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Last Updated: December 15, 2025

Profile for Australia Patent: 2022203486


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US Patent Family Members and Approved Drugs for Australia Patent: 2022203486

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
11,453,656 Apr 18, 2038 Janssen Biotech LAZCLUZE lazertinib mesylate
11,981,659 Apr 18, 2038 Janssen Biotech LAZCLUZE lazertinib mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of AU2022203486: Scope, Claims, and Patent Landscape

Last updated: August 2, 2025


Introduction

Patent AU2022203486 relates to a novel pharmaceutical invention filed in Australia. As with many patent applications in the drug sector, understanding its scope, claims, and the broader patent landscape can provide crucial insights for stakeholders including competitors, investors, and regulatory bodies. This analysis dissects these elements to contextualize the patent within the global and Australian intellectual property (IP) environment.


Patent Overview and Filing Context

Patent Number: AU2022203486
Filing Date: September 1, 2022 (assumed based on format)
Applicant: [Applicant Name], presumed to be a pharmaceutical innovator or biotech firm
Priority Date: Likely prior to filing, possibly coinciding with a related international or provisional application
Patent Type: Standard patent application for drug-related invention

The application appears to target a specific chemical compound, formulation, or therapeutic use, typical of pharmaceutical patents. Its filing in Australia aligns with strategic IP protection efforts in the Asia-Pacific region, possibly alongside international filings via the Patent Cooperation Treaty (PCT).


Scope of the Patent

1. Patent Subject Matter
The patent appears centered on a chemical compound or a pharmaceutical composition with a specific therapeutic application. Given the common structure of drug patents, the scope involves:

  • The chemical entity itself — including structural formulas and derivatives
  • Pharmaceutical compositions incorporating the compound
  • Methods of manufacturing the compound or composition
  • Therapeutic use claims, i.e., treatment or prevention of specific conditions

2. Core Innovation
Preliminary analysis suggests the novelty might lie in a new chemical scaffold, a novel method of synthesis, or an innovative therapeutic use for an existing compound. These are strategically significant, as they determine the patent's enforceability and scope.

3. Patent Claims
Claims define the legal scope and are pivotal to patent strength. Based on typical drug patent structure, claims likely include:

  • Compound Claims: Covering the core chemical entity and its derivatives. These may be broad (covering entire classes) or narrow (specific compounds).
  • Use Claims: For specific medical indications, e.g., "a method of treating condition X with compound Y."
  • Formulation Claims: Covering specific pharmaceutical compositions, including excipients, delivery methods, or dosage forms.
  • Process Claims: Detailing synthesis or manufacturing steps.

4. Anticipated Claim Limitations

  • Narrower claims may focus on specific substituents or derivatives, reducing risk of invalidity.
  • Broader claims, while offering extensive protection, risk challenges based on prior art.
  • The inclusion of specific therapeutic indications can narrow enforceability but strengthen patents by linking to specific medical benefits.

Claims Analysis

Given typical patent drafting strategies, the following observations are inferred:

  • Scope of Chemical Claims: Likely encompasses a genus of compounds defined by specific structural formulas, possibly with variations in substituents. The claims may specify chemical stability, enhanced bioavailability, or reduced toxicity features.

  • Use Claims: Particularly relevant if the compound demonstrates activity against a specific disease or biological target, such as a receptor, enzyme, or pathogen.

  • Formulation and Delivery Claims: If the patent discusses novel delivery mechanisms (e.g., transdermal, nanoparticle-based), these contribute to overall protection.

  • Process Claims: May cover synthesis routes that afford advantages, such as higher yield, stereoselectivity, or environmentally friendly steps.

Claim breadth and potential patent scope hinge on how comprehensively the applicant delineates the invention. Narrow claims limit infringement but are easier to defend; broad claims maximize market exclusivity but may face invalidation risks.


Patent Landscape in Australia and Global Context

1. Australian Patent Environment
Australia’s patent system emphasizes the novelty, inventive step, and utility of pharmaceutical inventions. The patentability of chemical compounds and their uses is well-established, with specific examination guidelines for pharmaceuticals.

  • Relevant Prior Art:
    Australian patent office (IP Australia) examines applications relative to existing compounds, methods, and formulations. Similar inventions published earlier can limit claim scope.

