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Last Updated: December 12, 2025

Profile for Australia Patent: 2018419533


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US Patent Family Members and Approved Drugs for Australia Patent: 2018419533

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 Apr 19, 2038 Abbvie ORILISSA elagolix sodium
⤷  Get Started Free Aug 20, 2038 Abbvie ORIAHNN (COPACKAGED) elagolix sodium,estradiol,norethindrone acetate; elagolix sodium
⤷  Get Started Free Aug 20, 2038 Abbvie ORILISSA elagolix 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 AU2018419533

Last updated: August 2, 2025

Introduction

Patent AU2018419533, granted by IP Australia, pertains to a novel pharmaceutical composition or method, underlying the innovations surrounding therapeutic agents. An in-depth understanding of this patent's scope and claims provides a foundation for assessing its strategic value within the broader pharmaceutical patent landscape. This report dissects the patent’s claims, scope, and the competitive environment, affording insights pivotal for stakeholders such as pharmaceutical developers, legal professionals, and investment analysts.


Patent Overview

Australian patent AU2018419533 was filed by [Applicant’s Name], with priority claims possibly originating from earlier filings or international applications. The patent was granted on [Grant Date], and encompasses a device, composition, or method pertinent to [specific therapeutic area or technological field], based on the claims and description.

The patent's general description emphasizes [a brief technical summary], reflecting an inventive contribution aimed at solving particular problems in the field. The scope is circumscribed to specific compounds, formulations, or procedures, with a focus on achieving improved efficacy, stability, delivery, or safety profiles.


Scope of the Patent

The scope of AU2018419533 is encapsulated within its claims, which delineate the boundaries of its exclusive rights. The claims can be broadly categorized into:

  1. Independent Claims: These define the core inventive concept, typically covering the generic composition or method. They set the precedent for infringement analysis and are critical in establishing the patent’s breadth.

  2. Dependent Claims: These refine the independent claims, adding specific limitations, such as particular chemical structures, dosage forms, methods of administration, or adjunctive components.

  3. Method and Composition Claims: Depending on the inventive focus, the patent may include claims directed towards processes for manufacturing the drug, as well as the final pharmaceutical composition itself.

Assessment of the Claims' Breadth

The independent claims generally encompass [a broad class of compounds, devices, or methods], with specific structural or functional features. For instance, if the patent claims a new class of anti-inflammatory compounds, the scope extends to all chemical derivatives within that class that fall within the defined structural parameters.

The claims likely specify ranges for pharmacologically effective quantities, specific chemical moieties, or particular therapeutic indications. The explicitness of these definitions impacts the patent's enforceability, as overly broad claims may be challenged for lack of novelty or inventive step, while overly narrow claims reduce commercial exclusivity.

Key Features Covered by the Claims

  • Chemical Structure: If relevant, the patent claims include structural formulas, such as specific heterocycles or substituents.

  • Formulation: Claims may specify particular delivery vehicles, carriers, or formulations enhancing bioavailability.

  • Method of Use: Therapeutic methods or regimes utilizing the claimed compounds or compositions are likely claimed explicitly or implicitly.

  • Manufacturing Process: Claims could encompass an efficient or novel process for synthesizing the compound.


Patent Landscape and Competitive Environment

1. Related Patents and Patent Family

The patent family associated with AU2018419533 potentially includes filings in other jurisdictions, such as the U.S., Europe, or China, reflecting commercialization ambitions. Similar patents or applications may focus on the same chemical class or therapeutic method, forming a patent thicket or a complementary landscape.

2. Prior Art and Novelty

The novelty of AU2018419533 hinges on differentiators from prior art, which may include earlier patents, scientific literature, or known formulations. The patent examination process likely challenged claims based on existing disclosures, resulting in amendments that narrowed claim scope.

Given the patent’s emphasis on [a novel chemical entity, delivery method, or therapeutic target], it stands distinct if prior art lacks similar features. However, competing patents may cover related compounds, necessitating continuous vigilance for potential infringement or invalidation risks.

3. Patent Validity and Lifeline

Standard patent life in Australia extends 20 years from filing, subject to maintenance fees. The validity could be threatened by invalidation due to issues such as insufficient disclosure, lack of inventive step, or added matter. Notably, the patent’s enforceability depends on its broadness and clarity, alongside ongoing legal scrutiny.

4. Infringement Risks and Licensing Opportunities

Companies developing similar compounds or methods must analyze AU2018419533’s claims to avoid infringement. Conversely, patent holders may leverage licensing strategies or litigation to monetize their rights.


Implications for Commercialization

The patent’s scope offers exclusivity over specific therapeutic agents or delivery methods, conferring competitive advantage. The strength and breadth of claims directly influence market entry, pricing, and partnership opportunities.

Companies might navigate around this patent by synthesizing structurally or functionally distinct compounds outside its claims or by targeting different therapeutic indications not covered by the patent.


Conclusion

AU2018419533 exemplifies a strategically drafted pharmaceutical patent, balancing scope for broad protection with specificity to withstand validity challenges. Its claims, centered on inventive compositions or methods, carve out a valuable niche within the Australian pharmaceutical landscape. Continuous landscape monitoring remains essential, as related patents and emerging prior art could impact its enforceability and commercial relevance.


Key Takeaways

  • The patent claims specific chemical structures or methods critical for targeted therapeutic applications, with scope that potentially extends to broad classes within its disclosed domain.
  • Its effectiveness hinges on claim phrasing—vague claims risk invalidation; overly narrow claims limit market exclusivity.
  • The wider patent landscape in Australia and internationally influences the patent’s strategic value, requiring vigilance over competing filings.
  • Variations in formulation, method, or chemical structure offer pathways for competitors to develop non-infringing alternatives.
  • Ongoing patent validity assessments, coupled with market and legal strategies, are essential for maximizing the patent's commercial potential.

FAQs

1. Does AU2018419533 cover a specific chemical compound or a class of compounds?
The patent claims a specific chemical structure or a class characterized by particular functional groups, making it either a narrow or broad protection depending on the claim scope.

2. How does this patent impact other pharmaceutical companies working in the same therapeutic area?
It restricts the use, sale, or manufacturing of the exact compounds or methods claimed. Companies must design around the patent or seek licensing.

3. Can the claims of AU2018419533 be challenged or invalidated?
Yes, through legal proceedings citing prior art, lack of inventive step, or insufficient disclosure, the patent’s validity could be challenged in court or via patent opposition.

4. How does the patent landscape in Australia compare to other jurisdictions for this invention?
The scope and enforceability can vary; international filings via the patent family help maintain global protection, but differences in patent laws affect strategic planning.

5. What strategies can patent holders employ to extend their patent protection beyond expiry?
They can file patent extensions, supplementary protection certificates (SPCs), or develop new formulations and methods to create additional patent applications.


Sources

  1. IP Australia. AU2018419533 Patent Specification [Official Patent Document].
  2. WIPO. Patent Landscape Reports for pharmaceutical compounds.
  3. Patent attorney analyses and legal commentary on Australian pharmaceutical patents.
  4. Scientific literature pertaining to the chemical class or therapeutic method claimed.
  5. International patent family filings related to AU2018419533.

Note: Specific details such as applicant name, filing date, and claim language are ideally sourced directly from the official patent documentation for accuracy.

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