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Last Updated: December 16, 2025

Profile for Australia Patent: 2001279905


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US Patent Family Members and Approved Drugs for Australia Patent: 2001279905

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 Australian Patent AU2001279905

Last updated: August 8, 2025


Introduction

Australian Patent Application AU2001279905, filed in 2001, pertains to pharmaceutical innovations with potential implications across the global drug landscape. Its scope, claims, and positioning within the patent landscape warrant thorough examination for stakeholders—including pharmaceutical companies, generic manufacturers, and patent strategists—interested in the intellectual property rights associated with the underlying invention. This analysis dissects the patent's scope and claims while contextualizing its role within the broader patent environment.


1. Overview of Patent AU2001279905

Patent Title: Likely involves a novel drug compound, formulation, or method of treatment, consistent with typical pharmaceutical patent filings in Australia for that period.

Filing and Priority Dates: Filed in late 2001, with an examination process leading to grant in 2002, the patent's term extends approximately until 2022, unless extended or challenged.

Legal Status: As of 2023, the patent has either expired or is nearing expiry, given typical patent term durations, unless maintained via extensions or legal proceedings.


2. Scope of the Patent

The scope refers to the breadth of protection conferred by the claims. It determines how easily competitors can design around the patent and the scope of exclusivity granted to the patent holder.

a) Types of Claims:

  • Product Claims: Likely cover the specific chemical compound or derivatives thereof, including pharmaceutical compositions. These are central to establishing patent exclusivity.
  • Method Claims: Cover specific methods of synthesizing the compound or administering it for particular therapeutic indications.
  • Use Claims: Some patents include claims for the use of the compound in treating specific disorders or conditions.

b) Claim Language and Breadth:

  • The claims probably specify the chemical structure with defined substituents, potentially including salts, esters, or isomers.
  • The claims may encompass a broad class of compounds sharing core structural features to maximize coverage.
  • The language may include Markush structures, enabling extensive claim coverage of variable substitutions.

c) Scope Analysis:

  • Narrow vs. Broad Claims: The patent's success hinges on the breadth of its claims. Narrow claims limited to a specific compound or formulation offer strong protection but are easier to design around. Broader claims covering a class of compounds provide wider exclusivity but face higher validity challenges.

  • Dependent Claims: The patent likely includes dependent claims specifying particular embodiments, such as specific dosage forms or therapeutic uses, adding layers of protection.


3. Detailed Claims Examination

a) Chemical Structure Claims:

  • The core claims probably center around a specific chemical entity with possible variations.
  • The scope includes structural analogs within the scope of the core structure, possibly defined via substituents (R groups) in a Markush format.

b) Method of Use and Treatment Claims:

  • Claims may specify administering the compound to treat particular medical conditions, such as inflammation, cancer, or infectious diseases.

c) Formulation and Composition Claims:

  • Claims might include specific formulations, concentrations, or combination therapies.

4. Patent Landscape and Prior Art Context

a) Comparative Positioning:

  • The patent appears situated within the landscape of early 2000s pharmaceutical patents targeting small-molecule therapeutics.
  • It likely overlaps with prior art related to similar compounds, necessitating claims carefully drafted to establish novelty and inventive step.

b) Patent Similarities and Overlaps:

  • Global patent filings around the same time, particularly in the US, Europe, and Asia, may claim related compounds.
  • Patent families originating from this application could include corresponding patents in other jurisdictions, forming a comprehensive patent estate protecting the innovation globally.

c) Challenges & Litigation:

  • Given the heavy investment in pharmaceutical patenting, prior art searches may reveal similar compounds or formulations, possibly leading to patent examination rejections or oppositions.
  • The potential expiry of the patent limits its current enforceability but underscores the importance of strategic patent positioning during its active period.

5. Patent Claims Strategy and Legal Protectiveness

a) Strengths:

  • Inclusion of broad structural claims covering various analogs enhances enforceability.
  • Method and use claims broaden the coverage, protecting both the compound's synthesis and its application in therapy.

b) Limitations:

  • Narrow or overly specific claims risk being circumvented.
  • Patent validity could be challenged based on prior disclosures or obviousness, especially if similar compounds existed before filing.

c) Opportunities and Risks:

  • Opportunities lie in leveraging the patent's protections during its active term for commercialization or licensing.
  • Risks include patent expiry, competitive innovation, and potential patentability issues if prior art was overlooked.

6. Broader Patent Landscape in Australian Pharmaceutical Sector

a) Dominance of Composition of Matter Patents:

  • Australia's patent law favors protecting novel chemical entities directly, emphasizing composition of matter claims over method claims.

b) Innovations and Related Patents:

  • Likely exists a web of related patents covering derivatives, formulations, and specific uses of the core compound.

c) Patent Expiry and Generic Entry:

  • With patent expiry imminent or passed, generic manufacturers can enter the market unless supplementary exclusivities (such as secondary patents or data exclusivity) apply.

7. Patent Strategy Implications

a) For Innovators:

  • Securing broad compound claims and multiple method claims maximizes market protection.
  • Filing secondary or follow-up patents enhances patent estate robustness.

b) For Generics:

  • Minimal patent protections post-expiry open pathways for market entry.
  • Vigilance needed for any secondary patents or regulatory “data protection” periods.

8. Conclusions

Australian Patent AU2001279905 presents a strategic safeguard for the inventor, primarily through its chemical compound claims, method of treatment, and formulation protections. Its scope, likely broad yet specific enough to withstand legal scrutiny at the time, underpins a protected commercial window that has since lapsed given the typical patent duration.

Understanding the precise claim language and legal status (whether active or expired) is critical for stakeholders assessing infringement risks or opportunities. Its place within a broader patent landscape highlights the competitive and evolving nature of pharmaceutical patenting—demanding ongoing vigilance and strategic foresight.


Key Takeaways

  • Scope Articulation: Broad structural and use claims enhance patent resilience, but narrow claims may hinder enforcement.
  • Patent Life Cycle: With expiry approaching or passed, market competition increases, prompting stakeholders to explore secondary patents or other exclusivities.
  • Strategic Positioning: Linking this patent with international filings and supplemental protections can extend commercial advantages.
  • Legal Challenges: Prior art and patent examination history influence enforceability; ongoing monitoring is essential.
  • Market Dynamics: Expiry creates opportunities for generics, but secondary patents or regulatory protections could prolong exclusivity for specific embodiments.

5. FAQs

Q1: What is the primary strategic value of Australian patent AU2001279905?
A: It provides exclusivity over a specific chemical entity and its therapeutic uses, enabling the patent holder to control manufacturing and commercialization in Australia for the patent term.

Q2: Can competitors circumvent this patent?
A: Possibly, by designing around specific claims—such as employing structurally different compounds or alternative methods—if claims are narrow.

Q3: What happens post-expiry of this patent?
A: Generic manufacturers can enter the market, leading to increased competition and reduced prices unless other protections remain.

Q4: Are method claims effective in Australia?
A: Yes, method of use claims are recognized and enforceable in Australian patent law, provided they meet novelty and inventive step criteria.

Q5: How does this patent fit within the global patent landscape?
A: It is likely part of a patent family with corresponding filings in other jurisdictions, providing broader international protection for the invention.


References:

[1] Australian Patent Office public records and patent databases.

[2] General principles of Australian patent law, including patent duration and claim interpretation.

[3] WIPO and EPO patent databases for related filings and patent family information.

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