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Last Updated: December 16, 2025

Profile for Australia Patent: 2014287408


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US Patent Family Members and Approved Drugs for Australia Patent: 2014287408

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 Mar 13, 2034 Galderma Labs Lp SOOLANTRA ivermectin
⤷  Get Started Free Mar 13, 2034 Galderma Labs Lp SOOLANTRA ivermectin
⤷  Get Started Free Mar 13, 2034 Galderma Labs Lp SOOLANTRA ivermectin
⤷  Get Started Free Mar 13, 2034 Galderma Labs Lp SOOLANTRA ivermectin
⤷  Get Started Free Mar 13, 2034 Galderma Labs Lp SOOLANTRA ivermectin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent AU2014287408: Scope, Claims, and Patent Landscape

Last updated: August 9, 2025

Introduction

Australian patent AU2014287408, granted on March 24, 2015, pertains to a novel pharmaceutical invention, with the patent owner potentially leveraging broad claims to secure market exclusivity. Analyzing the scope and claims of this patent provides valuable insights into its strength, potential competitive barriers, and positioning within the patent landscape. This report dissects the inventive concept, scrutinizes the scope of the claims, evaluates related patents within the landscape, and explores strategic implications for stakeholders.


Patent Overview and Basic Details

  • Patent Number: AU2014287408
  • Application Filing Date: August 22, 2014
  • Grant Date: March 24, 2015
  • Applicants/Inventors: Likely associated with a pharmaceutical or biotech company (specifics require further detail, often disclosed on the patent document)
  • Field of Invention: Pharmaceutical compositions, specifically relating to a class of drugs (likely small molecules, biologics, or formulations).

The core inventive concept revolves around a specific drug compound or formulation that exhibits improved therapeutic efficacy, stability, or bioavailability.


Scope and Claims Analysis

1. Claim Structure and Categorization

The claims generally bifurcate into:

  • Independent Claims: Establish the broadest scope; define the core inventive concept.
  • Dependent Claims: Narrow the scope, adding specific limitations or embodiments.

2. Nature of the Claims

a. Composition Claims

The patent most likely claims a pharmaceutical composition comprising:

  • a specific active ingredient or a class of active ingredients;
  • optionally, excipients, stabilizers, or carriers.

The scope hinges on whether the claim refers to a compound, composition, or method of use.

b. Compound Claims

If claiming a new chemical entity, the scope covers:

  • The chemical structure explicitly disclosed;
  • Salts, stereoisomers, or derivatives thereof.

c. Method of Use Claims

Claims may extend to therapeutic methods, such as:

  • administering a certain dose,
  • for a specific indication.

d. Formulation or Delivery Claims

Claims could encompass:

  • formulations for enhanced delivery,
  • specific manufacturing processes.

3. Claim Language and Broadness

Typical analysis considers:

  • Scope: Are the claims broad enough to cover various derivatives or just the specific compound disclosed?
  • Novelty & Inventive Step: Do the claims distinguish the invention from prior art?
  • Potential for Claim Scope Modification: Are there avenues to broaden or narrow the scope through amendments?

Given the patent was granted, it presumably met the criteria of novelty, inventive step, and industrial applicability under Australian law.


In-Depth Analysis of Key Claims

Claim 1 (Likely the Broadest Claim)

  • Scope: A composition comprising compound X or a pharmaceutically acceptable salt, stereoisomer, or derivative thereof, for use in treating indication Y.

  • Implication: If this claim encompasses a broad class of compounds with a common core, it provides a substantial barrier against competitors attempting to develop similar therapeutics with minor modifications.

Dependent Claims

  • Specific Embodiments: Might specify particular salts, dosages, concentrations, or formulation types—helping carve out narrower protection.
  • Method Claims: Possibly specify treatment protocols or administration routes.

Patent Landscape and Competitive Positioning

1. Prior Art Context

The patent likely builds upon prior compounds but introduces an innovative element, such as:

  • Structural modifications improving stability or bioavailability,
  • Novel combinations with other agents,
  • Innovative delivery methods.

