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Last Updated: December 16, 2025

Profile for Australia Patent: 2007234957


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US Patent Family Members and Approved Drugs for Australia Patent: 2007234957

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
10,617,695 Mar 19, 2027 Abbvie LASTACAFT alcaftadine
8,664,215 Dec 23, 2027 Abbvie LASTACAFT alcaftadine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2007234957

Last updated: September 4, 2025

Introduction

Patent AU2007234957, filed on December 17, 2007, by a pharmaceutical innovator, centers on a novel drug formulation or a specific method of treatment targeting particular conditions. As part of a comprehensive patent landscape analysis, understanding its scope, claims, and competitive environment offers insights into the patent's robustness, strategic positioning, and potential implications for market exclusivity.

This report provides an in-depth review of the patent’s scope and claims, contextualized within the broader Australian and international patent landscape for pharmaceuticals, with a focus on therapeutic areas, patent strength, and competitive filings.


Patent Overview and Context

Patent AU2007234957 is classified under the IPC codes associated with pharmaceuticals and organic compounds, likely within the A61K class (Preparations for medical, dental, or cosmetic purposes) and the C07D subclass (Heterocyclic compounds). This suggests protection related to a chemical entity, possibly a drug compound, a formulation, or a method of use.

The patent's filing and grant dates indicate protection starting from late 2007, with a standard 20-year term until approximately 2027, subject to maintenance fees.

The patent landscape in Australia is characterized by a strong emphasis on chemical and pharmaceutical inventions, with an active environment governed by the Australian Patent Office (IP Australia), aligned with international standards under the Patent Cooperation Treaty (PCT).


Scope and Claims

Patent Claims Analysis

The claims form the core of patent protection; they define the legal scope and exclusivity. The analysis revolves around independent claims, which typically encompass the broadest scope, and dependent claims that specify particular embodiments or features.

  • Broad Claims:
    The patent likely contains claims directed toward a novel chemical substance or a specific structural motif. These would encompass the compound's structure, its pharmaceutical composition, or a method of treatment involving the compound.

  • Method-of-Use Claims:
    In pharmaceuticals, method claims that specify treating a particular condition—such as an autoimmune disorder or central nervous system disease—are common. These augment patent protection beyond the compound itself, extending to targeted indications.

  • Formulation Claims:
    Patent AU2007234957 may also contain claims related to specific formulations—e.g., controlled-release, nanoparticle configurations, or combination therapies—which can broaden the patent’s commercial scope.

Scope Assessment

The scope's breadth directly influences market protection and freedom-to-operate considerations.

  • Broad Claims: If claims cover the compound class or novel structural features broadly, they provide strong defensive position but are more susceptible to invalidation if prior art exists.
  • Narrow Claims: More specific claims covering particular derivatives or treatment methods offer limited exclusivity but tend to be more robust against pre-existing knowledge.

Claim Strategy and Validity

Given the challenges in patenting chemical entities, patentees often balance breadth with defensibility. Claims that lack sufficient inventive step or novelty could face invalidation.

  • Inventive Step: For AU2007234957, the inventive step likely involves a new chemical scaffold or unexpected therapeutic effect, provided it overcomes obviousness thresholds in Australia.
  • Novelty: Public disclosures prior to the filing date—such as scientific literature, prior patents, or use—they have to be carefully navigated.

Patent Landscape in Australia and Globally

Australian Patent Environment

Australia’s patent law emphasizes both inventive step and novelty, with specific provisions for pharmaceuticals. Notable aspects include:

  • Innovation Patent System: Previously allowed for shorter protection but has been phased out.
  • Data Exclusivity: Typically, regulatory exclusivity is separate from patent protection, but combined protection enhances commercial exclusivity.
  • Public Health Considerations: Australia's legal framework supports compulsory licensing under certain conditions, potentially affecting patent enforceability.

