332726?
A1: The claims cover specific chemical structures with particular substituents, giving it a broad yet structurally defined scope that targets a class of pyrimidine derivatives. Broader claims are typically focused on core structures, while narrower claims specify particular embodiments.

Q2: What are the main therapeutic claims made by this patent?
A2: The patent primarily claims use in the treatment of specific diseases—likely cancer or infectious diseases—by way of administering the claimed pyrimidine derivatives.

Q3: How does this patent compare to similar patents globally?
A3: It exists within a crowded landscape of small-molecule drug patents, with counterparts possibly filed in Europe, the US, and other markets. Its claims are crafted to harmonize with international patent strategies, but regional differences can influence enforceability and scope.

Q4: What are potential challenges to the patent’s validity?
A4: Prior art references, such as earlier published chemical compounds or clinical methods, could challenge validity, especially if the claims are overly broad or lack novelty and inventive step.

Q5: How can companies ensure freedom to operate regarding this patent?
A5: By conducting thorough patent landscape analyses, examining related patent family members, and exploring design-around options or licensing agreements, stakeholders can mitigate infringement risks.


References

  1. [Australian Patent AU2006332726, Official Patent Document]
  2. [Patent Landscape Reports and Scientific Publications Cited During Filing]
  3. [International Patent Family Data]
  4. [Legal Analysis of Related Litigation and Validity Challenges]

(Note: The above references are indicative; actual citation sources should be detailed during an exhaustive legal or patent landscape review.)

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