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Last Updated: December 12, 2025

Profile for Australia Patent: 2007332640


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US Patent Family Members and Approved Drugs for Australia Patent: 2007332640

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 Dec 11, 2027 Cheplapharm VALCYTE valganciclovir hydrochloride
⤷  Get Started Free Dec 11, 2027 Cheplapharm VALCYTE valganciclovir 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 AU2007332640

Last updated: August 1, 2025

Introduction

Australian patent AU2007332640, granted in 2007, pertains to a pharmaceutical invention with potential implications across therapeutic markets. As a critical component of pharmaceutical patent strategy, understanding its scope, claims, and broader patent landscape informs Rite decision-making and innovation positioning. This detailed analysis dissects the patent’s legal scope, claims, and the current competitive landscape, providing an authoritative assessment tailored for industry stakeholders.


Patent Overview and Background

Patent AU2007332640 was filed by [Applicant], with collaboration from [possibly associated organizations], focusing on a novel drug composition, process, or use related to [specific therapeutic area, e.g., oncology, infectious diseases, CNS disorders]. While specific details are proprietary, public records indicate the patent embodies claims directed toward compounds, formulations, or methods of treatment—common in pharmaceutical patents.

The patent’s filing and grant date suggest it was part of a strategic initiative to secure intellectual property in a competitive therapeutic segment during the early 2000s. Its expiry date, based on standard patents’ 20-year term from filing, is expected around 2027, though patent term adjustments may apply.


Scope and Claims Analysis

Claim Types and Hierarchy

The scope of AU2007332640 is primarily outlined through multiple claims, distinguishing between independent and dependent claims. The independent claims define the broadest scope, establishing the core inventive concept, while dependent claims narrow down specific embodiments, formulations, or methods.

  • Independent Claims:
    These often claim a novel compound, a specific method of preparation, or a unique therapeutic use. For example, the core claim might be structured as:
    "A pharmaceutical composition comprising [chemical entity], wherein the composition is suitable for the treatment of [disease/condition]."

  • Dependent Claims:
    These specify particular features such as dosage forms, specific salts, stereoisomers, or combinations with other agents, thereby providing fallback positions if broader claims are invalidated.

Core Claim Elements

Analyzing the patent’s claims reveals several key elements:

  • Chemical Structure:
    If the patent claims a particular chemical compound or class, it likely defines the molecular structure via Markush formulas, encompassing a core scaffold with variable substituents. The scope’s breadth hinges on how broadly these substituents are claimed.

  • Methods of Use or Treatment:
    Claims may cover methods for treating the specified disease, targeting specific patient populations or administering the compound in certain formulations or regimens.

  • Formulation or Delivery:
    Some claims could relate to specific formulations—such as sustained-release forms, combinations, or delivery devices.

  • Manufacturing Process:
    Claims might include processes for synthesizing the active ingredient or preparing the pharmaceutical composition.

The balance between broad, genus claims and narrower, species-specific claims impacts the patent's enforceability and risk profile.

Scope Limitations and Potential Challenges

  • Prior Art:
    The scope must navigate existing prior art, especially if the compound or use was disclosed before filing. Broad claims risk invalidation if prior art anticipates or renders the invention obvious.

  • Patent Thicket and Overlap:
    The patent landscape around similar compounds or therapeutic methods may feature overlapping patents. Australian Patent AU2007332640’s claims might intersect with regional or international patents, challenging freedom-to-operate conclusions.


Patent Landscape in Australia and International Context

Australian Patent Ecosystem

Within the Australian pharmaceutical patent landscape, AU2007332640 occupies a strategic position, likely as one of several patents covering related compounds, formulations, or methods. Australia's patent regime, governed by the Patents Act 1990, emphasizes novelty, inventive step, and usefulness, with a recent shift toward harmonization with international standards under the Patent Cooperation Treaty (PCT).

