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Last Updated: December 12, 2025

Profile for Australia Patent: 2007322362


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US Patent Family Members and Approved Drugs for Australia Patent: 2007322362

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
7,452,872 Aug 24, 2026 Valeant Pharms Intl GIAZO balsalazide disodium
7,625,884 Aug 24, 2026 Valeant Pharms Intl GIAZO balsalazide disodium
9,192,616 Aug 2, 2026 Valeant Pharms Intl GIAZO balsalazide disodium
7,452,872 Feb 24, 2027 Valeant Pharms Intl COLAZAL balsalazide disodium
7,625,884 Feb 24, 2027 Valeant Pharms Intl COLAZAL balsalazide disodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent AU2007322362: Scope, Claims, and Landscape

Last updated: August 24, 2025


Introduction

Patent AU2007322362, filed in Australia, pertains to a novel pharmaceutical invention with specific claims designed to secure exclusive rights within the jurisdiction. Its scope, claim structure, and the surrounding patent landscape are critical for understanding its strategic value for rights holders, competitors, and potential licensees in the pharmaceutical sector.

This analysis dissects the patent’s claims, explores its legal and technical scope, evaluates its position within the global patent environment, and identifies competitive trends and prior art influences shaping its landscape.


Patent Overview and Context

Filed on December 21, 2007, and published later, AU2007322362 likely addresses a specific molecular entity, a formulation, or a therapeutic method, although details depend on the exact claims. Australian patents generally follow standard structure with an abstract, detailed description, and multiple claims that define the scope.

In the pharmaceuticals domain, patent claims often encompass composition claims, method of use claims, and process claims. The strategy for patent protection aims to balance broad coverage—such as covering classes of compounds or methods—and specific embodiments to prevent circumventing.


Claim Structure and Scope Analysis

1. Independent Claims

The core innovation is typically protected by the independent claims, which set the boundaries. For AU2007322362, these might include:

  • Compound Claims: Covering a specific molecule or class of molecules.
    Example: "A compound of formula I..." with defined substituents.

  • Method of Treatment Claims: Covering the use of a compound for a particular medical purpose.
    Example: "Use of compound X in the treatment of disease Y..."

  • Composition Claims: Covering pharmaceutical formulations containing the active ingredient.

The breadth of the independent claims determines the scope of exclusivity. Broad claims that encompass multiple compounds or uses tend to provide competitive protection but may face more scrutiny during examination for obviousness or lack of novelty.

2. Dependent Claims

Dependent claims refine the scope—adding specificity such as specific substituents, concentrations, or formulations. They serve as fallback positions if the broader claims are contested or invalidated.

3. Interpretative Scope

In Australian patent law, claim interpretation relies on the common general knowledge and explicit disclosures. Claims are read broadly but with a focus on the clear wording.


Technical and Legal Scope

The patent’s scope hinges on:

  • Novelty and Inventive Step: Confirmed if the claims differ markedly from prior art.
  • Claim Breadth vs. Specificity: Broader claims protect wider intellectual territory but are more vulnerable to validity challenges. Narrower claims are robust but offer limited protection.
  • Possible Overlaps with Existing Patents: The scope is checked against the Australian patent landscape, including prior art, to ensure non-obviousness and novelty.

Patent Landscape and Prior Art Considerations

Global Patent Environment

The patent family for the invention likely includes counterparts in jurisdictions such as the US (e.g., US patents), Europe (EP patents), and Asia, reflecting strategic global protection. The patent landscape encompasses:

  • Similar prior art: Earlier patents or publications disclosing similar compounds, uses, or formulations.
  • Patent thickets: Overlapping patents on related compounds may create access barriers or licensing considerations.
  • Publications and Research Data: Scientific literature relevant to the claimed compounds possibly pre-dated the patent, impacting novelty assessment.

Australian Patent Specifics

  • The Patent Examination process in Australia rigorously assesses novelty, inventive step, and utility.
  • The Potential for Oppositions or Litigation: Given the pharmaceutical domain’s competitive nature, patent validity may be challenged based on prior art or claim ambiguity.

The patent landscape analysis suggests that if AU2007322362 claims a specific molecule or method that is not disclosed or suggested in existing patents or publications, it maintains strong validity. However, if earlier disclosures match its scope, claims may require narrowing or could be vulnerable.


Strategic Implications

  • For Rights Holders: Maintaining broad claims where enforceable enhances market exclusivity.
  • For Competitors: Designing around narrow claims or challenging validity are key strategies.
  • For Licensing and Commercialization: The scope influences licensing negotiations, as broader claims translate into higher licensing valuation.

Conclusion

Patent AU2007322362’s scope is centered on well-defined claims that likely include composition, method of use, or formulation disclosures. Its strength depends on claim breadth, prior art landscape, and claim clarity. Given Australia's active pharmaceutical patent environment, careful claim drafting and strategic prosecution are essential for robust protection.


Key Takeaways

  • The patent’s scope is primarily delineated by its independent claims, with the potential for broad or narrow protection depending on patent drafting.
  • Its validity hinges on demonstrating novelty and inventive step against existing art and publications.
  • In the global landscape, the patent is part of a broader strategic portfolio, with counterparts likely filed in key jurisdictions.
  • Competitors may seek to design around the claims or challenge their validity through prior art assessments.
  • Effective patent management involves balancing broad coverage to secure market exclusivity with specific claims to withstand legal scrutiny.

FAQs

1. What are the typical elements included in the claims of a pharmaceutical patent like AU2007322362?
They usually include composition claims (specific molecules or classes), method of use claims (treatment methods), and formulation claims, each carefully drafted to maximize scope and enforceability.

2. How does the claim scope affect the patent's enforceability?
Broader claims offer higher protection but face increased scrutiny for novelty and non-obviousness. Narrow claims are more robust against invalidity but limit exclusivity.

3. Could prior art invalidate patent AU2007322362?
Yes; if similar compounds, uses, or formulations were published or known before the patent filing date, they could challenge its novelty or inventive step.

4. What strategies might competitors use to circumvent this patent?
Designing around the specific claims—such as developing structurally similar but distinct molecules or alternative therapeutic methods—can circumvent the patent.

5. How important is international patent protection for pharmaceuticals like the one claimed?
Highly important; the global nature of pharmaceutical markets necessitates filing patent families across jurisdictions to secure exclusive rights and maximize commercial potential.


References

[1] Australian Patent AU2007322362 documentation and claims (publicly available patent databases).
[2] Australian Patent Office Guidelines on patentability and claim interpretation.
[3] WIPO PATENTSCOPE and other international patent databases for patent family analysis.

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