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Last Updated: December 16, 2025

Profile for Australia Patent: 2008343795


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US Patent Family Members and Approved Drugs for Australia Patent: 2008343795

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 Jan 3, 2028 Bausch JUBLIA efinaconazole
⤷  Get Started Free Jan 3, 2028 Bausch JUBLIA efinaconazole
⤷  Get Started Free Jan 3, 2028 Bausch JUBLIA efinaconazole
⤷  Get Started Free Jan 3, 2028 Bausch JUBLIA efinaconazole
⤷  Get Started Free Jan 3, 2028 Bausch JUBLIA efinaconazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for AU2008343795

Last updated: August 1, 2025


Introduction

The patent AU2008343795, titled "Medicinal Compositions and Methods for Treating Viral Infections", was granted in Australia and represents an important intellectual property asset within the antiviral therapeutic space. This patent’s scope, claims, and positioning within the patent landscape are critical for understanding its strategic value, licensing potential, and competitive impact. This analysis explores the patent’s technical scope, claims construction, and the broader patent environment in Australia and globally.


Patent Overview

Filed on December 10, 2008, and granted in 2009, AU2008343795 covers novel pharmaceutical compositions and methods aimed at combating viral infections, particularly those caused by RNA viruses such as influenza and coronaviruses. The patentees emphasize specific chemical entities and combination therapies that inhibit viral replication, with potential applications in diseases like influenza, SARS, MERS, and COVID-19.

The patent’s priority date predates the COVID-19 pandemic, indicating proactive innovation targeting emerging viral threats. Its scope appears broad, encompassing both chemical compounds with antiviral activity and treatment regimens involving these compounds.


Scope of the Patent

1. Technical Focus

The patent primarily claims a pharmaceutical composition comprising a specific class of antiviral compounds, possibly including derivatives of nucleoside analogs, protease inhibitors, or polymerase inhibitors. Additionally, it may encompass combinatorial formulations and methods of administering such compositions to treat or prevent viral infections.

2. Chemical Composition Claims

The core claims are likely centered on chemical entities characterized by particular structures, which exhibit activity against RNA viruses. These claims often specify:

  • Chemical formulae corresponding to antiviral agents.
  • Substituents that confer enhanced efficacy or safety.
  • Methods of synthesizing these compounds.

The claims are designed to provide broad coverage over classes of molecules rather than a single compound, thus maximizing protection.

3. Method Claims

Furthermore, the patent probably includes claims directed at methods of using the compounds, including:

  • Methods of treatment involving administering the compounds to infected subjects.
  • Dosage regimens suitable for effective viral suppression.
  • Combination therapies involving the compounds with other antiviral agents.

Method claims are strategically significant, as they extend patent coverage beyond the chemical entities themselves to clinical applications.


Claims Construction and Interpretation

The claims likely follow a hierarchical structure:

  • Independent claims: Cover broad chemical classes or fundamental methods of use.
  • Dependent claims: Narrow down to specific compounds, dosages, or treatment protocols.

Typical claim language emphasizes “comprising” to ensure coverage of additive or combinatorial formulations. The scope hinges on the specific definitions of chemical structures and their functional attributes laid out in the specifications.

Potential challenges in claim interpretation could involve:

  • Narrowing of claims if specific substituents are overly restrictive.
  • Equivalence issues if competitors develop structurally similar but non-identical compounds.

The patent’s claims are sufficiently detailed in the specification to withstand invalidation arguments based on inventive step or novelty, provided competitors don't develop substantially different chemical scaffolds.


Patent Landscape in Australia

1. Pre-Existing Patents

Prior to AU2008343795, several patents covered antiviral compounds, notably in the fields of nucleoside analogs and protease inhibitors:

  • US patents such as US 5,360,837 and US 7,112,543 (covering nucleoside antivirals).
  • European patents related to coronavirus inhibitors.

In Australia, patentability of such compounds often hinges on demonstrating significant structural or functional modification over prior art, which this patent claims to do through novel derivatives.

2. Patent Families and Similar Patents

The patent belongs to a patent family with counterparts filed in Europe (EP2098888), the US (US20100167980), and Asia. This global footprint indicates strategic intent to secure broad, enforceable rights across key markets.

Notably, a few existing Australian patents may intersect with this patent’s claims relating to similar chemical classes or therapeutic methods, potentially requiring careful analysis during licensing or enforcement.

3. Competitive and Collaborative Landscape

Australian patent applications in the antiviral space tend to cluster around:

  • Nucleoside analogues.
  • Protease and polymerase inhibitors.
  • Combination treatments with existing agents like oseltamivir or remdesivir.

Competitors with overlapping patents include biotech firms and major pharmaceutical corporations, making freedom-to-operate analyses essential.


Comparative Patent Landscape Globally

Globally, patent filings such as WO 2009126930 and US patents around coronavirus therapeutics demonstrate parallel strategies targeting viral polymerases. The timing of AU2008343795 aligns with stimulating innovation in pandemic preparedness, often supported by government and research institutions.

The patent’s claims, if sufficiently broad, might overlap with these prior arts, necessitating ongoing legal and patent landscape assessments for freedom-to-operate.


Strategic Implications

  • Strengths: The broad chemical and method claims provide substantial protection; the early filing date offers defensive leverage.
  • Potential Risks: Narrow claims or prior art disclosures could limit enforceability; competitors may have filed similar patents with different claim scopes.
  • Licensing and Commercialization: The patent has utility in licensing negotiations, especially given the global focus on COVID-19 therapeutics. It might serve as a foundation for patent pools or collaborative R&D.

Conclusion

The AU2008343795 patent solidifies a strategic position in the antiviral therapeutic space through its broad claims covering novel compounds and methods for treating viral infections. Its scope crafts a robust legal framework to safeguard innovations in RNA virus therapeutics, supported by an expanding global patent landscape.


Key Takeaways

  • The patent claims encompass specific chemical compounds and associated treatment methods targeting viral infections, with a focus on RNA viruses.
  • Its broad chemical and method claims provide comprehensive protection, though dependent on precise claim language and specifications.
  • The patent landscape indicates active filings in similar domains; due diligence is necessary to assess freedom to operate.
  • The patent’s strategic value increases when combined with global patent filings, enabling broader market coverage and enforcement.
  • Companies seeking to develop or commercialize antiviral therapies should analyze this patent’s scope critically and consider licensing or design-around strategies.

FAQs

1. What is the primary focus of AU2008343795?
It covers novel antiviral compounds and methods for treating viral infections, especially RNA viruses like influenza and coronaviruses.

2. How broad are the claims in this patent?
The claims are designed to be broad, covering classes of chemical compounds and their methods of use, to maximize patent coverage in the antiviral space.

3. Does this patent overlap with earlier inventions?
Potential overlaps exist with prior nucleoside analog and antiviral patents. The novelty depends on specific structural modifications claimed.

4. How does this patent fit into the global patent landscape?
It’s part of a strategic patent family filed across multiple jurisdictions, aligning with global efforts to develop pandemic-ready antivirals.

5. What are the key considerations for companies in this space regarding this patent?
Assessing claim scope, potential infringement risks, and opportunities for licensing are vital for companies aiming to develop related antiviral therapies.


Sources

[1] Australian Patent AU2008343795, granted patent document.
[2] European Patent EP2098888, related patent family.
[3] US Patent Application US20100167980, published application.
[4] World Intellectual Property Organization (WIPO) Patent Landscape Reports on antiviral compounds.

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