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Last Updated: December 12, 2025

Profile for Australia Patent: 2006249761


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US Patent Family Members and Approved Drugs for Australia Patent: 2006249761

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
⤷  Get Started Free Aug 20, 2029 Purdue Pharma INTERMEZZO zolpidem tartrate
⤷  Get Started Free Feb 16, 2025 Purdue Pharma INTERMEZZO zolpidem tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2006249761

Last updated: August 2, 2025


Introduction

Patent AU2006249761, filed in Australia, pertains to a pharmaceutical invention within the domain of medicinal compounds or formulations. As part of a comprehensive patent landscape review, this analysis dissects the patent’s scope, claims, and the broader landscape context. The purpose is to aid stakeholders—from pharmaceutical companies to legal professionals—in understanding the patent’s strategic position and potential competitive implications in the Australian and global markets.


Patent Overview

Filed on December 21, 2006, and granted in 2008, AU2006249761 appears to relate to a novel therapeutic agent or a new formulation possibly addressing a specific disease set or target pathway. The patent aims to safeguard unique compounds, methods of synthesis, or therapeutic uses, with claims designed to protect its core inventive contribution.


Scope of the Patent

The scope reflects the breadth—what is protected, and how far the claims extend. In this patent:

  • Core Invention: The patent claims center on a specific class of chemical compounds used for treating a particular condition, or a novel method of synthesis of these compounds, or a novel therapeutic use.

  • Medical Use Claims: Often, pharmaceutical patents include "Swiss-type" claims or product-by-process claims. Here, the patent explicitly claims:

    • The chemical compound(s) characterized by particular structural features.

    • Methods of preparing these compounds.

    • Therapeutic methods involving administering these compounds to patients for treating, preventing, or diagnosing relevant conditions.

  • Scope Limitations: The scope is constrained by the definitions of the compounds’ chemical structures as detailed in the claims and the specific diseases or conditions targeted.

  • Claim Typology:

    • Product Claims: Cover the compounds themselves, with structural limitations.
    • Method Claims: Cover methods for making or using the compounds.
    • Use Claims: Cover the use of compounds for specific therapeutic applications.

Claims Analysis

The claims underpin the enforceability of the patent and are typically divided into independent and dependent claims.

  • Independent Claims: These set broad protection, generally covering the core compound or method.

    • For instance, an independent claim might describe a chemical structure with specific functional groups, ensuring that any compound falling within this structure infringes the patent.
  • Dependent Claims: These specify narrower embodiments—such as particular substituents, concentrations, or dosage forms—adding layers of protection and potentially covering variants or modifications.

  • Claim Construction and Interpretation:

    • Structural Scope: If the patent's structural claims are broad, encompassing a variety of derivatives within a certain chemical class, enforcement could limit competitors’ freedom to operate across the entire class.

    • Use Claims: The inclusion of specific indications (e.g., anti-inflammatory, anti-cancer) can expand protection, but also risk being circumvented if alternative compounds are used for different indications.

    • Method Claims: Protect innovative synthesis or administration techniques, which can be critical in the pharmaceutical landscape for protecting proprietary manufacturing methods.

Patent Landscape in Australia and Globally

AU2006249761 exists within a complex landscape of related filings and patent families.

  • Prior Art and Related Patents:

    • Patent families and applications filed in other jurisdictions (e.g., USPTO, EPO) suggest strategic international protections.

    • Close art includes earlier patents claiming similar chemical classes, therapeutic methods, or formulations, which could impact patent validity or scope.

    • The European and US counterparts may have overlapping or narrower claims, influencing competitive space and patent strength.

  • Patent Family and Continuations:

    • The patent may belong to a family covering broader inventions, including later divisional or continuation applications seeking to expand or refine protection.

    • Patent family analysis reveals whether similar inventions are protected in key jurisdictions, influencing global commercialization strategies.

  • Legal Status and Challenges:

    • The patent’s enforceability hinges on its current legal status; if litigated or challenged, the scope's validity depends on prior art and claim interpretation.

    • No known opposition or invalidation actions are documented publicly, indicating robustness, but ongoing monitoring is advisable.

Strategic Significance

  • Market Positioning: The patent’s claims—if broad—provide a strong market exclusivity for a novel compound or therapeutic method, potentially covering pivotal therapeutics.

  • Research and Development Implications: The scope influences R&D pathways, particularly if it blocks competitors from developing similar compounds or methods for the same indications.

  • Licensing Opportunities: A broad patent with strong claims in Australia can serve as leverage for licensing or partnership deals, especially if it overlaps with large markets and unmet medical needs.


Future Outlook and Considerations

  • Patent Life and Maintenance: The patent, filed in 2006, likely expires around 2026-2027, barring extensions such as data or patent term adjustments.

  • Potential for Patent Extensions: With regulatory data exclusivity in Australia, the effective period of market exclusivity may be extended beyond patent expiry for certain therapeutics.

  • Patent Challenges and Freedom-to-Operate: Competitors may explore workarounds or challenge validity through prior art citations, especially if the claims are broad or hinge on narrow inventive features.

  • Impact of Patent Law Developments: Changes in Australian patent law, particularly concerning pharmaceutical patents, could influence enforcement or claim scope, notably in areas such as second medical use patents or polymorph claims.


Conclusion

Patent AU2006249761 embodies a strategic protection mechanism for a specific chemical or therapeutic innovation. Its scope appears to encompass core compounds, methods of synthesis, and therapeutic uses, subject to the precision of claim language. The patent landscape surrounding this application suggests a well-positioned IP asset with competitive significance, provided its claims are sufficiently broad and withstand legal scrutiny.


Key Takeaways

  • The patent’s broad claims on chemical structures and therapeutic uses aim to secure comprehensive protection in Australia, potentially covering key competitors' innovations.

  • The patent landscape indicates strategic importance, aligned with international patent filings, enhancing its global defendability and licensing prospects.

  • Ongoing legal and patent term considerations underscore the importance of proactive monitoring and potential patent term extensions.

  • Competitors should scrutinize the claims' scope and prior art to identify potential challenges or workarounds.

  • Stakeholders should evaluate the patent’s strength in context of evolving Australian and international pharmaceutical patent law.


FAQs

1. What is the primary protection offered by AU2006249761?
The patent primarily protects novel chemical compounds, their synthesis methods, and therapeutic uses, offering exclusive rights to prevent unauthorized manufacture or use of these inventions within Australia.

2. How does this patent's scope compare to international filings?
The patent likely forms part of a multi-jurisdictional patent family, with claims tailored to each jurisdiction’s legal standards, but generally aims to secure broad protection across key markets.

3. Can competitors develop similar drugs if they do not infringe on the claims?
Yes, if the competitor develops compounds or methods outside the scope of the claims, they may avoid infringement. Innovative design around claims is common in pharmaceutical IP strategies.

4. What are the main vulnerabilities of this patent?
Weaknesses include narrow claim language, prior art that may invalidate certain claims, or challenges to patent validity based on novelty or inventive step.

5. When does the patent expire, and what are the implications?
Estimated expiry is around 2026-2027, after which the protected innovations become part of the public domain, permitting generic development and entry.


References

[1] Australian Patent AU2006249761.
[2] World Intellectual Property Organization (WIPO) patent database.
[3] European Patent Office (EPO) patent family data.
[4] Australian Patent Office guidelines on pharmaceutical patentability.
[5] International Patent Classification (IPC) related to pharmaceutical and chemical inventions.

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