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Last Updated: December 16, 2025

Profile for Australia Patent: 2014329421


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US Patent Family Members and Approved Drugs for Australia Patent: 2014329421

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
⤷  Get Started Free Oct 2, 2034 Bausch JUBLIA efinaconazole
⤷  Get Started Free Oct 2, 2034 Bausch JUBLIA efinaconazole
⤷  Get Started Free Oct 2, 2034 Bausch JUBLIA efinaconazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2014329421

Last updated: August 24, 2025


Introduction

Patent AU2014329421, filed under the Patent Cooperation Treaty (PCT) system and subsequently granted in Australia, pertains to a pharmaceutical invention. Analyzing its scope, claims, and patent landscape reveals critical insights into its strategic positioning within the pharmaceutical intellectual property (IP) ecosystem, influencing market entry, licensing, and litigation prospects.


Patent Overview

Patent AU2014329421 was granted in Australia on [publication date] and relates to a novel compound, formulation, or method of use for treating specific diseases. The patent assignee appears to be a leading pharmaceutical entity, reflecting an innovative contribution within a therapeutically relevant class.

While precise patent specifications require detailed patent document review, the core scope generally encompasses claims directed at:

  • The chemical compound itself, including specific structural features.
  • Pharmaceutical compositions comprising the compound.
  • Methods of manufacturing the compound.
  • Therapeutic use, particularly in treating certain diseases or conditions.

A comprehensive understanding of the claims determines the patent’s strength and breadth, particularly in terms of exclusivity and potential infringement.


Scope and Claims Analysis

Claim Structure and Breadth

The patent’s claims are structured to balance breadth with specificity:

  • Independent Claims: Likely define the chemical compound (or class of compounds) with particular structural modifications, optimized for efficacy, stability, or bioavailability. These may include molecular formulas, stereochemistry, and specific substituents.
  • Method Claims: Cover specific methods of synthesizing the compound, formulations, or therapeutic methods (e.g., administering a therapeutically effective amount).
  • Dependent Claims: Narrow down the scope, adding specific features such as formulations with excipients, dosage forms, or specific patient populations.

For instance, if the patent claims a compound with a particular core structure substituted in a defined manner, it necessarily limits the scope but also offers strong defensibility against minor variations.

Scope Implications

  • Chemical Space: The scope covers the class of compounds sharing core structural motifs, which might provide flexibility for follow-on inventions.
  • Therapeutic Claims: If the patent claims treatment methods for specific indications, it can be a powerful tool to prevent generic competition in those markets.
  • Method of Use: Protective scope extends to subsequent patents on improvements or alternative methods of administration.

Legal and commercial strategic value hinges on how broad the independent claims are. Overly narrow claims risk easy workaround, while overly broad claims could face validity challenges if prior art exists.


Patent Landscape in Australia

Comparative Patent Activity

The patent landscape for similar therapeutics in Australia shows varied patenting activity, aligned with global trends:

  • Global Patent Filings: The patent family likely includes filings in major jurisdictions like the US, EP, JP, and China, with corresponding Australian filings to secure local rights.
  • Competitor Patents: Several patents possibly cover alternative compounds, formulations, or methods, contributing to a dense patent thicket around the same therapeutic area.
  • Patent Expiry and Lifecycle: Most pharmaceutical patents have an expiry date around 2030-2035, considering extensions like Supplementary Protection Certificates (SPCs) or patent term extensions.

Innovation Trends

The landscape reveals ongoing innovation in:

  • Novel heterocyclic compounds.
  • Improved bioavailability through formulation patents.
  • Combination therapies integrating the patented compound.
  • Biomarker-driven personalized medicine approaches.

Legal Considerations

Australian patent law emphasizes inventive step, novelty, and sufficiently disclosed claims. The presence of prior art challenges or obviousness arguments could influence the patent’s enforceability, especially in the realm of chemical and pharmaceutical patents.


Potential Challenges

  • Prior Art and Obviousness: Similar compounds disclosed in earlier patents or scientific literature might challenge the innovative step.
  • Claim Construction: Narrow claims may hinder enforcement, whereas broad claims are scrutinized for inventive merit.
  • Patent Term and Life Cycle: Approaching expiry could affect commercialization strategies.

Strategic Implications

In the context of the Australian market, AU2014329421’s scope provides:

  • Market Exclusivity: The patent’s claims defend against generic competition for the duration of the patent term.
  • Patent Enforcement: Clear claim boundaries facilitate enforcement actions against infringing entities.
  • Licensing Opportunities: Broad claims surrounding compound classes and therapeutic applications enhance licensing potential.

Successfully leveraging patent protection depends on maintaining novel claim scope, vigilant monitoring of the patent landscape, and rapid adaptation to emerging competitors.


Key Takeaways

  • The scope of AU2014329421 predominantly covers specific chemical compounds and their uses, with strategic implications for therapeutic exclusivity.
  • Claims crafted with optimal breadth balance enforceability with scope; overly broad claims risk validity challenges, whereas narrow claims limit protection.
  • The Australian patent landscape for similar therapeutics is dynamic, with active innovation, making due diligence essential.
  • Understanding claim boundaries and patent landscape intricacies informs R&D, licensing negotiations, and litigation strategy.
  • Continuous monitoring of patent lifecycle status and potential third-party patents is crucial for sustained market competitiveness.

FAQs

1. What determines the strength of the patent claims in AU2014329421?
The strength depends on claim breadth, specificity, novelty, and non-obviousness, balanced to maximize protection without risking invalidity under prior art.

2. How does Australian patent law impact the enforceability of pharmaceutical patents?
Australian law emphasizes inventive step, novelty, and sufficient disclosure. Validity challenges often arise based on prior art or claim construction issues.

3. Can modifications to the compound or formulation bypass the patent?
Potentially, if the modifications are sufficiently distinct and non-obvious, but close scrutiny of the patent claims and scope is necessary to assess infringement risks.

4. How does the patent landscape influence innovation strategies?
A dense patent landscape necessitates strategic patent filings, potential licensing, or collaboration, emphasizing the importance of continuous patent monitoring.

5. When will AU2014329421 likely expire, and what does this mean for market exclusivity?
Typical pharmaceutical patents in Australia last 20 years from filing; extensions via SPCs can add additional protection. Market exclusivity ends upon expiration, enabling generics.


References

[1] Australian Patent AU2014329421 full specification.
[2] Australian Patent Office guidelines.
[3] International patent filings related to the same therapeutic class.
[4] Patent landscape reports for pharmaceutical patents in Australia and globally.
[5] Australian patent law and court precedents.

Note: Specific legal events, dates, and detailed claim language require direct consultation of the patent document.

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