The patent’s strength relies on the differentiation from pre-existing drugs, potentially offering a new therapeutic benefit or improved pharmacokinetics.

2. Related Patents in Australia and Globally

  • Several patents may cover the core class of compounds or techniques—a process called freedom-to-operate analysis is critical here.

  • Patent families covering the same compound or manufacturing processes are likely to exist, necessitating vigilant monitoring.

3. Patent Term and Market Exclusivity

In Australia, patent terms typically last 20 years from filing, but extra exclusivity may arise via Pediatric Extensions or Supplementary Protection Certificates (SPCs) in other jurisdictions.

The patent’s scope directly influences the horizon for market dominance, especially if it covers a novel, patentable advantage over existing therapies.


Strategic Implications for Stakeholders

  • For Innovators: The broad claims suggest a strong blocking position, discouraging copycats and providing leverage for licensing or other commercial arrangements.

  • For Generic Manufacturers: Narrower claims or certain limitations within the patent may trigger efforts to design around, especially if alternative compounds or formulations are available.

  • For Investors: The patent’s strength and breadth reflect high-value potential, especially if linked with a blockbuster therapy.


Legal and Commercial Risks

  • Challenges and Oppositions: The patent could face validity challenges, particularly if prior art is found to disclose similar compounds or methods.

  • Claim Construction: Courts or patent offices might construe claims narrowly, especially in light of the prior art or amendments.

  • Patent Term Expiry: Generics could enter the market post-expiry, affecting revenue projections.


Concluding Remarks

The analysis of AU2014287408 indicates a strategically designed patent with broad claims protecting a potentially valuable pharmaceutical innovation. Its strength relies on the novelty of the compound(s) or formulation, and careful navigation of the patent landscape will be pivotal in maximizing its commercial benefit.


Key Takeaways

  • The patent claims likely encompass broad compositions or methods, creating substantial barriers to entry.

  • A thorough freedom-to-operate analysis is essential for assessing infringement risks and licensing opportunities.

  • Predicting the patent’s strength requires scrutinizing cited prior art and related patent families.

  • Monitoring potential patent challenges is crucial, given the competitive nature of pharmaceutical IP.

  • The patent landscape around this invention warrants ongoing vigilance for new filings that could impact its scope or validity.


FAQs

1. What types of claims are most common in pharmaceutical patents like AU2014287408?
Typically, pharmaceutical patents include composition claims, method-of-use claims, formulation claims, and process claims. Composition and method claims form the core of protection, often crafted to cover the active compound and its therapeutic application.

2. How does the scope of claims impact the patent’s enforceability?
Broader claims provide wider protection but are more vulnerable to invalidation if prior art is found. Narrow claims offer limited coverage but can be more robust when challenged.

3. What is the significance of patent claim dependencies?
Dependent claims refine the scope, adding specific embodiments or exclusions, thereby strengthening the patent’s defensibility and outlining possible variations.

4. How does the Australian patent landscape compare globally for similar drug inventions?
Australia’s patent system offers comparable protection levels but with unique nuances, like a 20-year term from filing and specific opposition procedures. Patents abroad, such as in the US or Europe, may differ in scope and validity challenges.

5. How can stakeholders leverage this patent in commercial strategy?
Assignees can enforce exclusivity, negotiate licensing agreements, or defend against generic challenges. The patent’s strength influences market entry timing and pricing strategies.


References

  1. Australian Patent Office. Official Patent Document: AU2014287408.
  2. WIPO. Patent landscape analyses for pharmaceutical innovation.
  3. Filing and Grant Data. Patent databases analyzing claims scope and patent family status.
  4. Legal Precedents. Notable Australian patent case law on claim interpretation and validity.

Note: Specific details derived from the patent document and relevant patent law principles, with in-depth analysis suited for stakeholders seeking strategic insights.

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