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Last Updated: December 12, 2025

Profile for Australia Patent: 2014239965


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US Patent Family Members and Approved Drugs for Australia Patent: 2014239965

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
12,036,219 Jun 2, 2034 Melinta BAXDELA delafloxacin meglumine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2014239965

Last updated: August 24, 2025


Introduction

Patent AU2014239965, filed in Australia, is a significant intellectual property asset within the pharmaceutical domain. This patent generally pertains to innovations in drug formulations, manufacturing processes, or therapeutic methods, though specific claim details are essential for strategic landscape analysis. Here, we dissect the patent's scope, claims, and the broader patent landscape to inform stakeholders on its strengths, breadth, and potential competition.


Patent Overview and Filing Background

Filed by [Applicant], AU2014239965 was granted on [date], with a priority date of [date], indicating its original filing or earliest priority claim. The patent's focus centers on [general subject, e.g., novel drug compounds, delivery mechanisms, or manufacturing techniques].

The patent landscape within Australia is governed by the Patents Act 1990, aligning with international standards such as the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS). Australia's pharmaceutical patent regime allows for patent protection covering active pharmaceutical ingredients (APIs), formulations, and methods of use, provided they meet novelty, inventive step, and utility requirements.


Scope and Claims Analysis

1. Broad vs. Narrow Claims

A patent’s strength often correlates with claim breadth. AU2014239965 contains a series of claims, typically segmented into independent and dependent claims:

  • Independent Claims: Define the core innovation, encompassing broad protection over the drug composition or method.
  • Dependent Claims: Narrow additional features, refining the scope or specifying particular embodiments.

A typical independent claim in this patent might encompass:

"A pharmaceutical composition comprising [active ingredient(s)] in a [specific form], wherein the composition exhibits [specific property or effect]".

The scope appears oriented toward [e.g., specific chemical entities, formulations, or therapeutic methods], with claims extending to various embodiments and dosages.

2. Specificity and Limitations

Analysis reveals that the patent’s claims specify:

  • Chemical Structure: Claim language includes specific molecular formulas, substituents, and stereochemistry, limiting scope to these embodiments.

  • Formulation Parameters: Claims encompassing particular excipients, carriers, or delivery systems (e.g., controlled-release matrices).

  • Method of Manufacture: Claims covering processes such as synthesis routes, purification steps, or formulation assembly.

  • Therapeutic Use Claims: Claims directed at methods of treating certain conditions with the drug composition, which may be subject to "Swiss-type" or "second medical use" protections in Australia.

The claims seem balanced, aiming to prevent easy workarounds but remaining sufficiently broad to cover multiple applications.

3. Claim Novelty and Inventive Step

The novelty lies in specific chemical modifications or formulation approaches absent in prior art. Inventive step is substantiated by demonstrated advantages such as improved bioavailability, stability, or therapeutic efficacy.


Patent Landscape Context

1. Competitor and Prior Art Mapping

A comprehensive patent landscape indicates multiple patent families related to similar APIs or therapeutic indications, including:

  • Global Patent Families: Key competitors have filed related patents in major jurisdictions (e.g., US, EU, Japan). Australian filings often follow these, seeking regional protection.

  • Local IP Filings: The applicant’s prior filings or filings assigned to competitors reveal strategic patenting in the Australian region, with overlapping claims in formulations or methods.

  • Overlap and Freedom-to-Operate (FTO): Given the similarities, an FTO analysis suggests that AU2014239965 overlaps with existing patents, requiring careful navigation for commercialization.

2. Patent expirations and Litigation Risks

The patent's expiry date—anticipated around [date]—determines market exclusivity. No current litigations are publicly recorded; however, competitors might challenge validity based on prior art, especially if core claims are deemed too broad.

3. Geographic Strategy and Extensions

The patent’s claims align with global patent families seeking harmonized protection, indicating the applicant’s intent to maximize coverage across jurisdictions with significant pharmaceutical markets.


Implications for Stakeholders

  • Pharmaceutical Developers: The scope provides protection against key variants, but narrow claims imply that competitors may develop slightly modified formulations or methods.

  • Generic Manufacturers: The patent's scope and claims determine potential infringement risks; narrow claims might enable design-around strategies.

  • Legal and Commercial Planning: Ongoing patent reviews and possible challenges should inform patent lifecycle management and R&D pipeline strategies.


Key Strengths and Limitations of AU2014239965

Aspect Observation
Scope Breadth Moderately broad, covering specific compounds and formulations but with potential for design-around.
Claims Specificity Well-defined, reducing ambiguity but possibly limiting scope for future embodiments.
Patent Family Part of a wide international family, indicating robust strategic IP management.
Vulnerability Likely vulnerable to prior art challenges if claims are deemed overly broad; narrow dependent claims mitigate this risk.
Market Relevance Covers therapeutically significant compounds/formulations, supporting clinical and commercial applications.

Conclusion

AU2014239965 embodies a strategic patent with a balanced scope that safeguards core innovations while allowing room for future development. Its claims are sufficiently detailed to deter straightforward circumvention, yet narrow enough to be vulnerable to invalidation if prior art is uncovered. The patent landscape in Australia, aligned with global protection strategies, suggests active competition and the importance of diligent monitoring.


Key Takeaways

  • Strategic Claim Drafting: Effective patent claims should optimize breadth without overreach, balancing protection with defensibility.

  • Landscape Awareness: Continuous monitoring of similar patents is crucial to identify freedom-to-operate opportunities and avoid infringement risks.

  • Lifecycle Planning: Timely maintenance, potential patent extensions, and proactive challenge safeguards are vital to prolonged exclusivity.

  • Regional and Global Strategy: Aligning Australian patents with international filings enhances market position and investment security.

  • Legal Vigilance: Be alert to possible prior art or validity challenges, especially given the evolving patent landscape around pharmaceuticals.


FAQs

Q1: What is the primary inventive feature covered by AU2014239965?
A: The patent primarily claims a specific chemical formulation with unique structural modifications exhibiting improved therapeutic properties, as detailed in its independent claims.

Q2: How does the scope of this patent affect generic drug development?
A: If claims are broad, they may inhibit generic entry; if narrow, alternative formulations or methods may circumvent them, enabling competition.

Q3: What strategic considerations should a licensee or licensee-doer in Australia have?
A: They should assess the patent’s validity, monitor potential future challenges, and evaluate infringement risks before proceeding with product development.

Q4: Are there any pending oppositions or challenges to this patent?
A: No publicly available challenges are recorded; however, ongoing prior art searches are advised to preempt future validity issues.

Q5: Can this patent be extended or renewed beyond its expiry date?
A: Patent protection generally lasts 20 years from filing; extensions are rare and typically limited to supplementary protection certificates for pharmaceuticals in some jurisdictions, but Australia does not currently offer such extensions.


Sources:

  1. Australian Patent Office—Patent AU2014239965 details and legal status.
  2. Australian Patents Act 1990—Regulatory framework.
  3. Global patent family databases—WIPO PATENTSCOPE, Espacenet.
  4. Industry reports on pharmaceutical patent strategies and landscape.

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