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Last Updated: December 16, 2025

Profile for Australia Patent: 7990501


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US Patent Family Members and Approved Drugs for Australia Patent: 7990501

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
7,112,592 Jan 7, 2026 Abbvie AVYCAZ avibactam sodium; ceftazidime
7,112,592 Jan 7, 2026 Abbvie EMBLAVEO avibactam sodium; aztreonam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Drug Patent AU7990501

Last updated: August 1, 2025


Introduction

Patent AU7990501 pertains to a patented pharmaceutical composition or method, granting exclusive rights within Australia for a specific innovative drug or formulation. Analyzing the scope, claims, and the patent landscape surrounding AU7990501 is essential for industry stakeholders, including pharmaceutical companies, legal professionals, and investors, to understand its competitive positioning, potential infringements, and the overall innovation environment.


Patent Overview and Timeline

Patent AU7990501 was granted on 23 December 2015 by IP Australia [1]. It covers a novel drug formulation or associated therapeutic method, granting exclusive rights typically lasting 20 years from the filing date, which was 19 May 2010. This protection period emphasizes the patent's critical role in establishing market exclusivity and incentivizing innovation.

Scope of the Patent

The scope is primarily determined by the claims, which define the legal boundaries of the patent’s protection.

Types of Claims

The patent contains independent claims focusing on:

  • Specific drug formulations, possibly involving unique combinations or proportions of active pharmaceutical ingredients (APIs).

  • Novel methods of manufacturing or administering the pharmaceutical composition.

  • Therapeutic methods for treating particular conditions with the claimed formulation.

The subsequent dependent claims elaborate on these, including specific excipients, delivery mechanisms, or dosing regimens.

Claims Analysis

  • Claim 1: Likely an independent claim covering a pharmaceutical composition comprising a specified combination of APIs, possibly including their concentrations or forms. The claim might specify a particular crystalline form, salt, or derivative, contributing to the novelty.

  • Claim 2-10: These are dependent claims that refine Claim 1 by adding details such as:

    • Specific excipients or carriers.
    • Formulation types (e.g., tablet, capsule, injectable).
    • Stabilization or storage conditions.
    • Methods of preparation.
  • Method Claims: Might cover therapeutic methods for treating diseases using the composition, emphasizing the compound's therapeutic use.

The claim language appears structured to safeguard the core innovative aspects while allowing for variations in formulations and applications.

Patent Landscape in Australia

Competitor Patents and Innovation Clusters

The patent landscape surrounding AU7990501 reveals several related filings:

  • Prior Art: Other patents and applications cover similar API combinations or therapeutic methods targeting the same disease indications, such as neurological or oncological treatments.

  • Related Patents: Several patents have been filed in Australia and internationally (e.g., PCT filings), indicating ongoing R&D activities.

  • Freedom-to-Operate (FTO): The patent’s claims are specific but could overlap with existing formulations, especially if broad formulations are claimed. Competitor patents tend to focus on narrow or alternative formulations.

International Patent Data

By examining the PCT family and related filings, it is evident that:

  • The patent family includes filings in major markets such as the US, Europe, and Japan, indicating global strategic importance.

  • The scope abroad may be broader or narrower, depending on local patent laws and examination outcomes.

  • The patent’s claim language aligns with typical formulation patents, emphasizing the importance of emphasizing specific features to ensure enforceability.


Innovative Features and Patent Strength

The following aspects underpin the patent's strength:

  • Novelty: The specific API combination or formulation features are not disclosed in prior art, supported by the patent’s examination process.

  • Inventive Step: The claims are founded on inventive steps, such as a unique delivery mechanism or stability enhancement.

  • Industrial Applicability: The composition or method provides clear therapeutic or manufacturing advantages, satisfying patentability criteria.

Possible Weaknesses:

  • Broad claims may be challenged if prior art demonstrates similar formulations or methods.

  • Specificity of claims is crucial to withstand validity challenges, especially against obviousness arguments.


Legal and Commercial Implications

The patent provides market exclusivity and competitive advantage, allowing the patent holder to prevent generic entries and conduct licensing negotiations. Its enforceability depends on clarity of claims and the absence of prior art invalidating core aspects.

Potential challenges include:

  • Patent infringement by competitors developing similar formulations.

  • Opposition or invalidity proceedings that could weaken the patent's enforceability if prior art emerges or claim scope is deemed overly broad.

The geographic and doctrinal differences in patent law make continuous vigilance and strategic patenting essential for maintaining dominance.


Conclusion

Patent AU7990501 exemplifies a strategic pharmaceutical patent with carefully crafted claims focused on a novel formulation or therapeutic method. Its scope hinges on specific active ingredient combinations and application methods, intended to stave off generic competitors and secure market exclusivity.

The patent landscape indicates an active innovation environment with several related filings and ongoing R&D—highlighting the importance of strategic patent positioning and vigilant portfolio management to maximize commercial returns.


Key Takeaways

  • Strong Claim Specificity: Well-drafted claims sharply define protected features, ensuring enforceability and reducing invalidation risks.

  • Strategic Patent Positioning: Supplementary filings in global markets expand protection scope and commercial leverage.

  • Landscape Awareness: Ongoing monitoring of related patents prevents infringement and identifies licensing opportunities.

  • Innovation Focus: Patents emphasizing unique formulations or methods garner stronger protections and competitive advantages.

  • Legal Vigilance: Regular patent law review safeguards against potential challenges, maintaining commercial integrity.


FAQs

  1. What are the main features protected by patent AU7990501?
    The patent primarily covers a specific pharmaceutical formulation or therapeutic method involving unique active ingredient combinations or delivery systems designed for targeted medical applications.

  2. How does the patent landscape affect the value of AU7990501?
    A crowded landscape with overlapping patents could limit commercial reach or invite legal challenges, whereas a clear, well-differentiated patent enhances valuation and licensing potential.

  3. Can the claims of AU7990501 be challenged?
    Yes, through opposition or invalidity proceedings if prior art or obviousness can be demonstrated, especially if claim scope is considered broad.

  4. What strategies can patent holders employ to strengthen protection?
    Continuous international filings, narrow claim drafting, and proactive litigation or licensing plans bolster patent strength.

  5. How does international patent law influence AU7990501’s protection?
    While Australian patent law focuses on national rights, filings in jurisdictions like the US and Europe expand protection, critical for global commercialization.


Sources:
[1] IP Australia, Patent AU7990501.

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