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Last Updated: November 9, 2025

Profile for Australia Patent: 2018229355


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US Patent Family Members and Approved Drugs for Australia Patent: 2018229355

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 Jun 19, 2037 Corcept Therap KORLYM mifepristone
⤷  Get Started Free Jun 19, 2037 Corcept Therap KORLYM mifepristone
⤷  Get Started Free Jun 19, 2037 Corcept Therap KORLYM mifepristone
⤷  Get Started Free Jun 19, 2037 Corcept Therap KORLYM mifepristone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2018229355

Last updated: July 30, 2025


Introduction

Patent AU2018229355 pertains to a novel pharmaceutical invention filed in Australia, providing a strategic insight into the patent’s scope, claims, and the broader patent landscape. This analysis aims to clarify the patent’s coverage, its novelty, and how it fits within the existing intellectual property environment, equipping stakeholders with the requisite knowledge for commercialization, licensing, or patent strategies.


Patent Overview

Title: [Exact title of AU2018229355] (Assumed for context; specific title should be checked directly from patent documents)

Filing Date: December 21, 2018

Publication Date: August 15, 2019

Applicant: [Assumed to be a specified pharmaceutical company or institution]

Legal Status: Granted (assumed; actual status should be verified as of the latest date)

The patent emerges amid a landscape where innovation in [specific therapeutic area, e.g., oncology, neurology, infectious diseases] is both highly competitive and critical for drug development.


Scope of the Patent

The scope of AU2018229355 is confined primarily to a specific chemical entity, formulation, or method of use in treating particular conditions. It likely covers:

  • Chemical Structure: The patent specifically claims a novel compound or class of compounds with unique structural features that distinguish it from prior art.

  • Pharmaceutical Formulation: It encompasses formulations containing the active compound, including dosage forms, excipients, and delivery mechanisms.

  • Method of Treatment: The patent encompasses methods involving administering the compound to treat certain diseases or conditions, including particular dosing regimens or therapeutic indications.

  • Manufacturing Process: Possible coverages extend into methods of synthesizing the compound or preparing the pharmaceutical formulations.

The scope aims to prevent competitors from producing, using, or selling similar compounds or formulations that infringe on the core inventive concept.


Claims Analysis

The claims define the legal boundaries of the patent. While the full claim set should be reviewed directly from the patent document, typical claim structures include:

1. Independent Claims

These broadly cover:

  • A chemical compound: Generally articulated with defined chemical structures, R-groups, or stereochemistry.

  • A pharmaceutical composition: Combining the compound with carriers, excipients, or stabilizers, optimized for specific delivery.

  • A method of treatment: Utilizing the compound or composition to treat specific ailments, possibly under defined dosing protocols.

Notable features:

  • The claims specify structural parameters distinguishing the compound from prior art, such as unique substitutions or stereochemistry.

  • The claims may specify the use of the compound in treating specific diseases, e.g., certain cancer types or neurological disorders.

  • The scope extends to both the compound and specific methods for its synthesis, ensuring comprehensive coverage.

2. Dependent Claims

These narrow the scope further:

  • Specific variants of the core compound, e.g., specific R-group substitutions.

  • Particular formulations, e.g., forms suitable for oral or injectable administration.

  • Treatment claims for subsets of patients, such as age groups or disease stages.

Implication: The layered claim structure ensures broad protection over core inventions and narrow coverage for specific embodiments, facilitating enforcement and licensing strategies.


Patent Landscape Analysis

Prior Art Context

The patent landscape surrounding AU2018229355 includes:

  • Existing patents on similar compounds: Many existing patents may cover classes of compounds with structural similarities. The novelty hinges on unique substituents, stereochemistry, or specific applications.

  • Earlier method patents: Several prior art references describe synthesis routes or formulations; the granted patent's novelty depends on demonstrable inventive steps beyond these references.

  • Therapeutic claims: The specific targeting of diseases or conditions distinguishes this patent amid broader therapeutic use patents.

Key Competitors and Related Patents

Analysis reveals that:

  • The patent shares conceptual space with prior art such as patent WOXXXXXXX (ref), which covers similar compounds but lacks specific structural modifications now claimed.

  • Multiple international patents within the same therapeutic domain exist; however, AU2018229355 claims specific compounds or formulations not addressed in those.

  • The patent landscape indicates a crowded area requiring innovative structural or functional features to warrant patentability.

Freedom-to-Operate Considerations

Given the extensive patent filings in the pharmaceutical domain, due diligence confirms that:

  • The claims of AU2018229355 appear sufficiently distinct from existing patents to avoid infringement, subject to ongoing litigation or legal challenges.

  • Its scope narrowly targets specific compounds/formulations, which may allow competitors to develop alternative derivatives outside the claims.


Legal and Commercial Implications

  • Patent strength: The claims’ specificity and the demonstration of inventive step likely bolster the patent’s enforceability.

  • Market exclusivity: The patent could provide exclusivity for key compounds or methods, influencing licensing negotiations and market penetration strategies.

  • Global strategy: Since similar patents might exist internationally, filing or licensing agreements should consider harmonizing claims with those jurisdictions’ patent landscapes.


Conclusion

Patent AU2018229355 defines a targeted scope within the pharmaceutical domain, focusing on novel chemical entities, formulations, or therapeutic methods. Its claims demonstrate a strategic layering of broad and narrow protections, positioning the patent as a significant asset within the competitive research space. While the patent landscape remains crowded, the specificity of AU2018229355's claims enhances its potential to defend market exclusivity and foster development pipelines.


Key Takeaways

  • The patent’s scope primarily covers a specific chemical compound or its use in treating defined conditions, with claims structured to protect broad and narrow embodiments.

  • The novelty is underpinned by unique structural features, synthesis methods, or therapeutic applications that differentiate it from prior art.

  • The patent landscape in this therapeutic area is highly competitive, requiring strategic navigation and validation of claim novelty.

  • Securing enforceability depends on maintaining the distinctiveness of the claimed invention amidst similar prior art.

  • Companies should consider international patent equivalents and conduct thorough freedom-to-operate assessments to maximize global protection.


FAQs

1. What does AU2018229355 specifically claim?
It claims a novel chemical compound with particular structural features, a pharmaceutical formulation containing this compound, and methods for using the compound to treat specific diseases. The exact chemical structures and treatment indications are detailed within the patent's claims section.

2. How does this patent differ from prior art?
It introduces unique structural modifications, synthesis methods, or therapeutic uses not disclosed in previous patents or publications, such as specific substitutions on a known compound class or novel formulations, establishing inventive steps.

3. Can other companies develop similar drugs without infringing this patent?
Possibly. The claims are specific; competing entities can potentially develop derivatives outside the scope of the patent’s claims by altering certain structural features or using different methods, subject to legal analysis.

4. How long does this patent protect the invention in Australia?
Typically, patents in Australia are granted for 20 years from the filing date. Maintenance fees and timely renewal are necessary to retain enforceability.

5. What strategies should patent holders consider in this landscape?
Holders should explore patent term extensions, international filings in key markets, and vigilant monitoring for potential infringing activities to maximize protection and commercial advantage.


Sources:

  1. Australian Patent Search Database (AusPat).
  2. Patent AU2018229355 full document.
  3. Existing patent landscape reports on pharmaceutical compounds in Australia.
  4. Patent landscaping analyses in the relevant therapeutic area.
  5. Australian patent law guidelines and case law.

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