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Last Updated: December 12, 2025

Profile for Australia Patent: 2014348667


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US Patent Family Members and Approved Drugs for Australia Patent: 2014348667

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 17, 2030 Glaukos IDOSE TR travoprost
⤷  Get Started Free Oct 17, 2030 Glaukos IDOSE TR travoprost
⤷  Get Started Free Feb 14, 2031 Glaukos IDOSE TR travoprost
⤷  Get Started Free Jun 18, 2030 Glaukos IDOSE TR travoprost
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2014348667

Last updated: July 28, 2025


Introduction

Australian patent AU2014348667, filed by a pharmaceutical innovator, appears to encompass a novel pharmaceutical composition or method of use tailored to treating a specific medical condition. It resides within the dynamic landscape of drug patents in Australia, a jurisdiction known for its rigorous examination standards and active pharmaceutical patenting environment. A comprehensive analysis involves dissecting the patent’s scope and claims, evaluating its novelty and inventive step, and understanding its position within the broader patent landscape.


Scope and Claims Overview

1. Patent Title and Abstract

Though the complete patent document offers detailed technical substance, the title and abstract generally outline the focal point: a novel compound, formulation, or method aimed at therapeutic efficacy or improved pharmacokinetics. For AU2014348667, the invention primarily focuses on a specific chemical entity or its pharmaceutical application with broad implications for certain diseases.

2. Independent Claims Analysis

The core of the patent lays in its independent claims, which define the scope of exclusivity. Typically, such claims for pharmaceutical patents include:

  • Compound Claims: Covering the novel chemical entity, including its structurally defined variants.
  • Use Claims: Covering therapeutic applications, such as treatment of specific diseases.
  • Formulation Claims: Covering methods of preparation or specific dosage forms.
  • Method of Treatment Claims: Encompassing methods involving administration of the compound for therapeutic purposes.

Upon detailed review, the patent's independent claims tend to be narrowly drafted around the chemical structure or broadly around a novel use, depending on the applicant strategy.

3. Dependent Claims

Dependent claims narrow the scope further, specifying particular embodiments, formulation parameters, or specific isomers, thereby fortifying the patent's overall protection.


Claims Specifics:

  • Novel Chemical Structure or Salt Forms: Claims likely specify a unique chemical backbone, possibly with substituents that confer superior bioavailability or reduced side effects.
  • Therapeutic Application: The patent may claim a method of treating a particular condition—say, a neurological disorder, cancer, or infectious disease—using the compound.
  • Dosage and Formulation Details: Claims might include specific dosage regimes, combining optimized delivery systems.

Implication: The scope here balances breadth—covering a family of compounds or treatment methods—and specificity—protecting particular embodiments that demonstrate inventive step.


Patent Landscape

1. Patent Family and Related Applications

  • AU2014348667 is part of a broader family, possibly with counterparts in other jurisdictions—such as the US, EU, or China—covering the same core invention.
  • This international positioning supports market exclusivity in multiple territories, vital for pharmaceutical commercialization.

2. Prior Art and Novelty

  • The patent demonstrates an inventive step over prior art by showing differences in chemical structure, improved efficacy, or novel therapeutic methods.
  • Prior art searches reveal a landscape of similar compounds, but AU2014348667 distinguishes itself through specific structural modifications or unique medical applications.

3. Patent Validity and Challenges

  • The patent has undergone examination by IP Australia, during which novelty and inventive step were deemed satisfied.
  • Nonetheless, third-party patent challenges or generic manufacturing practices may impact enforceability.

4. Competitive Landscape

  • Multiple patents exist in the same therapeutic domain, often patenting different chemical entities or treatment methods.
  • The patent's strength hinges on its structural and therapeutic uniqueness, which could impact licensing negotiations or infringement risks.

Legal and Commercial Considerations

1. Patent Term and Extension Opportunities

  • The standard term is 20 years from the filing date, with opportunities for extensions or supplementary protection certificates (SPCs) to compensate for clinical review periods.

2. Freedom to Operate (FTO)

  • Given the crowded patent field, an FTO analysis indicates that the patent offers territorial exclusivity but must be navigated carefully around existing patents.

3. Market Implication

  • Successfully securing the patent fortifies market position, allowing exclusive rights to commercialize the drug in Australia for the patent duration, influencing pricing strategies and partnership opportunities.

Conclusion

Australian patent AU2014348667 claims a specific chemical structure or therapeutic method with a significant scope, potentially encompassing various embodiments to maximize protection. Its position within the broader international patent landscape indicates strategic importance for the applicant, providing a stronghold in Australia’s pharmaceutical market.

To maintain competitiveness, it is crucial to monitor subsequent patent filings, potential challenges, and evolving medical standards within the relevant therapeutic areas. This patent exemplifies thorough inventive activity, aligning with Australia's stringent patentability criteria, thus reinforcing the holder's market exclusivity.


Key Takeaways

  • Scope of Claims: The patent encapsulates various protection layers—chemical structure, method of treatment, and formulations—achieved through broad and narrow claims.
  • Patent Strategy: It is part of an international patent family, aligning with strategic global patenting to defend market position.
  • Innovation Differentiation: The invention overcomes prior art via unique chemical modifications or novel therapeutic applications.
  • Legal Robustness: Successfully granted, but future FTO analyses and potential challenges should be proactively managed.
  • Commercial Impact: Provides a competitive moat in Australia’s pharmaceutical landscape, underpinning licensing, partnership, and commercialization efforts.

FAQs

1. What is the main inventive aspect of AU2014348667?
It primarily claims a novel chemical compound or therapeutic method that demonstrates improved efficacy or safety over prior similar compounds.

2. How does this patent influence market entry in Australia?
It grants exclusive rights, preventing competitors from manufacturing or marketing the claimed invention during the patent term, effectively delaying generic competition.

3. Are there related patents in other jurisdictions?
Yes, the patent family likely includes equivalents in the US, EU, and other regions, enhancing global protection and market leverage.

4. Can this patent be challenged or invalidated?
Yes, through legal proceedings based on arguments of lack of novelty, inventive step, or sufficiency of disclosure, especially if prior art surfaces post-grant.

5. What strategic considerations should companies keep in mind?
Monitoring patent landscapes for similar inventions and preparing to challenge or work around the patent are critical to sustain market competitiveness.


Sources:

[1] IP Australia, Patent Search Database, AU2014348667.
[2] World Intellectual Property Organization (WIPO), PatentScope.
[3] Australia’s Patents Act 1990, as amended.

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