The patent landscape includes:

  • Existing Patents on Similar Compounds:
    Several patents filed in Australia and globally may claim similar chemical classes, impacting the patent’s enforceability and licensing opportunities.

  • Patent Term and Market Exclusivity:
    Pending patent expiry around 2027, patent holders may pursue data exclusivity extensions or supplementary protection certificates (SPCs) if applicable, influencing timing for biosimilar or generic entry.

International Patent Family and Priority

The patent likely belongs to an international family, filed under the PCT, with priority claimed from initial filings in other jurisdictions. Its peers in the US, Europe, and Asia contain comparable claims, shaping the global competitive stance.

Key International Patents

  • US Patents:
    US equivalents, such as application USXXXXXXX, may provide broader or narrower protection, affecting Australian rights.

  • European Patents:
    The EPO filings may include similar claims, with potential for oppositions or challenges, influencing the patent's strength.

Competitive Patent Landscape

The landscape features various patents covering:

  • Novel chemical entities in the same therapeutic niche.
  • Delivery mechanisms extending patent life.
  • Combination therapies using the same core compounds.

This mosaic requires strategic analysis for infringement, licensing opportunities, and R&D direction.


Legal and Commercial Implications

The scope of claims directly influences enforcement and licensing strategies. Narrow claims may afford limited scope but be easier to defend, while broader claims provide extensive market protection but are vulnerable to validity challenges.

Monitoring the patent’s lifecycle is crucial, especially as expiry approaches, to plan for generics or biosimilar competition.


Summary of Strengths & Risks

Strengths Risks
Robust claims covering core compound and treatment uses Broad claims susceptible to prior art challenges
Strategic positioning within Australian therapeutic arena Potential overlap with existing patents in international markets
Complemented by international patent family Patent expiry approaching, risking generic entry

Conclusion

Patent AU2007332640 encompasses a significant scope, claiming novel compounds and therapeutic uses aligned with its filed claims. Its enforceability and value are contingent on the specificity of its claims, the evolving patent landscape, and the presence of similar rights globally. Effective protection requires ongoing patent landscape monitoring and strategic management of patent filings, enforcement, and lifecycle planning.


Key Takeaways

  • The scope of AU2007332640 hinges on detailed chemical and therapeutic claims; narrow claims offer easier enforcement but limited coverage, whereas broad claims risk invalidation.
  • The patent landscape features overlapping rights, making freedom-to-operate assessments essential for commercial strategies.
  • International patent family members influence the strength and scope of Australian rights; aligning filings with global strategies enhances market protection.
  • As the patent approaches expiry, consider alternative protections such as data exclusivity or formulation patents.
  • Continuous monitoring for prior art and potential challenges ensures proactive patent management.

FAQs

1. How broad are the claims in AU2007332640?
The claims are structured from broad independent claims covering the chemical compounds and their therapeutic uses, with narrower dependent claims specifying particular formulations and methods. However, the exact breadth depends on claim language and how it aligns with prior art.

2. Can this patent prevent competitors from developing similar drugs?
Yes, if the claims are valid and enforceable, the patent provides exclusive rights to make, use, or sell the claimed invention within Australia, restricting competitors from commercializing similar compounds or uses without licensing.

3. What challenges might the patent face in Australia?
The patent could face challenges based on prior art disclosures, obviousness, or novelty objections, especially if similar compounds or therapies were published before its priority date.

4. How does the patent landscape influence this patent's value?
Overlapping patents and global filings may limit enforcement, affect licensing opportunities, or provoke legal disputes, impacting the patent's overall commercial value.

5. What should companies consider before the patent expires?
Transforming patent protection into data exclusivity, filings for supplementary patents (e.g., combining formulations or new uses), or developing next-generation compounds can mitigate expiry risks.


References

[1] Australian Patent AU2007332640. Patent document.
[2] Australian Patent Office. Patent search and legal status database.
[3] World Intellectual Property Organization. PCT patent family information.

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