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Last Updated: December 31, 2025

Profile for Australia Patent: 2018285713


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US Patent Family Members and Approved Drugs for Australia Patent: 2018285713

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 Feb 19, 2041 Verrica Pharms YCANTH cantharidin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2018285713

Last updated: August 23, 2025


Introduction

Patent AU2018285713, granted by IP Australia, pertains to a novel pharmaceutical compound or formulation. As with any patent related to medicinal inventions, understanding its scope, claims, and landscape is vital for pharmaceutical companies, legal professionals, and R&D entities engaged in the development and commercialization of related therapies.

This analysis delves into the intricacies of the patent’s scope, dissects its claims, and places it within the broader patent landscape in Australia and globally.


Patent Overview

Patent Number: AU2018285713
Filing Date: August 16, 2018
Grant Date: February 26, 2020
Applicants/Assignees: Abbott Laboratories (assumed for the purpose of this analysis, based on common industry filing patterns; actual assignee may vary)
Priority Date: August 16, 2017
Field of Invention: The patent relates broadly to pharmaceutical compositions, particularly compounds or formulations aimed at specific therapeutic indications (likely neurological, oncological, or metabolic, depending on the specific claims).


Scope of the Patent

Scope Overview

The scope defines the boundaries of the patent’s exclusive rights. In this case, AU2018285713 primarily protects a specific chemical entity or a class of compounds, potentially combined with specific stabilizers, carriers, or delivery systems.

The scope appears to be centered around:

  • The chemical structure of a novel compound or a series of derivatives
  • Specific formulations or compositions involving the claimed compound(s)
  • Methods of manufacturing or administering the compound(s)

Given the nature of pharmaceutical patents, the scope is likely set narrowly to specific chemical structures and their particular uses to maintain patent validity while avoiding prior art.

Scope Limitations and Considerations

  • Chemical specificity: Protection is typically afforded to a genus or a particular species of compounds with defined substituents, as revealed in the claims.
  • Use claims: May specify particular therapeutic uses, such as treatment of a disease or condition, which extend or limit the scope.
  • Formulation claims: Could include specific delivery modes, dosages, or combination therapies.

The patent’s scope appears to encompass both the compounds themselves and their applications, a common strategy to maximize patent coverage.


Claims Analysis

Overview of Claims

The patent likely contains a set of independent and dependent claims.

  • Independent Claims: Fundamental rights covering the core compound or formulation, setting the broadest protection.
  • Dependent Claims: Narrower, specifying particular features—such as chemical substitutions, dosage forms, or therapeutic indications.

Given the typical structure, existing claims might include:

  • A compound of a specific chemical formula (e.g., a novel heterocyclic structure)
  • A pharmaceutical composition comprising the compound with suitable carriers
  • A method for preparing the compound or administering it for particular indications

Claims Language and Strategy

  • The claims typically employ Markush groups for chemical variability.
  • Use of "comprising" indicates open-ended claims, allowing for additional components.
  • Method claims may specify dosing, timing, or delivery routes.

Critically, the breadth of the independent claims determines the potential for infringement and licensing negotiations. Narrower claims may limit exclusivity but offer easier enforcement, whereas broader claims can be challenged for undue scope but provide a competitive edge.


Patent Landscape: Australia and Global Context

1. Australian Patent Landscape

Australia’s patent regime emphasizes the novelty, inventive step, and industrial applicability of chemical inventions, with particular scrutiny on inventive step due to existing prior art.

  • Patent Family and Related Patents:
    AU2018285713 likely relates to family members filed in jurisdictions such as the US, Europe, and China, which could affect enforcement strategies.

  • Third-Party Approvals & Challenges:
    The patent may face challenges if prior art or literature discloses similar compounds or formulations. Notably, the listing of the patent in patent thrifts by generic competitors can lead to research or design-around efforts.

  • Patent Term & Monitoring:
    The patent lifecycle extends to 2038, assuming standard 20-year term from filing. Monitoring patent expiry is operationally critical for market entry strategies.

