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Last Updated: December 17, 2025

Profile for Australia Patent: 2018229817


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US Patent Family Members and Approved Drugs for Australia Patent: 2018229817

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
11,168,058 Feb 27, 2038 Bayer Healthcare NUBEQA darolutamide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2018229817

Last updated: August 3, 2025

Introduction

Australian Patent AU2018229817, titled "Novel pharmaceutical compounds and compositions", pertains to a patent application filed in Australia, reflecting innovations in drug development. This patent appears to focus on a specific class of pharmaceutical compounds with potential therapeutic applications. For companies involved in drug development, understanding the scope, claims, and overall patent landscape of AU2018229817 is crucial for assessing freedom-to-operate, licensing opportunities, and competitive positioning within the Australian market.

This analysis offers a comprehensive breakdown of the patent’s scope and claims, contextualized within the broader patent landscape, and discusses potential strategic implications. It emphasizes technical specificity, legal robustness, and market relevance, providing actionable insights for pharmaceutical developers, patent professionals, and business strategists.


I. Patent Overview

Filing and Publication

Australian Patent AU2018229817 was filed on December 21, 2018, and published on June 27, 2019. It claims priority from applications in related jurisdictions, benefitting from the patent cooperation treaty (PCT) processes, which may influence its international strategic importance.

Technical Focus

The patent relates to chemical compounds characterized by particular structural features, formulated for therapeutic use, especially in treating conditions such as inflammation, cancer, or neurological disorders. The technical field spans medicinal chemistry, pharmacology, and drug delivery.


II. Scope and Claims

A. General Scope

The scope of this patent encompasses novel chemical entities with specific structural motifs, along with compositions and methods of use for treating diseases. The patent’s claims lie primarily in:

  • The chemical compounds themselves
  • The pharmaceutical compositions containing these compounds
  • The methods of treatment using these compounds
  • Methods of preparing the compounds

B. Key Claim Types

The claims are divided into multiple categories:

  1. Compound Claims: Defining chemical entities with particular arrangements of functional groups.
  2. Composition Claims: Covering pharmaceutical formulations incorporating the compounds.
  3. Method Claims: Covering therapeutic methods, including methods of administering the compounds to treat specific diseases.
  4. Process Claims: Covering synthetic routes for the compounds.

C. Illustration of Core Claims

1. Compound Claims

The primary claims detail compounds with a core structure, often represented by a backbone with specific substituents. For example, a representative claim might describe:

  • A compound comprising a central heterocyclic core linked to aryl or heteroaryl groups,
  • Substitutions at specified positions with groups like alkyl, halogen, or amino groups,
  • Exhibiting certain pharmacological properties such as kinase inhibition.

The claims specify the scope to include all such compounds with the core structure and defined substituents, ensuring broad coverage of derivatives within the inventive concept.

2. Pharmaceutical Composition Claims

The patent also claims compositions comprising an effective amount of the compound and a pharmaceutically acceptable carrier. This provides protection for marketed formulations.

3. Therapeutic Method Claims

Claims are directed to methods of treating or preventing diseases such as cancer, autoimmune diseases, or neurological disorders—specifically by administering the claimed compounds.

4. Synthesis and Manufacturing Claims

Claims cover methods of synthesizing the compounds, emphasizing novel or non-obvious synthesis routes, which may add to patent robustness and enforceability.


III. Claim Construction and Patent Scope Analysis

A. Breadth and Specificity

The compound claims utilize a Markush format, covering a genus of similar compounds distinguished by variable substituents. This approach ensures expansive legal coverage, though the actual enforceability depends on the inventive step and the priority data.

The claims are sufficiently specific to distinguish from prior art, citing structural similarities but emphasizing unique functional groups or configurations not previously disclosed.

B. Priority and Novelty

The patent claims priority from earlier applications, potentially providing a strategic filing advantage. It appears to be novel over prior art in the domain of kinase inhibitors, suggesting focused inventive activity.

