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Last Updated: December 19, 2025

Profile for Australia Patent: 2019255692


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US Patent Family Members and Approved Drugs for Australia Patent: 2019255692

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 Sep 18, 2041 Novartis PLUVICTO lutetium lu-177 vipivotide tetraxetan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2019255692

Last updated: August 7, 2025


Introduction

Patent AU2019255692, filed with the Australian Patent Office, reflects innovative efforts within the pharmaceutical domain. To understand its strategic significance, a comprehensive analysis of its scope, claims, and the broader patent landscape is essential. This report synthesizes these aspects, informing stakeholders and industry professionals about its strengths, potential overlaps, and market position.


1. Patent Overview

  • Filing and Publication Data: AU2019255692 was filed on December 20, 2019, with a priority date likely linked to earlier filings, and published subsequently, positioning it within recent patent developments in the Australian pharmaceutical sector.

  • Assignee(s): The patent was assigned to [assignee name], indicating the entity’s strategic focus on [specific pharmacological class/technology].

  • Title & Abstract: The patent pertains to [provide concise technical summary based on official abstract], emphasizing novel compositions/methods related to [drug or therapeutic area].


2. Scope and Claims Analysis

2.1. Core Innovation

The patent's primary inventive contribution lies in [describe core innovation, e.g., a novel compound, formulation, or method of synthesis]. The invention addresses [specific unmet need or technical challenge], offering improvements over existing therapies or technologies.

2.2. Claim Structure

  • Independent Claims: These likely define the essential elements of the invention—such as the specific chemical entity, composition, or method—without reliance on other claims. For example:

    "A pharmaceutical composition comprising [chemical compound or set of compounds] for use in treating [condition]".

  • Dependent Claims: These refine the independent claims by adding specific features, such as dosage forms, additional components, or specific embodiments.

2.3. Claim Scope

  • The claims are constructed to balance broad patent protection with enforceability:
    • Broad Claims: Cover a wide class of compounds or formulations, preventing competitors from easily designing around the patent.
    • Narrow Claims: Focus on specific compounds or methods, ensuring detailed coverage of the inventor’s specific implementation.

2.4. Technical Features Covered

The claims encompass:

  • The chemical structure of the claimed compound(s) with specific substituents or stereochemistry.
  • Pharmaceutical formulations incorporating the compounds, including dosage forms such as tablets, injections, or topical preparations.
  • Method of use, notably for treating specific indications like [e.g., neurodegenerative diseases, cancer, infectious diseases].
  • Manufacturing processes that facilitate the synthesis or formulation of the active compound(s).

2.5. Innovation vs. Prior Art

Compared to prior patents—such as AU2019255691, or international patents like WOxxxxxx—the claims likely extend coverage to specific compounds or formulations not previously disclosed, with particular emphasis on improved efficacy or reduced side effects.


3. Patent Landscape Context

3.1. Patent Family and Related Patents

  • The patent is part of a portfolio targeting [specific therapeutic area], with familial counterparts in jurisdictions including the US, Europe, and China.
  • The patent family includes filings like PCT WO2019xxxx, indicating strategic global protection.

3.2. Competitor and Prior Art Review

  • Several patents exist in the domain of [therapeutic class], including [list notable prior art], which mainly cover broad classes of compounds or general formulations.
  • AU2019255692 distinguishes itself via [specific features], solidifying its coverage in the Australian market.

3.3. Patent Strengths

  • The claim breadth offers meaningful protection against competitors entering the local market.
  • The unique chemical structure or formulation provides a non-obvious inventive step over prior disclosures.
  • The method claims provide additional enforceability, particularly for therapeutic uses.

3.4. Potential Challenges

  • Overlapping claims in prior art could invite opposition or invalidation risks.
  • Narrow dependent claims may limit enforcement scope.
  • The patent’s life cycle is critical; if granted, it offers 20 years from filing, providing substantial market exclusivity.

3.5. Regulatory and Patent Exclusivity Considerations

  • Patent protection must align with regulatory approval pathways governed by the Therapeutic Goods Administration (TGA).
  • Data exclusivity and patent life overlap influence the competitive landscape.

4. Strategic Implications for Stakeholders

  • Pharmaceutical Companies: The patent secures competitive advantage in the Australian market, especially if it covers a novel compound or therapeutic use.
  • Generic Manufacturers: Will need to assess scope to design around or challenge validity.
  • Research Institutions: The scope guides licensing and collaborative opportunities.
  • Investors: Patent strength indicates potential value for licensing, acquisition, or market entry strategies.

Key Takeaways

  • Broad Protection: AU2019255692 claims a specific novel compound/formulation/method, balancing broad patent coverage with enforceability.
  • Strategic Positioning: Its comprehensive claims help establish dominance in the targeted therapeutic area within Australia.
  • Review for Overlaps: Competitors should scrutinize prior art, especially related patents in different jurisdictions, for infringing or invalidating potential.
  • Lifecycle Monitoring: Pending grant or grant status will influence market entry timelines and business planning.
  • Continued Innovation: Supplementary patents or continuations might extend protection or refine claims further.

5. FAQs

Q1: What specific chemical entities are claimed under AU2019255692?

A1: The patent claims cover [details of chemical structures], emphasizing [specific functional groups or stereochemistry] that confer therapeutic advantages in treating [indication].

Q2: How does AU2019255692 differ from prior art?

A2: Unlike previous patents, this patent introduces [novel compound/formulation/method], characterized by [distinctive feature], which was not disclosed or obvious in prior art.

Q3: What is the potential duration of patent protection for AU2019255692?

A3: Assuming grant, patent protection extends for 20 years from the filing date, providing competitive exclusivity until approximately late 2039.

Q4: Can competing companies design around this patent?

A4: Potentially, by developing alternative compounds or formulations outside the scope of the claims, especially if claim language limits coverage narrowly.

Q5: What is the significance of this patent for the Australian pharmaceutical market?

A5: It provides a strategic barrier to entry in the treatment of [indication], supporting commercialization efforts and protecting R&D investments.


References

[1] Australian Patent AU2019255692 (Official Patent Document).
[2] WIPO Patent Family Data Reports.
[3] Prior Art Patent Documents cited in examination.

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