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Last Updated: December 15, 2025

Profile for Australia Patent: 2023251492


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US Patent Family Members and Approved Drugs for Australia Patent: 2023251492

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 Oct 17, 2036 Abbvie RINVOQ upadacitinib
⤷  Get Started Free Oct 17, 2036 Abbvie RINVOQ upadacitinib
⤷  Get Started Free Oct 17, 2036 Abbvie RINVOQ upadacitinib
⤷  Get Started Free Oct 17, 2036 Abbvie RINVOQ upadacitinib
⤷  Get Started Free Oct 17, 2036 Abbvie RINVOQ upadacitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2023251492

Last updated: July 28, 2025


Introduction

Patent AU2023251492 pertains to a novel pharmaceutical invention registered within Australia's patent system. As with any patent, its scope, claims, and surrounding patent landscape fundamentally influence its enforceability, commercial viability, and competitiveness. This analysis delves into the patent’s scope and claims to decipher its innovative perimeter and evaluates its position within the broader patent landscape for pharmaceuticals in Australia.


Patent Overview and Technical Domain

AU2023251492 is classified within the pharmacological domain, specifically targeting a new chemical entity, formulation, or application relevant to medicinal chemistry. Based on the application data (filing date, priority, and description), it appears to focus on a novel compound or a specific therapeutic use, potentially involving a specific method of synthesis, delivery system, or a pharmaceutical composition.

The patent's explicit claims define the scope of protection, encompassing the invention's core technical features, while the description offers detailed backing and possible embodiments.


Scope of the Patent

Legal Scope and Nature of Protection

The scope hinges on the claims, which articulate the essential features that delineate the inventor’s rights. The patent likely includes multiple claims, ranging from independent claims that cover broad inventive concepts to dependent claims providing specific embodiments.

In pharmaceutical patents, scope can encompass:

  • Compound Claims: Covering the chemical entities themselves, often with defined structural formulas.
  • Method Claims: Covering processes such as synthesis, formulation, or administration.
  • Use Claims: Covering therapeutic methods or indications.
  • Formulation Claims: Covering specific drug delivery systems or excipient combinations.

The patent’s independent claims probably focus on:

  • A chemical compound or class thereof (e.g., a new molecule or derivative).
  • Novel synthesis or manufacturing methods.
  • Therapeutic use of the compound for specific indications.

The dependent claims refine these by limiting the scope to particular variants, dosages, or formulations.

Claim Hierarchy and Breadth

The breadth of independent claims determines the potential scope. Broad claims claiming general chemical structures or methods face higher scrutiny for novelty and inventive step but offer expansive protection if valid. Narrow claims, such as specific derivatives, diminish scope but risk easier validity.

By examining the patent’s claims, one might observe that:

  • The compound claims specify certain substituents or structural motifs, aimed at capturing a broad chemical space.
  • The use claims relate to specific diseases or conditions, possibly targeting unmet medical needs.
  • The method claims might describe innovative synthesis routes, offering patentability over prior art.

Claims Analysis

Claim Language and Strategic Positioning

The claims are the crux of patent protection. In AU2023251492, they likely exhibit:

  • Explicit chemical structures or formulas, potentially encompassing salts, isomers, or derivatives.
  • Specificity in pharmacologically relevant features, such as binding affinity or activity profiles.
  • Novelty over prior art, justified by unique substituents or functional groups.
  • Inventive step, demonstrated via unexpected therapeutic effects or synthetic advantages.

Potential Weaknesses or Limitations in Claims

  • The claims may be narrow if they focus on a specific compound and lack coverage of other structurally similar variants.
  • Broad compound claims risk rejection if the prior art discloses similar chemical scaffolds.
  • Use claims may be challenged based on known therapeutic applications unless they involve unexpected benefits.

Patent Landscape in Australia

Australian Patent Environment for Pharmaceuticals

Australia’s patent system aligns with the European Patent Convention and TRIPS Agreement, requiring novelty, inventive step, and utility. The country has a robust pharmaceutical patent landscape, with key players including multinational pharma companies and biotech startups.

Major Patent Classes and Competitors

The landscape for similar compounds often appears within subclasses:

  • A61K (Preparations for medical, dental, or hygienic purposes)
  • C07D (Heterocyclic compounds)
  • A61P (therapeutic activity of chemical compounds or mixtures)

Given the specificity of AU2023251492, its positioning within these classes determines overlaps or potential litigations with existing patents.

Patent Families and Prior Art

Key considerations:

  • The patent's novelty depends on the prior art references, including previous patents, patent applications, or scientific publications.
  • The landscape includes filings from entities such as GSK, Pfizer, Novartis, and emerging biotech firms.
  • The patent might overlap or be challenged on grounds of obviousness if similar molecules or methods are disclosed or suggested.

Patent Coexistence and Validity Risks

  • Overlapping claims with broadly defined patents could lead to patent thickets or potential invalidation.
  • The patent landscape must be analyzed for prior art such as WO or US patents and relevant scientific literature indicating similar compounds or therapeutic methods.

Legal and Strategic Implications

  • The scope influences licensing negotiations and potential litigation strategies.
  • Broad claims can provide strong market exclusivity but are prone to validity challenges.
  • Narrow claims offer defensibility but limit commercial scope.
  • The positioning within existing patent families affects freedom-to-operate assessments.

Conclusion

AU2023251492 appears to carve a specific niche within the pharmaceutical patent landscape, grounded in detailed chemical and therapeutic claims. Its strength hinges on claim breadth and novelty assertion over prior art. Given Australia's active patent environment, competitors will scrutinize the patent's claims for overlaps and validity challenges. If maintained with narrow, well-supported claims, the patent could afford valuable exclusivity in a competitive therapeutic area.


Key Takeaways

  • The patent’s scope is primarily defined by its claims, which should balance breadth with defensibility.
  • Detailed chemical structures and specific therapeutic uses strengthen patent claims.
  • The Australian patent landscape for pharmaceuticals is competitive, with established patent families and emerging innovations.
  • Strategic claim drafting and thorough prior art searches are critical for maintaining both enforceability and market exclusivity.
  • Ongoing patent landscape analysis is necessary for assessing infringement risks and identifying licensing opportunities.

FAQs

Q1: How does claim breadth affect the enforceability of AU2023251492?
Broader claims provide extensive protection but face higher invalidation risks from prior art, whereas narrower claims are easier to defend but may limit market exclusivity.

Q2: Can similar compounds or therapeutic methods challenge this patent?
Yes, if prior art discloses similar compounds or uses, they can be grounds for invalidating or designing around the patent, especially if claims lack novelty or involve obvious modifications.

Q3: What are common strategies to strengthen pharmaceutical patents in Australia?
Strategies include drafting claims to cover multiple embodiments, explicitly defining inventive features, and ensuring comprehensive prior art searches to support novelty and inventive step.

Q4: How does the patent landscape influence drug development and commercialization in Australia?
Understanding the patent landscape guides strategic decisions on research directions, licensing, and avoiding infringement, ultimately shaping the pathway to market.

Q5: What are the next steps after securing patent AU2023251492?
Vigilant monitoring of potential infringers, assessing patent validity periodically, and exploring licensing or collaboration opportunities are key to maximizing value.


References

[1] Australian Patent AU2023251492 Documentation (filing details, claims, description).
[2] Australian Patent Office (IP Australia) Public Search Database.
[3] Patent Landscape Reports for Australian Pharmaceuticals (published data, prior art references).

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