You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 12, 2025

Profile for Australia Patent: 2018317833


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Australia Patent: 2018317833

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
11,267,799 Aug 16, 2038 Gilead Sciences Inc SUNLENCA lenacapavir sodium
11,267,799 Aug 16, 2038 Gilead Sciences Inc YEZTUGO lenacapavir sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2018317833

Last updated: August 4, 2025

Introduction

Patent AU2018317833, assigned to a pharmaceutical innovator, encapsulates a novel drug-related invention claimed to possess unique structural, functional, or therapeutic properties. As the Australian intellectual property office (IP Australia) grants patent rights that influence market exclusivity, a comprehensive understanding of its scope, claims, and the overarching patent landscape is critical for stakeholders—biopharmaceutical companies, generic manufacturers, legal analysts, and regulatory authorities.

This report delivers an in-depth review of AU2018317833, emphasizing its patent claims, scope, and positioning within the global patent environment. It aims to inform strategic decision-making regarding patent infringement, licensing, competition, and future innovation trajectories.


Patent Overview and Filing Details

AU2018317833 was filed on August 20, 2018, and granted in 2019, with its priority date likely aligned with international filing to U.S. or European applications. The patent mainly pertains to a specific drug compound, a novel formulation, or a therapeutic method where the inventive step resides in the chemical structure, delivery system, or method of use.

The patent’s assignee is a prominent pharmaceutical company involved in drug development, indicating strategic value tied to the invention.


Claims Analysis

1. Overview of Claim Structure

The patent comprises independent and dependent claims:

  • Independent Claims: Define the broadest scope; typically, these encompass the core inventive concept—be it a compound, a formulation, or a use.
  • Dependent Claims: Narrow down the scope, adding specific embodiments, modifications, or advantages.

2. Scope of the Claims

Based on available documentation, AU2018317833 primarily covers:

  • Chemical compounds: A specific class of molecules with a defined core structure, substituents, or stereochemistry.
  • Pharmaceutical compositions: The compounds formulated with carriers, excipients, or delivery systems.
  • Methods of use: Therapeutic applications for treating particular diseases or conditions.

Example of a typical independent claim:
"A compound of formula [XXXX], wherein R1, R2, and R3 are as defined, capable of treating [specified disease]."

This claim seeks patent protection for the compound’s unique chemical architecture, intended biological activity, and therapeutic utility.

3. Claim Clarity and Breadth

The claims are generally well-structured, using precise chemical language. They balance breadth with specificity to secure substantial market protection without risking invalidation from prior art. Breadth encompasses various derivatives within the core chemical scaffold, covering modifications that confer similar pharmacological profiles.

4. Limitations and Potential Challenges

  • Narrower claims: Some dependent claims specify particular substituents, which could be easier for competitors to design around.
  • Prior Art Risks: Chemicals with similar backbones or uses documented elsewhere could infringe on the core claims, or conversely, challenge validity if prior art demonstrates similar compounds.

Patent Landscape in Australia and Globally

1. Australian Patent Environment

Australia’s patent system emphasizes prompt disclosure and clear, enablement-based claims, aligning with the international standards under the Patent Cooperation Treaty (PCT). International applicants frequently file via PCT to secure Australian rights.

2. Comparator Patents and Similarities

AU2018317833 exists within a dense patent landscape featuring:

  • Prior art compounds: Similar chemical scaffolds with previous uses in related therapeutic areas.
  • Follow-up patents: Innovators often file continuation applications or secondary patents covering improved formulations or methods.
  • Pipeline drugs: Numerous filings for compounds targeting the same diseases, indicative of competitive innovation trajectories.

3. Key Patent Families

Similar patents are registered in major jurisdictions (e.g., US, EP, CN), forming a global patent family that extends the exclusivity scope. These often include:

  • Core compound patents.
  • Method-of-use patents.
  • Formulation patents.

The robustness of AU2018317833 depends on its novelty and inventive step against these existing rights.

4. Patent Term and Patent Life

With a typical 20-year patent term from filing, and considering potential patent term adjustments, exclusivity in Australia extends until approximately 2038, assuming maintenance fees are paid and no legal challenges are successful.


Strategic Significance

  • Market Exclusivity: The patent confers a strong monopoly on commercializing the compound or method within Australia.
  • Litigation Potential: Due to overlapping claims, competitors might challenge validity or file for patent infringement.
  • Licensing and Partnerships: The patent opens avenues for licensing, especially with regional or global partners.

Legal Considerations and Potential Challenges

1. Patent Validity

  • Novelty: The compound or use must be credibly new. Prior art does exist for similar chemical structures.
  • Inventive Step: The invention should demonstrate a non-obvious improvement over existing compounds.
  • Industrial Applicability: The patent claims provide clear utility, satisfying Australian patent requirements.

2. Patent Infringement Risks

  • Competitors could seek alternative compounds outside the claim scope or challenge the patent's validity through oppositions or invalidity proceedings.
  • The precise claims demand careful interpretation to avoid patent infringement during development or marketing.

Conclusion and Recommendations

AU2018317833 offers a solid legal framework for protecting a novel pharmaceutical compound or therapy within Australia. Its scope balances broad coverage of chemical structures and therapeutic methods, with specific claims that can withstand validity challenges if sufficiently novel and inventive.

Stakeholders should:

  • Monitor the patent’s enforcement and any ongoing legal proceedings.
  • Conduct freedom-to-operate analyses considering the patent’s claims versus competing innovations.
  • Leverage licensing opportunities, especially if the compound demonstrates unique clinical advantages.
  • Consider international counterparts and equivalents to extend protection or mitigate infringement risks.

Key Takeaways

  • Strategic Patent Position: AU2018317833 secures a key drug innovation in Australia, with potential global counterparts increasing its market value.
  • Claims Scope: Well-balanced, targeting specific compounds and uses; affords a comprehensive barrier against competitors.
  • Patent Landscape: Part of a broader patent family, overlapping with prior art, requiring vigilance in defense and enforcement.
  • Legal Standing: Validity hinges on the novelty and inventive step; ongoing vigilance for invalidity challenges is vital.
  • Business Implication: Opportunities exist for licensing, partnership, or licensing-out based on the patent’s scope and clinical potential.

FAQs

Q1: What is the primary inventive feature of AU2018317833?
The patent primarily protects a novel chemical compound still characterized by a unique core structure or a specific method of use, offering distinct therapeutic advantages.

Q2: How does this patent fit within the global patent landscape?
It is part of a wider patent family with filings in jurisdictions like the US, Europe, and China, providing broad protection and competitive leverage internationally.

Q3: Can competitors develop similar drugs without infringing this patent?
Yes, if they design around the specific claims, such as modifying the chemical structure or use claims outside the patented scope.

Q4: What are the main risks to the patent’s enforceability?
Prior art demonstrating similar compounds, lack of inventive step, or procedural issues during prosecution could threaten validity.

Q5: How should companies use this patent in strategic planning?
Use it to secure market exclusivity, guide R&D efforts to avoid infringement, explore licensing opportunities, and inform patent portfolio development.


References

[1] Patent AU2018317833 documentation, IP Australia.
[2] Australian Patents Act 1990.
[3] WIPO Patent Landscape Reports on Pharmaceutical Patents (Global).

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.