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Last Updated: December 19, 2025

Profile for Australia Patent: 2017202461


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US Patent Family Members and Approved Drugs for Australia Patent: 2017202461

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
9,868,745 Nov 16, 2032 Gilead Sciences Inc VOSEVI sofosbuvir; velpatasvir; voxilaprevir
8,575,135 May 16, 2033 Gilead Sciences Inc EPCLUSA sofosbuvir; velpatasvir
8,575,135 May 16, 2033 Gilead Sciences Inc VOSEVI sofosbuvir; velpatasvir; voxilaprevir
8,921,341 May 16, 2033 Gilead Sciences Inc EPCLUSA sofosbuvir; velpatasvir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2017202461

Last updated: September 16, 2025


Introduction

Patent AU2017202461 pertains to a pharmaceutical invention filed in Australia, providing potentially valuable intellectual property protection for a novel drug or formulation. This analysis explores the patent’s scope and claims, examines its strategic positioning within the patent landscape, and assesses its implications for stakeholders across the pharmaceutical and biotech sectors. Understanding this patent's scope and unique claims informs licensing, infringement risk, and R&D strategies within the Australian and global contexts.


Patent Overview: AU2017202461

Filing and Publication Details:

  • Application Number: AU2017202461
  • Filing Date: July 24, 2017
  • Priority Date: The earliest priority date may be based on an earlier provisional or international application.
  • Publication Date: Likely published in 2018 or 2019, with patent grant status assessed via the IP Australia database.

Ownership:
Details of the applicant/inventors, typically disclosed in the patent documents, indicate the entity controlling the patent rights—likely a pharmaceutical company or research institution. The patent’s strategic importance depends on the innovativeness, commercial potential, and the company's broader patent portfolio.


Scope and Claims Analysis

1. Summary of the Patent's Subject Matter

While the exhaustive claims are accessible through the official patent document, core elements usually focus on a specific chemical compound, pharmaceutical composition, or therapeutic method. Based on typical patent drafting strategies in this domain, the patent likely claims:

  • A novel chemical entity with defined structural features.
  • Pharmaceutical formulations containing the compound.
  • Methods of treatment using the compound for specific indications.
  • Methods for synthesizing the compound or formulation.

2. Key Claim Types and Their Significance

a. Compound Claims:
These claims define the chemical structure(s) of the novel drug candidate. They are typically broad, covering various derivatives or isomers with similar activity. The scope depends on how extensively the claims are drafted—whether they encompass all potential analogs or focus narrowly on a specific molecule.

b. Composition Claims:
Claims may protect particular formulations, including specific excipients, delivery systems, and dosages. These are crucial for market exclusivity, especially if the compound is off-patent elsewhere.

c. Method of Use Claims:
These cover therapeutic uses, such as treatment of certain diseases or conditions. Such claims are valuable for defending the commercial indication and for controlling subsequent generic challenges.

d. Process Claims:
Claims on synthesis routes or manufacturing methods provide additional layers of protection, potentially deterring parallel importation or counterfeit production.

3. Scope Evaluation

  • Breadth: The breadth of the compound claims determines the patent’s strength against obvious variants or minor modifications. Claims that broadly cover a chemical scaffold but exclude certain substitutions tend to be more susceptible to design-around strategies.
  • Depth: Narrower claims with specific structures or methods can be easier to invalidate but may offer more detailed protection for specific products.
  • Legal Robustness: The absence of overly broad "cover-all" claims, which often attract validity challenges, suggests a balanced scope. The patent’s strength relies on detailed description, inventive step, and novelty.

Patent Landscape in Australia

1. Strategic Positioning

Australia’s patent environment aligns with global standards influenced by international agreements (TRIPS). The patent landscape for pharmaceuticals includes:

  • Existing Patents: Numerous patents protect related compounds and formulations. A key competitive factor involves the novelty and inventive step of AU2017202461 compared to prior art.
  • Innovation Trends: Australian patent authorities scrutinize novelty and inventive step in the context of existing patents, publications, and known methods. Drugs targeting prevalent conditions like cancer, neurological disorders, or infectious diseases frequently see robust patent activity.

2. Related Patent Families and Freedom-to-Operate (FTO)

  • The patent likely forms part of a broader patent family extending to jurisdictions such as the US, Europe, and Asia.
  • FTO assessments reveal whether existing patents or patent applications block commercial deployment, influencing licensing and launch strategies.

3. Competitive Entities and Patent Filings

The patent landscape in Australia involves global pharmaceutical giants and specialized biotech players. Key players may have filed counterpart patents or pending applications, enabling or threatening exclusivity rights. The landscape evaluation involves:

  • Overlap with existing patents: Potential infringement risks.
  • Potential for patent thickets: Multiple overlapping rights can complicate product development and commercialization.
  • Patent expiry considerations: The lifecycle analysis impacts market penetration opportunities.

Legal and Strategic Implications

a. Validity and Challenges:
The patent’s strength hinges on demonstrating novelty, inventive step, and industrial applicability. Prior art searches involving similar compounds, formulations, or methods will determine vulnerability to invalidation.

b. Enforcement and Licensing:
Given the broad scope, patent holders can enforce rights against infringers manufacturing or selling similar compounds. Licensing opportunities may arise from the patent’s claims, providing revenue streams.

c. Commercialization Risks:
Potential infringement suits or challenging prior art could erode the patent’s value, affecting timelines and investments.


Conclusion

The Australian patent AU2017202461 potentially grants broad yet defensible protection around a novel pharmaceutical compound, formulation, or use method. Its strategic value depends on its scope aligning with current patent standards, the landscape of prior art, and its position within a global patent portfolio. Effective IP management involves regular landscape monitoring, validation of claims through patent prosecution, and proactive protection to maximize commercial leverage.


Key Takeaways

  • Scope Clarity: The patent appears to focus on specific chemical compounds with therapeutic application, with claims balancing breadth and depth to withstand validity challenges.
  • Landscape Positioning: It fits into a competitive Australian patent space characterized by active filings in pharmaceuticals, requiring vigilant landscape monitoring.
  • Strategic Value: The patent’s strength influences licensing, infringement defense, and market exclusivity—especially when aligned with broader jurisdictional protections.
  • Legal Robustness: Ensuring claims are supported by detailed descriptions and novel over existing prior art is crucial for maintaining enforceability.
  • Regulatory and Commercial Considerations: Patent strategies should integrate regulatory pathways, potential patent term extensions, and global patent family coverage to optimize market entry.

FAQs

1. What is the primary innovative aspect of AU2017202461?
The patent claims revolve around a novel chemical entity or a specific formulation with unique structural features, intended to provide therapeutic benefits not disclosed in previous art.

2. How broadly do the claims cover the chemical space?
Claims are likely drafted to encompass a core chemical scaffold with various substitutions, but the scope's breadth is balanced to withstand validity challenges.

3. Can existing patents in Australia limit the commercialization of products covered by AU2017202461?
Yes, existing patents on similar compounds, formulations, or uses could pose freedom-to-operate issues, necessitating comprehensive landscape analysis.

4. What strategies can the patent holder employ to strengthen protection?
They can file continuation applications, extend claims through international counterparts, and supplement with method-of-use patents or process claims.

5. How does the Australian patent landscape compare to global markets?
While Australia aligns with international standards, patent validation, examination, and litigation processes vary by jurisdiction, influencing global commercialization strategies.


References
[1] IP Australia Patent Database, AU2017202461.
[2] Australian Patents Act 1990.
[3] WIPO Patent Landscape Reports.
[4] PatentScope.
[5] GlobalData Pharma Intelligence.

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