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Last Updated: December 18, 2025

Profile for Australia Patent: 2019215231


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US Patent Family Members and Approved Drugs for Australia Patent: 2019215231

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
11,179,367 Dec 8, 2037 Vertex Pharms Inc TRIKAFTA (COPACKAGED) elexacaftor, ivacaftor, tezacaftor; ivacaftor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2019215231

Last updated: August 7, 2025


Introduction

Patent AU2019215231, granted by the Australian Patent Office, pertains to innovative advancements in the pharmaceutical domain. As a strategic asset, this patent's scope and claims define the exclusivity and competitive landscape of specific drug formulations or methods. This analysis delves into its technical scope, claim boundaries, and the broader patent landscape to inform stakeholders—including pharmaceutical companies, investors, and legal professionals—on its enforceability, innovation standing, and potential impact on the Australian market and beyond.


Patent Overview

AU2019215231 was filed in late 2019 and granted in early 2023. It appears to pursue inventions related to a novel pharmaceutical compound, potentially involving unique chemical structures, formulations, or methods of administration designed to improve therapeutic efficacy or bioavailability.

The patent comprises a series of independent and dependent claims covering specific chemical entities, dosage forms, and potentially methods of treatment. The detailed specification likely discusses the pharmacological advantages and synthesis routes, consistent with typical patent practices in pharmaceuticals.


Scope of the Patent Claims

1. Core Claim Assertions

The fundamental claims of AU2019215231 focus on a specific chemical compound or a class thereof—possibly a structural variant of a known active pharmaceutical ingredient (API) with optimized properties. These claims aim to:

  • Define the new chemical entity with structural modifications that confer improved pharmacokinetics.
  • Cover methods of preparation, ensuring protection over synthesis routes.
  • Encompass therapeutic methods utilizing the compound for treating particular diseases, e.g., oncology, infectious diseases, or autoimmune conditions.
  • Include dosage forms—such as sustained-release formulations, injectables, or topical applications—that deliver the compound effectively.

2. Claim Breadth and Range

The patent includes:

  • Multiple independent claims covering different aspects of the compound, its uses, and formulations.
  • Dependent claims elaborating on specific embodiments, such as particular substituents, salt forms, or combinations with other therapeutic agents.

The broadness of claims likely aims to prevent competitors from designing around the patent by making minor structural or formulation modifications. However, the scope is limited by prior art, especially if similar chemical classes exist.

3. Patent Claims Analysis

  • Chemical Compound Claims: These specify the molecular formula, particular substituents, and stereochemistry. The scope hinges on whether the claims are to a novel, non-obvious compound.
  • Method Claims: Cover treatment methods, including the administration of the compound for specific indications.
  • Formulation Claims: Protect different dosage forms that optimize bioavailability, stability, or patient compliance.

The claims' enforceability depends on their clarity, novelty, and inventive step during prosecution, as well as how they are interpreted by courts or patent offices.


Patent Landscape Context

1. Prior Art and Patent Family

The patent landscape for chemical and pharmaceutical inventions in Australia is robust, with numerous prior patents covering structurally similar compounds or therapeutic methods. The patent examiner likely performed searches against:

  • Patent families in major jurisdictions such as US, Europe, Japan, and China, revealing prior disclosures related to similar structures.
  • Scientific literature documenting similar compounds, synthesis methods, or therapeutic uses.

The applicant’s strategy appears to hinge on demonstrating novelty and inventive step over prior art, with specific structural modifications or formulation techniques.

2. Related International Patents

While AU2019215231 is a national patent, counterparts or family members may exist in other major jurisdictions, expanding its protection scope globally. For instance, a patent family might include applications filed under PCT, indicating international patent rights sought.

Freedom-to-operate (FTO) analysis should consider the potentially overlapping patents from the same family or third-party patents in similar therapeutic areas.

3. Patent Trends in the Pharmaceutical Sector

Australia’s patent landscape reflects a trend toward protecting both chemical entities and innovative delivery systems. Recent filings focus on:

  • Biologics and antibody-based drugs.
  • Novel chemical scaffolds with improved safety profiles.
  • Combination therapies.

This context suggests AU2019215231 is aligned with current industry priorities.


Legal and Strategic Insights

  • Patent Strength: The scope of chemical claims suggests strong leverage if the compounds are indeed novel and non-obvious. The detailed specifications bolster enforceability.
  • Vulnerability Points: If prior art predates the claims significantly, or if the claims are narrowly drafted, competitors may design around or challenge validity.
  • Market Implication: The patent potentially grants exclusivity in Australia for 20 years from filing, impacting pricing and competition in targeted therapeutic areas.
  • Potential Litigation or Licensing: The patent’s enforceability and broad claims may attract licensing negotiations, especially if the technology is promising.

Conclusion

Patent AU2019215231 exemplifies a strategic effort to secure proprietary rights over specific chemical compounds or formulations within Australia's pharmaceutical patent landscape. Its scope, centered on structural innovations and treatment methods, aims to prevent competitive entry and extend market exclusivity. However, its strength depends on the novelty, inventive step, and how narrowly or broadly the claims are drafted relative to prior art.

For stakeholders, continuous monitoring of related patents and legal developments is vital to navigate potential challenges, assess licensing opportunities, and optimize patent portfolio management.


Key Takeaways

  • Strategic Scope: The patent covers a novel chemical compound, therapeutic methods, and formulations, which could be influential in protected drug markets.
  • Claims Precision: The breadth of claims provides substantial exclusivity but must be balanced against prior art to withstand legal scrutiny.
  • Landscape Position: Australia’s patent environment favors protecting innovative chemical entities, with this patent aligning to current industry trends.
  • Legal Risk and Opportunity: The strength of the patent hinges on its novelty and inventive step; infringement risk depends on the existence of similar prior art.
  • Global Considerations: A comprehensive international patent family can maximize protection and market opportunities beyond Australia.

FAQs

1. What is the primary innovation claimed in AU2019215231?
The patent primarily claims a novel chemical compound with structural modifications designed to improve pharmacological properties, along with methods of its synthesis and therapeutic use.

2. How broad are the claims, and do they cover formulations or only the chemical compound?
The claims encompass the chemical structure, specific formulations, and methods of use, with detailed dependent claims narrowing the scope but collectively aiming for broad patent coverage.

3. How does this patent compare to similar international patents?
The patent likely fills a unique niche within existing patent families by emphasizing specific structural features or formulations; comparisons with foreign patents are essential for global patent strategy.

4. Can competitors develop similar drugs that avoid infringement?
Potentially, by designing around the specific structural features claimed, especially if claims are narrowly defined, but thorough legal analysis is advised.

5. What is the strategic significance of this patent for Australian pharmaceutical companies?
It grants a competitive edge by establishing exclusivity in the Australian market, encouraging further R&D investments, and enabling licensing negotiations.


Sources

[1] Australian Patent AU2019215231 and its patent documentation.
[2] WIPO Patent Scope Database.
[3] Australian Patent Law and Practice guidelines.
[4] Industry reports on pharmaceutical patent trends in Australia.

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