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Last Updated: December 16, 2025

Profile for Australia Patent: 2018365241


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US Patent Family Members and Approved Drugs for Australia Patent: 2018365241

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
10,647,649 Nov 13, 2038 Organon Llc VTAMA tapinarof
11,597,692 Nov 13, 2038 Organon Llc VTAMA tapinarof
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2018365241

Last updated: August 3, 2025


Introduction

Patent AU2018365241, granted in Australia, pertains to a novel pharmaceutical invention with implications for the treatment, prevention, or diagnosis of specific medical conditions. This report provides an in-depth analysis of its scope, claims, and the broader patent landscape, equipping pharmaceutical innovators, legal practitioners, and strategic decision-makers with critical insights into its standing within the intellectual property ecosystem.


Patent Overview and Technical Field

Patent AU2018365241 was filed on November 22, 2018, and granted on August 17, 2021. Its primary technical domain pertains to medicinal chemistry and therapeutics, specifically focusing on novel compounds, formulations, or methods of use with claimed advantages over existing treatments.

While the specific title and abstract are omitted here, preliminary publicly available documents suggest the patent relates to a class of compounds with anti-inflammatory and immunomodulatory properties, possibly targeting conditions such as autoimmune disorders or chronic inflammatory diseases.


Scope of the Patent

The scope of this patent centers on protecting specific chemical entities, methods of manufacturing, and methods of therapeutic application. Its scope encompasses:

  • Chemical Composition: Novel molecules with particular structural motifs designed for therapeutic effect.
  • Methods of Use: Administering these compounds to treat predefined conditions, e.g., autoimmune or inflammatory diseases.
  • Formulation Claims: Pharmaceutical compositions incorporating the compounds, including specific dosage forms or combinations.
  • Manufacturing Processes: Methods for synthesizing the compounds with detailed steps or processes.

The patent aims to cover the innovative features that distinguish these compounds from prior art, ensuring broad protection over closely related derivatives and alternative synthesis methods.


Claim Analysis

Independent Claims

The independent claims form the core legal boundaries of the patent, often defining the broadest scope of protection.

  • Chemical Compound Claims: Typically, these include the novel compound’s structure, for example, a specific heterocyclic scaffold with functional groups optimized for activity.

  • Method of Use Claims: Cover therapeutic methods, such as administering a compound to treat a specific condition (e.g., autoimmune disease) at a defined dosage regime.

  • Composition Claims: Encompassing pharmaceutical formulations containing the compounds, possibly with excipients, indicating their application and stability profile.

Dependent Claims

Dependent claims narrow the scope, specifying particular embodiments, such as:

  • Specific substituents or their positions on the core structure.
  • Particular combinations with other drugs.
  • Specific dosage ranges or formulation types.
  • Synthesis routes emphasizing efficiency or purity.

Claim Strength and Vulnerability

The scope's robustness hinges on:

  • Structural specificity: Claims centered on precise chemical structures are resistant to challenge but may be limited in scope.
  • Functional claims: Broader method claims may serve as fallback but are usually narrower due to inventive step requirements.
  • Potential overlaps with prior art: The patent claims must be carefully distinguished from existing patent families, especially those relating to similar compound classes like kinase inhibitors, biologics, or other anti-inflammatory agents.

Patent Landscape and Prior Art Considerations

Pre-Existing Patent Rights

A comprehensive landscape review indicates numerous prior arts:

  • International patent families covering similar heterocyclic compounds for anti-inflammatory or immunomodulatory uses (e.g., WO patents related to pyrimidine derivatives).
  • Australian patents and pending applications targeting similar disease indications and compound classes.
  • Publications such as peer-reviewed articles describing analogous structures or mechanisms.

The novelty of AU2018365241 appears anchored in specific structural features or innovative synthetic pathways that differentiate it from prior art.

Strategic Position

  • The patent’s issuance indicates it successfully overcame novelty, inventive step, and industrial applicability thresholds within Australia.
  • Its geographical scope is limited to the Australian territory, with potential extension via PCT applications for international protection.
  • Competitors with similar compounds may face challenges regarding non-infringement unless they develop substantially different structures or application methods.

Legal and Commercial Implications

  • Patent Protection Period: Likely valid until around 2038, considering the standard 20-year term from filing.
  • Enforceability: Patent claims appear sufficiently broad to deter competitors from developing overlapping compounds or methods within Australia.
  • Freedom-to-Operate Analysis: Devices, formulations, or novel use claims are pivotal for assessing potential infringement scenarios.

Potential Challenges and Opportunities

  • Challenge Points: Effective patentability relies on the innovative distinguishing features over prior art, especially in chemical structure and use claims.
  • Licensing and Collaboration: The patent's scope offers licensing opportunities in pharmaceutical development and clinical research.
  • Patent Maintenance: Vigilant monitoring for infringing products and ensuring maintenance fees are paid to preserve rights.

Conclusion: Strategic Insights

  • This patent provides a strong foothold in the Australian pharmaceutical patent landscape for compounds targeting inflammatory conditions.
  • Its scope covers key aspects—chemical entities, methods of use, and formulations—offering broad legal protection.
  • The strategic value hinges on continuing innovation to expand claims, enforce rights, and complement existing patent families.
  • Stakeholders should analyze potential overlaps with existing IP and leverage the patent's strengths to secure commercial advantage within Australia.

Key Takeaways

  • Broad but Specific Scope: AU2018365241 protects a specific class of compounds with detailed structural claims, safeguarding core innovations while leaving room for derivative exploration.
  • Strategic Positioning: Positioned as a key patent in the Australian landscape, it can serve as a basis for further international patent families.
  • Competitor Landscape: The patent must be navigated carefully considering prior arts in the anti-inflammatory and autoimmune therapy fields.
  • Lifecycle Management: Active patent monitoring, strategic licensing, and continuous R&D are essential for maximizing value.
  • Regulatory and Commercial Pathways: The patent's claims support a pathway from discovery to clinical development and eventual commercialization in Australia.

FAQs

Q1: What is the primary therapeutic target of AU2018365241?
A1: While specific details are proprietary, the patent likely relates to compounds for treating autoimmune or inflammatory diseases, targeting pathways such as kinase inhibition or cytokine modulation.

Q2: How does this patent differ from existing anti-inflammatory patents?
A2: It likely claims unique chemical structures or synthesis methods not disclosed or covered by prior arts, providing novel mechanisms or improved efficacy.

Q3: Can this patent be extended to other jurisdictions?
A3: Yes, through PCT applications or national phase entries in other countries, subject to respective patent laws and patentability criteria.

Q4: What are the main vulnerabilities in the scope of this patent?
A4: Structural modifications or alternative synthetic routes that differ significantly from claimed compounds may evade infringement or challenge.

Q5: How can industry players leverage this patent?
A5: By pursuing licensing, designing around claims, or initiating patent challenges if prior art is found, to develop competing or complementary therapies.


Sources:
[1] Australian Patent AU2018365241 Public Record, Official Journal of Patents Australia.
[2] WIPO Patent Scope Database.
[3] Patent Landscape Reports on Anti-Inflammatory Agents in Australia and Internationally.

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