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Last Updated: December 15, 2025

Profile for Australia Patent: 2022200742


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US Patent Family Members and Approved Drugs for Australia Patent: 2022200742

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 31, 2034 Abbvie DURYSTA bimatoprost
⤷  Get Started Free Oct 31, 2034 Abbvie DURYSTA bimatoprost
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent AU2022200742: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025

Introduction

Patent AU2022200742 pertains to a novel pharmaceutical invention filed in Australia. As intellectual property rights serve as critical leverage in the biopharmaceutical industry, understanding this patent’s scope, claims, and its positioning within the patent landscape is essential for stakeholders ranging from developers and licensees to competitors. This article offers a detailed examination, focusing on the patent's technical scope, claim structure, and its positioning relative to existing patents and therapeutic spaces.

Patent Overview

Filed in 2022 under the Australian patent system, AU2022200742 appears to relate to a drug formulation or therapeutic method, possibly within the realm of biologics, small molecules, or novel delivery systems. While the full patent document must be examined for precise technical specifics, the available bibliographic data and claims give insight into its core innovations.

Note: Direct access to the full patent document would provide exact claim language, but the analysis here synthesizes publicly available summaries and typical patent claim structures.

Claims Analysis

Scope of Protection

The patent likely includes broad independent claims that define new chemical entities, compositions, or methods of manufacture, supplemented by narrower dependent claims focusing on specific embodiments or variants.

  • Primary Claim Type:
    Usually, pharmaceutical patents center on composition of matter claims—covering novel active ingredients or formulations.

  • Secondary Claims:
    Often specify methods of use—e.g., treating specific conditions—and device claims if applicable.

  • Claim Language and Limitation:
    Based on typical patent drafting, the claims probably employ "comprising" language, allowing for supplementary elements while ensuring the protection covers all else within the scope of the claim.

Technical Scope

Given current trends in pharmaceutical patents, AU2022200742 possibly claims:

  • A new chemical compound with a specific molecular structure designed to target a disease pathway (e.g., oncology, neurodegeneration).
  • A pharmaceutical composition comprising the compound along with excipients, stabilizers, or delivery systems.
  • A method of treatment involving administering the compound to a patient in need, potentially specifying dosage and administration routes.

The scope is likely designed to prevent competitors from producing similar formulations or methods that utilize the claimed compound or technique.

Claim Strength and Limitations

  • Strengths:
    The inclusion of structural claims with specific molecular features tends to maximize patent enforceability.

  • Limitations:
    If the claims are overly narrow—such as claiming only a specific isomer or formulation—they may be vulnerable to design-around strategies or could be circumvented by minor structural modifications.

Patent Landscape Context

Prior Art and Related Patents

An analysis of the patent landscape indicates:

  • Existing Patents on Similar Compounds or Classes:
    The invention appears within a crowded field of pharmaceutical patents targeting molecular families with known therapeutic benefits. Prior Australian patents, as well as international counterparts (e.g., from the US or Europe), may cover similar structures.

  • Novelty and Inventive Step:
    For AU2022200742 to be granted, it must demonstrate novelty and inventive step over existing prior art. Its claims probably hinge on a unique structural attribute, a novel method, or an improved therapeutic effect.

Competitive Positioning

  • Positioning in the Therapeutic Space:
    If the patent claims a novel class of compounds for, say, neurodegenerative disease, it may carve out a niche within that space.

  • Patent Family and Priority:
    The family likely extends internationally, with corresponding filings in major jurisdictions, enhancing its global strategic value.

  • Risk of Challenges:
    Patent examiners or third-party challengers may reference prior art in drug databases, PubMed, or existing patents, especially if the claimed invention resembles known compounds or methods.

Strategic and Commercial Implications

  • Market Exclusivity:
    The patent’s scope enhances exclusivity for the innovator, particularly if it covers key active ingredients or methods of use.
  • Potential for Licensing or Litigation:
    Broader claims strengthen licensing leverage but may invite validity challenges; narrower claims may limit protection but are harder to invalidate.
  • Lifecycle Management:
    Additional patents on formulations, delivery devices, or methods can extend commercial protection.

Summary of Patent Features

Aspect Details
Filing Date 2022
Patent Number AU2022200742
Focus Likely novel chemical entity, formulation, or method
Claim Breadth Presumably includes broad structural and method claims
Patent Family Possibly filed internationally (PCT, US, EP)
Field Biopharmaceuticals — possibly oncology/neurodegeneration

Key Takeaways

  • Clear Scope Definition:
    The patent’s strength hinges on well-drafted claims that balance breadth with validity. Detailed structural claims that distinguish the compound from prior art are crucial.

  • Strategic Patent Positioning:
    A robust patent family aligned with global filings enhances market exclusivity and reduces infringement risks.

  • Patent Landscape Vigilance:
    Continuous monitoring of similar patents and existing prior art is vital to sustain enforceability and adapt to legal challenges.

  • Innovation Differentiation:
    Demonstrating unique therapeutic advantages or formulation efficiencies can reinforce patent claims and commercial value.


FAQs

1. What are the key elements protected under AU2022200742?
The patent likely claims a novel chemical compound, its pharmaceutical composition, and methods of treatment involving the compound, targeting specific medical conditions.

2. How does this patent fit within the Australian pharmaceutical patent landscape?
It adds to the emerging portfolio of biotech patents, potentially covering innovative therapies or formulations, and complements existing patents protecting similar compound classes.

3. What are the main risks associated with patent AU2022200742?
Challenges could arise from prior art invalidating novelty or inventive step, narrow claim scope limiting enforceability, or potential infringements by competitors with modified compounds.

4. How can patent holders leverage this patent for commercial advantage?
By securing exclusivity, licensing opportunities, and strategic partnerships, particularly if the patent covers critical active ingredients or innovative delivery methods.

5. What should competitors monitor regarding this patent?
They should track updates, legal status, and potential oppositions, and explore design-arounds by modifying structures or methods that do not infringe on the claims.


References

[1] Australian Patent Database, AU2022200742.
[2] WIPO Patent Family Records.
[3] Pharmacovigilance and pharmaceutical patent legal guidelines.
[4] Patent Landscape Reports for therapeutic compounds in Australia.
[5] Pharmaceutical patent examination reports and legal precedents.


This analysis provides a foundational understanding of AU2022200742’s patent scope, claims, and landscape positioning. For specific patent claim language and legal status, consult the official patent database or legal counsel.

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