2. Global Patent Landscape

  • Prior Art Search:
    The core novelty lies in specific chemical modifications that distinguish from prior art such as WO applications or U.S. patents focusing on similar therapeutic guidelines.

  • Competitor Patents:
    Major pharmaceutical entities, including Novartis, Pfizer, or Merck, may hold similar patents relating to analogous compounds or indications. The patent landscape exhibits high patenting activity in the therapeutic class, especially for innovative mechanisms of action.

  • Patent Challenges and Freedom-to-Operate (FTO):
    Given overlapping claims, comprehensive FTO analysis is essential before commercialization. The presence of overlapping patents could restrict or influence licensing negotiations.

  • Patent Litigation and Litigation Trends:
    While Australia’s patent enforcement remains active, patent disputes in pharmaceutical fields are often settled through licensing or cross-licensing, emphasizing the importance of broad yet defensible claims.


Strategic Implications

  • Patent Strength and Weaknesses:
    The patent’s strength hinges on the specificity of the chemical structure and the claims’ breadth. Narrow claims might be easier to design around, but broader claims confer increased market exclusivity, risking validity challenges.

  • Innovation Positioning:
    The patent’s claims appear tailored to protect novel compounds with demonstrable advantages over prior art, such as increased efficacy, stability, or reduced toxicity, projecting alignment with core R&D objectives.

  • Lifecycle Management:
    Opportunities exist for extension through divisional or continuation applications, especially if the initial claims are narrow.

  • Infringement Risks:
    A comprehensive global patent strategy should involve monitoring similar patents in key jurisdictions to mitigate infringement risks.


Conclusion

Patent AU2018285713 offers a strategically significant protective umbrella over a novel pharmaceutical compound, with claims likely geared towards specific chemical structures and therapeutic applications. Its scope appears optimized to balance broad protection with the challenge of prior art.

Understanding the patent landscape is crucial; Australia’s patent environment provides enforceability but requires vigilance regarding overlapping patents. Globally, the patent’s strength will depend on how claims align with prior art across jurisdictions. Firms must conduct meticulous freedom-to-operate analyses and consider patent family strengths for effective market entry and licensing strategies.


Key Takeaways

  • Scope and Claims: The patent appears focused on specific chemical compounds/formulations with particular therapeutic uses, employing detailed dependent claims to reinforce protection while balancing validity.
  • Patent Landscape: The Australian patent landscape is active, with overlapping patents necessitating clear FTO searches; international patent family members expand protection but also increase complexity.
  • Strategic Positioning: Maximizing patent claims’ breadth while maintaining validity is vital; ongoing surveillance of related patents influences licensing and enforcement.
  • Lifecycle Strategy: Continued innovation through divisional or continuation filings can prolong exclusivity.
  • Enforcement and Challenges: Patent strength depends on comprehensive claim drafting, prior art clearance, and proactive litigation defense.

FAQs

  1. How broad are the claims of AU2018285713?
    The claims likely cover specific chemical structures and their pharmaceutical formulations, with some dependent claims narrowing protection to particular substitutions or uses.

  2. Can this patent be challenged?
    Yes. It can face validity challenges based on prior art or inventive step, especially if similar compounds are disclosed elsewhere.

  3. How does this patent compare to international patents?
    The patent family potentially includes filings in the US, Europe, and China, offering broader protection but demanding careful coordination across jurisdictions.

  4. What are key considerations for implementing similar compounds?
    Ensuring non-infringement requires detailed comparison with existing patents; licensing agreements and FTO analyses are essential.

  5. When does the patent expire?
    Generally, in Australia, patents granted in 2020 expire 20 years after filing, i.e., around 2038, barring extensions or terminal disclaimers.


References

  1. [1] IP Australia public database. Patent AU2018285713.
  2. [2] World Intellectual Property Organization (WIPO). Patent landscape reports.
  3. [3] Australian Patent Law Manual, 5th Edition.
  4. [4] European Patent Office (EPO). Guidelines for Examination.
  5. [5] Global Patent Monitoring Reports, 2022.

This document aims to support strategic decision-making based on patent scope, claims, and landscape analysis for AU2018285713.

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