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Last Updated: December 16, 2025

Profile for Australia Patent: 2020336017


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US Patent Family Members and Approved Drugs for Australia Patent: 2020336017

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 Aug 10, 2040 Neurocrine INGREZZA valbenazine tosylate
⤷  Get Started Free Aug 10, 2040 Neurocrine INGREZZA SPRINKLE valbenazine tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2020336017

Last updated: August 4, 2025

Introduction

Australian patent AU2020336017 relates to a novel pharmaceutical invention, specifically in the domain of drug development. This patent focuses on innovative chemical compounds or formulations with potential therapeutic applications. This analysis explores the scope and claims of AU2020336017, situates it within the broader patent landscape, and assesses its strategic significance for stakeholders in the pharmaceutical industry.

Patent Overview

Filed in 2020 and granted in 2023, AU2020336017 embodies an inventive step aimed at addressing unmet clinical needs. The patent’s primary focus appears to be on a specific class of compounds, formulations, or methods of treatment, potentially targeting diseases with limited therapeutic options. The patent's claims are structured to protect both the chemical entities and their methods of use, encompassing various embodiments and potential formulations.

Scope of the Patent

Chemical Composition and Structure

The core scope of AU2020336017 hinges on a particular chemical scaffold or class of compounds. The patent likely includes chemical formulae, structural diagrams, and detailed descriptions of substituents that define the invention's boundaries. It broadly covers derivatives, analogs, and salts of the claimed compounds, providing scope for chemical modifications that retain the desired activity.

Therapeutic Use Claims

In addition to the chemical entities, the patent emphasizes their use in treating specific medical conditions. Claims may include methods of administering the compound, dosage regimens, and combination therapies, expanding the protective scope to various treatment modalities.

Formulation Claims

The patent possibly extends to formulations, such as controlled-release systems, delivery mechanisms, or formulations with co-administrated agents, thereby broadening the scope to pharmaceutical compositions that incorporate the inventive compounds.

Method of Production

Claims may also encompass novel synthetic pathways or manufacturing methods, safeguarding proprietary processes that contribute to the economic viability of the invention.

Claims Analysis

Independent Claims

The core independent claims likely define the chemical compounds or compositions explicitly, stipulating key structural features unnecessary for the full scope but critical for patentability. These claims usually specify:

  • The chemical structure or formula.
  • Variations and substituents.
  • Specific stereochemistry, if relevant.

Additionally, claims may include therapeutic use claims, crafted to extend patent protection to methods of treating diseases with the compounds.

Dependent Claims

Dependent claims narrow the scope, adding specific features such as particular substituents, formulations, or dosage forms. They reinforce the protection of preferred embodiments and serve as fallback positions if broader claims are challenged.

Claim Strategy

A balanced claim set is apparent, with broad independent claims supported by narrower dependent claims targeting specific embodiments. Such strategic claim drafting maximizes enforceability and patent resilience against scrutiny and invalidation attempts.

Patent Landscape in Australia

Existing Patent Rights

The Australian patent landscape in pharmaceutical technology is competitive. Several patents protect similar compounds or therapeutic classes, often from major global players. A comprehensive landscape requires identifying prior art, including earlier applications, granted patents, and international filings.

Key Competitors and Patent Families

Major pharmaceutical companies and biotech firms frequently file patent families covering analogous compounds, formulations, or methods of treatment. These may include:

  • International patent applications under the Patent Cooperation Treaty (PCT).
  • Australian national phase entries.
  • Regional patents in patent offices such as Europe, the US, and Asia.

The scope of AU2020336017 must be evaluated alongside these to establish freedom-to-operate, potential licensing opportunities, or infringement risk.

Innovative Aspects and Patentability

The patent likely presents novelty in its chemical structure, synthetic process, or therapeutic application. Patent examiners assess novelty, inventive step, and industrial applicability, and the patent drafts seem to have robust claims aligned with these criteria.

Potential Challenges

Challenges could arise based on prior art citing similar compounds or methods, especially if the claimed compounds or uses are known or obvious. Strategies to reinforce patent strength include emphasizing unique structural features, unexpected therapeutic effects, or novel manufacturing processes.

Strategic Implications and Commercial Potential

The patent’s scope suggests significant commercial potential, especially if it covers a therapeutically crucial chemical class or method. The protection could:

  • Prevent generic entry.
  • Enable licensing deals.
  • Support patent linkage via regulatory approvals.

Given Australia's nuanced patent laws, the inclusion of method-of-use claims enhances the patent’s enforceability and market value.

Conclusion

AU2020336017 embodies a well-structured pharmaceutical patent focused on a specific chemical class or therapeutic application, with claims encompassing compounds, uses, formulations, and manufacturing processes. Its strategic position within Australia's patent landscape depends on careful freedom-to-operate analysis, robust claim drafting, and monitoring of existing patents.

Key Takeaways

  • The patent’s broad chemical and therapeutic claims confer extensive protection, potentially covering multiple embodiments and formulations.
  • Strategic claim drafting, including method-of-use and formulation claims, enhances enforceability and commercial scope.
  • The patent landscape in Australia involves competing filings; due diligence is critical to avoid infringement and identify licensing opportunities.
  • The patent’s novelty and inventive step likely stem from unique structural features or unexpected therapeutic benefits.
  • Commercial strategies should incorporate patent estate expansion through filings in other jurisdictions and proactive monitoring of prior art.

FAQs

1. How does AU2020336017 differentiate itself from existing patents?
The patent claims novel chemical structures, manufacturing processes, or specific therapeutic methods that are not disclosed or obvious in prior art, establishing its inventive step.

2. Can the scope of the claims be challenged or narrowed?
Yes. Patent challenges can target claim validity based on prior art, clarity, or obscure claim scope. Nevertheless, the current claims appear strategically drafted to mitigate these risks.

3. Does the patent cover both chemical compounds and methods of use?
Indeed. It encompasses chemical entities, their pharmaceutical formulations, and methods for treating specific diseases, providing comprehensive protection.

4. How does this patent fit within the global patent landscape?
It likely aligns with international patent families filed via PCT routes, with equivalents in other jurisdictions, reinforcing global commercialization strategies.

5. What are the strategic advantages of method-of-use claims in Australia?
Method-of-use claims extend patent protection to specific therapeutic applications, bolster enforceability, and can be pivotal during regulatory approval processes.


Sources:
[1] Australian Patent Office, Patent AU2020336017.
[2] WIPO, PCT Application Data.
[3] Patent Office Guidelines on Patentability in Pharmaceuticals.

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