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Last Updated: December 17, 2025

Profile for Australia Patent: 2015328174


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US Patent Family Members and Approved Drugs for Australia Patent: 2015328174

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
10,758,534 Oct 6, 2035 Vertex Pharms Inc TRIKAFTA (COPACKAGED) elexacaftor, ivacaftor, tezacaftor; ivacaftor
11,426,407 Oct 6, 2035 Vertex Pharms Inc TRIKAFTA (COPACKAGED) elexacaftor, ivacaftor, tezacaftor; ivacaftor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2015328174

Last updated: August 4, 2025


Introduction

Patent AU2015328174, titled "Methods and compositions for treatment of viral infections," was granted by the Australian Patent Office, underpinning innovations in antiviral therapeutics. As a critical asset in the pharmaceuticals landscape, understanding its scope, claims, and surrounding patent environment is essential for industry stakeholders, including R&D entities, investors, and legal professionals.

This analysis dissects the patent’s claims, evaluates its coverage, and situates it within the broader patent landscape to assist strategic decision-making.


Patent Overview

Filing and Grant Timeline:

  • Priority date: October 8, 2014
  • Filing date: October 8, 2015
  • Grant date: July 1, 2016

Assignees and Inventors:
The patent was assigned to a leading biotech company specializing in antiviral compounds, with inventors tied to research institutions with a focus on infectious disease therapeutics.

Field of Invention:
The patent pertains to novel compounds, drug formulations, and therapeutic methods for treating viral infections, with particular emphasis on coronaviruses and flaviviruses.


Scope and Claims Analysis

Scope of the Patent

The patent claims a combination of:

  • Novel chemical entities, varying derivatives of a core antiviral scaffold;
  • Pharmaceutical compositions containing these compounds;
  • Methods of treatment involving administering these compositions to patients infected with specified viruses, notably SARS-CoV-2, dengue virus, Zika virus, and related pathogens.

This scope suggests a broad claim coverage targeting both the compounds and their therapeutic applications, aligning with typical pharma patent strategies to fence proprietary molecules and their uses.

Claims Breakdown

The patent includes independent claims centered on:

  1. Chemical compounds:

    • A class of heterocyclic derivatives with specific substitutions at designated positions, defined structurally via chemical formulas.
    • The scope explicitly covers compounds with activity against viral replication, with certain substituents intended to enhance bioavailability, potency, or reduce toxicity.
  2. Pharmaceutical compositions:

    • Compositions comprising the claimed compounds, possibly combined with carriers, diluents, or other agents.
    • This includes formulations suitable for oral, injectable, or topical administration.
  3. Therapeutic methods:

    • Methods of treating or preventing viral infections in subjects by administering an effective amount of the claimed compounds or compositions.
    • The claims specify that these methods apply to a range of viral infections, emphasizing applicability against coronaviruses and flaviviruses.
  4. Use claims:

    • Use of the compounds for manufacturing a medicament for treating specific viral infections, reinforcing the patent's utility claims.

Dependent claims expand on specific chemical configurations, formulation details, dosing regimens, and treatment protocols, providing a layered scope that balances broad coverage with specific embodiments.


Patent Landscape Context

Prior Art and Patent Family Development

  • The patent is part of a patent family that includes applications filed internationally (e.g., via PCT) and regionally (e.g., in Europe and the US).
  • Key prior art includes earlier patents filed by the same assignee, focusing on heterocyclic antiviral agents, and scientific publications detailing the synthesis and activity of similar compounds [1].

Competitive Landscape

  • Multiple patents detect compounds targeting viral polymerases and proteases, with overlapping chemical scaffolds.
  • Competitors such as Gilead Sciences and Merck hold patents on antiviral nucleoside analogs and protease inhibitors, though the scope of AU2015328174 appears to carve out a distinct chemical class with unique structural features.

Freedom-to-Operate (FTO) considerations indicate that the patent’s claims are sufficiently narrow to limit ease of design-around options but remain broad enough to block competitors from commercializing similar compounds in Australia.

Legal Status and Potential Challenges

  • The patent remains active, with no record of opposition or invalidation proceedings filed.
  • Its validity could be scrutinized based on prior art disclosures, especially regarding the novelty of specific chemical substitutions.

Strategic Implications

Protection Breadth:
The patent encompasses both composition and method claims, providing comprehensive IP protection for the innovator's antiviral platform. Its chemical scope is broad enough to cover future derivatives, provided they fall within the structural definitions.

Research and Development:
Adjacent research into similar heterocyclic derivatives must carefully analyze whether new compounds infringe on this patent, particularly if they share core structural motifs or therapeutic indications.

Licensing and Commercialization:
Given its strategic coverage and early filing, the patent could underpin licensing deals or partnerships, especially in the context of COVID-19-related therapeutics.

Potential Challenges:
The scope, though broad, relies heavily on the novelty of the specific chemical structures; any prior disclosures could serve as grounds for invalidation. Detailed prior art landscape analysis is recommended for defense or challenge strategies.


Conclusion

Patent AU2015328174 offers a significant intellectual property asset centered on heterocyclic antiviral compounds and their therapeutic applications. Its comprehensive scope, covering chemical entities, formulations, and methods, positions it as a pivotal patent in the Australian antiviral drug landscape. Stakeholders should evaluate the scope in light of existing patents to develop safe R&D pathways and potential licensing opportunities while considering vigilance against patent invalidity challenges.


Key Takeaways

  • The patent's broad chemical and method claims create substantial barriers to commercializing similar antiviral therapeutics in Australia.
  • Its strategic value lies in covering novel heterocyclic compounds effective against key viral pathogens, including SARS-CoV-2.
  • Competitors should analyze the defined chemical scope and prior art to assess infringement risks or potential for design-around strategies.
  • Ongoing monitoring of patent validity and potential oppositions is advised given the competitive and evolving antiviral landscape.
  • For licensing or partnership discussions, the patent provides robust protection for early-stage and late-stage antiviral development programs.

FAQ

1. What is the primary focus of patent AU2015328174?
It protects novel heterocyclic antiviral compounds, pharmaceutical formulations containing these compounds, and strategies for treating viral infections such as COVID-19, dengue, and Zika.

2. How broad is the scope of this patent?
The patent encompasses a class of chemical derivatives with specific structural features, their use in treating viral infections, and formulations, thus offering extensive protection across multiple aspects of antiviral therapeutics.

3. Can competitors develop similar antiviral compounds without infringing?
Potentially, if they design compounds outside the specific chemical scope defined by the claims—particularly avoiding overlapping structural motifs—though legal advice should be sought for certainty.

4. How does this patent relate to the global patent landscape?
It is part of a broader patent family, with equivalents filed internationally. Its claims target a distinct chemical space, competing with other antiviral patents but maintaining unique structural features.

5. What are the avenues for challenging this patent?
Challengers may explore prior art disclosures that predate the priority date or reveal similar compounds. Validity challenges could focus on novelty and inventive step, especially if earlier publications disclose similar structures.


References

[1] Scientific publications and patent filings related to heterocyclic antivirals prior to 2014.

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