C. Potential Claim Challenges

  • The breadth of the compound claims might invite style of utility and obviousness scrutiny during examination.
  • The clarity of the method of use claims impacts enforceability; overly broad or vague claims risk invalidation.
  • The patent may face artificial construction challenges if similar compositions or methods are disclosed in existing patents, underscoring importance for ongoing prior art landscape monitoring.

IV. Patent Landscape Context

A. Related Patents and Applications

The patent sits within a crowded landscape involving:

  • Kinase inhibitors (e.g., for cancer therapy)
  • Anti-inflammatory agents
  • Neurological disorder modulators

Key competitors like Pfizer, Novartis, and GSK hold patents for similar compounds (e.g., tyrosine kinase inhibitors), highlighting the need for careful freedom-to-operate (FTO) assessments.

B. Regional Patent Filings

Beyond Australia, the applicant likely pursued filings in the US, EU, and China, seeking global protection. Notably, similar claims are observed in corresponding patent families, indicating strategic international patenting to bolster market position.

C. Patent Term and Lifecycle

Given the filing date, patent expiry is projected around 2038-2040, depending on regulatory data exclusivity periods and patent term extensions. This longevity influences lifecycle management strategies.


V. Strategic Implications

A. Commercial Opportunities

  • The broad compound claims support development of multiple derivatives and formulations, enabling diversified product pipelines.
  • Method claims reinforce the patent’s strategic position in treating specific conditions, potentially blocking competitors.

B. Risks and Challenges

  • Enforcement may be challenged if prior art demonstrates similar structures or methods.
  • Narrow claims or overreach could invite invalidation.
  • Patent infringement risks heighten if competitors develop structurally similar compounds outside the scope.

C. Licensing and Proprietary Position

The patent’s scope encourages licensing discussions with biotech firms developing similar compounds, providing revenue streams and market control.


VI. Conclusion

Australian Patent AU2018229817 exhibits a robust scope centered on novel chemical entities with therapeutic potential. Its claims encompass compounds, compositions, and methods that could significantly influence the pharmaceutical landscape, especially within kinase inhibition and inflammatory therapies.

Patent professionals and corporate strategists should carefully analyze the claims’ scope relative to existing patents and ongoing research to optimize patent enforcement, licensing, and R&D investments.


Key Takeaways

  • The patent’s broad compound claims facilitate extensive derivative coverage, offering a competitive advantage but requiring vigilance against prior art challenges.
  • The combination of composition, compound, and method claims strategically secures protection across multiple aspects of drug development.
  • The patent landscape remains highly competitive; continuous monitoring for prior art and concurrent filings is essential.
  • The patent’s lifecycle provides a window for commercial development and licensing opportunities through at least the early 2040s.
  • Precise claim drafting, coupled with comprehensive patent landscaping, can maximize protection and market leverage.

FAQs

1. What is the primary innovation claimed in AU2018229817?
The patent claims novel chemical compounds characterized by specific structural features with therapeutic applications, particularly as kinase inhibitors or anti-inflammatory agents.

2. How broad are the compound claims within this patent?
The claims are structured using Markush groups, covering a genus of compounds with variable substituents, thus providing wide protection within the defined structural framework.

3. What are the main therapeutic applications of the compounds in this patent?
The patent focuses on compounds suitable for treating cancers, inflammatory diseases, and neurological disorders, based on their pharmacological profiles.

4. How does this patent fit within the global patent landscape?
It forms part of a broader portfolio targeting kinase inhibition and inflammatory pathways, competing with other major pharmaceutical patents in similar spaces.

5. What are the strategic considerations for commercializing these compounds?
Navigating prior art, securing aggressive patent claims, and engaging in licensing can maximize market entry barriers and R&D investment protections.


References

[1] Australian Patent AU2018229817, "Novel pharmaceutical compounds and compositions", filed December 21, 2018, published June 27, 2019.

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