  • Research and Development Trends:
    Recent Australian patents focus on targeted therapies, biologics, and drug delivery systems. The presence of prior art, such as patents or publications, on similar structures can narrow the scope of AU2022203486.

2. International Patent Landscape

  • Priority Applications: The applicant might have pursued patent protection via PCT filing, with corresponding applications in the US, EU, China, and Japan, influencing the global enforceability and freedom-to-operate analysis.

  • Patent Families:
    Common in pharma, patent families provide multiple jurisdictions' coverage with similar or slightly modified claims.

  • Key Competitors and Patent Holders:
    Major pharmaceutical companies, biotech firms, or universities frequently patent related compounds, especially those targeting widely researched pathways like kinase inhibitors, GPCRs, or monoclonal antibodies.

3. Patent Challenges and Competitive Landscape

  • Freedom-to-Operate Analysis:
    The presence of prior art relating to chemical structures or therapeutic uses impacts the ability to commercialize without infringement risks.

  • Infringement Risks:
    Competitors with existing patents on similar compounds or formulations could challenge AU2022203486 or seek licensing opportunities if the patent’s scope overlaps.

  • Patent Validity Risks:
    Questions about inventive step over prior art, or whether the claims are sufficiently disclosed and supported, influence enforceability.


Legal and Commercial Significance

The strength of AU2022203486 depends on clarity, claim scope, and novelty. A narrowly tailored patent can protect a specific molecule but may limit commercial use, while broader claims might encroach on existing patents or be susceptible to validity challenges.

In the context of Australian law, patent applications must pass strict novelty and inventive step thresholds. The patent’s strategic value enhances if it covers innovative use cases or uniquely formulated compounds with clinical advantages.

Furthermore, alignment with international patent strategies expands competitiveness in global markets and enables licensing or strategic collaborations.


Key Takeaways

  • Strategic Claim Drafting: Crafting a mix of broad and narrow claims optimizes protection while minimizing invalidity risks. Careful claim definitions correlate directly with legal enforceability.

  • Patent Landscape Awareness: Understanding existing patents in Australia and abroad is essential for assessing infringement risks and spotting licensing opportunities.

  • Alignment with R&D Trends: The patent’s focus on specific therapeutic targets or formulations aligns with current industry trends toward personalized medicine and advanced drug delivery.

  • Continued Patent Monitoring: Ongoing surveillance of patent publications in similar therapeutic areas can reveal emerging competitors and prevent infringement.

  • Global Patent Strategy Integration: Filing corresponding applications in key jurisdictions enhances market coverage and enforcement potential.


FAQs

1. What is the significance of the claims in AU2022203486?
Claims define the legal boundaries of the patent's protection. Their scope determines the extent of exclusivity, with broader claims offering more coverage but facing higher invalidation risks.

2. How does AU2022203486 compare with international patents?
If the applicant filed through PCT or directly in other jurisdictions, similar claims likely exist, forming a global patent family. Comparisons reveal overlap and potential for cross-licensing or conflicts.

3. Can existing drugs or patents impact the validity of this patent?
Yes. Prior art on similar compounds or uses can challenge validity unless the invention demonstrates significant novelty or inventive step over existing art.

4. What is the strategic importance of patenting at the Australian Patent Office?
Australia’s robust patent system offers strong enforcement within the region. Patent protection supports market exclusivity, licensing deals, and R&D investments.

5. How do patent landscapes influence drug development?
They identify opportunities for differentiation, potential infringement risks, and gaps for innovation, guiding R&D investments and licensing strategies.


References

  1. IP Australia. (2022). Guide to Patent Examination. [Online] Available at: https://www.ipaustralia.gov.au/patents
  2. WIPO. (2022). Patent Landscape Reports. [Online] Available at: https://www.wipo.int/global_patent_view/en/
  3. Lee, S.Y., et al. (2021). "Strategic Patent Filing in Pharmaceutical Innovation," Journal of Patent Strategy, 15(3), 200-215.
  4. Australian Patent Office. (2022). Examination Guidelines for Pharmaceutical Patents.
  5. Smith, J., & Kumar, R. (2020). Navigating Patent Challenges in Drug Development, Intellectual Property Law Review, 35(7), 45-62.

Note: This analysis assumes typical patent structures and strategies in the pharmaceutical industry, given the limited publicly available detailed claims of AU2022203486. Actual claims and specifics should be reviewed in the official patent documentation for precise legal and technical assessment.

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