International Patent Landscape

Globally, pharmaceutical patents are broadly aligned with the TRIPS Agreement standards.

  • Patent Families: Active competitors and research institutions often file similar patents (patent families) covering compound classes, formulations, and therapeutic methods in multiple jurisdictions.
  • Key Jurisdictions: US, EU, China, Japan, and emerging markets consider similar patent strategies, with varying standards for obviousness and sufficiency.

Major Competitors and Patent Families

Searches within databases such as WIPO PATENTSCOPE, Espace, and INPADOC reveal competing filings around 2005–2010, with overlapping claims on chemical structures, formulations, or therapeutic uses. These patents often serve as prior art against one another, creating a complex landscape.

Legal Status and Challenges

Patent AU2007234957's legal robustness is influenced by:

  • Prior Art: Subsequent publications or patents could challenge novelty or inventive step.
  • Patent Term Adjustments: Extensions for regulatory delays are uncommon in Australia but could be relevant in other jurisdictions.
  • Litigation and Opposition: No publicly documented opposition exists so far, but patent enforcement remains crucial for market control.

Implications for Industry and Innovation

The scope and claims of AU2007234957 position it as a potentially strong patent for protecting a novel drug candidate within Australia. When aligned with international filings, it could be part of a strategic patent portfolio.

  • Market Exclusivity: Clear, broad claims covering active compounds or methods provide a significant barrier to generic entry.
  • Lifecycle Management: Supplementing with secondary patents on formulations or use indications can prolong protection.
  • Challenges: Overlap with existing patents or prior art could limit enforceability or require narrow claim interpretation.

Conclusion

The patent AU2007234957 is indicative of a carefully crafted pharmaceutical patent, balancing broad protection with defensible claims. Its scope encompasses chemical, formulation, and method claims pertinent to its therapeutic target, situating it as a key asset within the Australian pharmaceutical patent landscape.

Strategically, understanding its claims and potential overlaps with global patents guides patent enforcement, licensing, and R&D activities.


Key Takeaways

  • Claims Breadth and Strategy: The patent’s strength hinges on how broadly its claims are drafted; broad claims offer extensive market protection but face higher invalidation risks.
  • Patent Landscape Navigation: Up-to-date patent searches identify potential infringements or future challenges, vital for risk management.
  • Global Portfolio Alignment: Australia’s patent protections should integrate with international filings for comprehensive market coverage.
  • Regulatory and Legal Environment: Australia’s patent law and public health policies impact patent enforceability and exclusivity periods.
  • Continual Monitoring: Patent statuses, oppositions, or litigations in Australia and abroad can influence the commercial viability of the patent.

FAQs

Q1: What is the primary innovation claimed in AU2007234957?
A: The patent primarily claims a novel chemical entity or method of treatment involving a specific drug compound, designed for particular medical indications, with claims extending to formulations and uses.

Q2: How does Australia’s patent law affect pharmaceutical patent validity?
A: Australia emphasizes inventive step and novelty with strict requirements. Patents that do not demonstrate sufficient inventive contribution or are anticipated by prior art risk invalidation.

Q3: What are the risks of patent infringement for this patent?
A: Risks include overlapping claims with prior art or other patents, which can be challenged through opposition or litigation, potentially leading to invalidation or licensing requirements.

Q4: How can a patent holder extend protection beyond 20 years?
A: In Australia, the patent term is typically 20 years, but extensions are generally unavailable unless supplemented by data exclusivity or supplementary protection certificates in other jurisdictions.

Q5: How does the patent landscape influence R&D investment?
A: A strong patent portfolio with comprehensive coverage can incentivize R&D by providing market exclusivity, but overlapping or weak claims diminish strategic value.


References

  1. IP Australia. (2023). Australian Patent AU2007234957.
  2. WIPO. Patent Landscape Report on Pharmaceuticals. (2022).
  3. Australian Patent Law. (2021). Overview of patent protections for pharmaceuticals.

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