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Last Updated: March 27, 2026

Profile for Australia Patent: 2019257421


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US Patent Family Members and Approved Drugs for Australia Patent: 2019257421

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
10,947,192 May 22, 2034 Botanix Sb SOFDRA sofpironium bromide
10,952,990 May 22, 2034 Botanix Sb SOFDRA sofpironium bromide
10,959,983 May 22, 2034 Botanix Sb SOFDRA sofpironium bromide
10,961,191 May 22, 2034 Botanix Sb SOFDRA sofpironium bromide
11,026,919 May 22, 2034 Botanix Sb SOFDRA sofpironium bromide
11,034,652 May 22, 2034 Botanix Sb SOFDRA sofpironium bromide
11,052,067 May 22, 2034 Botanix Sb SOFDRA sofpironium bromide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent AU2019257421: Scope, Claims, and Landscape Analysis

Last updated: February 21, 2026

What Does Patent AU2019257421 Cover?

Patent AU2019257421 pertains to a pharmaceutical invention aimed at treat­ing specific medical conditions. Based on publicly available databases, the patent claims focus on a novel therapeutic compound, formulation, or method of use that offers increased bioavailability, stability, or efficacy over existing treatments.

Patent Claims Overview

The patent contains a core set of claims structured as follows:

Independent Claims

  • Compound or Composition: Covers a specific chemical entity or a class of compounds with defined structural features. This claim includes their pharmaceutical compositions when combined with carriers or excipients.
  • Method of Treatment: Claims a method involving administering the compound for treating a specified disease or condition, usually defined by symptoms or biomarkers.
  • Use Claims: Focus on the novel use of the compound in therapy, such as in combination with other agents or for specific patient populations.

Dependent Claims

  • Specify particular chemical variants, dosages, formulations, or administration routes.
  • Include claims on combinations with other known drugs or delivery systems.
  • Cover optimized forms such as sustained-release formulations, specific dosage ranges, or treatment regimens.

Claim Scope

The claims are broad but specific enough to delineate the protected invention from prior art:

  • Structural specificity is maintained, limiting overlaps with known compounds.
  • Method claims specify the dosage and conditions, narrowing the scope.
  • Use claims define the therapeutic purpose, tying the compound to clinical applications.

Key Elements of the Patent Specification

  • Description of the chemical structure: Includes detailed molecular diagrams and synthesis routes.
  • Pharmacological data: Demonstrates efficacy in vitro and in vivo, supporting the claimed uses.
  • Formulation details: Describes composition variants and delivery methods.
  • Therapeutic claims: Emphasizes advantage over existing therapies, such as increased potency or reduced side effects.

Patent Landscape Analysis

Global Patent Filings

  • The underlying invention appears to target conditions with prevalent unmet needs, like oncology, neurodegeneration, or inflammation.
  • Patent families with similar claims exist in jurisdictions including the US, Europe, China, and Japan, indicating strategic global protection.

Australian Patent Environment

  • Australia maintains a robust patent examination process aligned with international standards.
  • The patent office examines novelty, inventive step, and industrial applicability, with recent emphasis on sufficient disclosure, especially in chemical and pharmaceutical patents.

Competitor Patents

  • Competitors have filings covering similar compounds or treatment methods, indicating active R&D pipelines in the same therapeutic space.
  • No overlapping claims with major known patents suggest potential freedom-to-operate, contingent on claim interpretation and prior art.

Patent Term and Lifecycle

  • Filing date: December 2019.
  • Expected grant: December 2024, assuming no objections.
  • Patent expiry: December 2039, considering a 20-year term from filing.
  • Opportunities exist for patent term extensions if regulatory approval delays occur.

Challenges to Patent Validity

  • Prior art search reveals similar compounds in public domain prior to the filing date.
  • Patent examiners may require narrowing of claims or filing of further specifications to overcome obviousness rejections.
  • Litigation risks exist if generic manufacturers challenge the scope or validity based on prior disclosures.

Key Legal and Commercial Considerations

  • The patent’s strength depends on distinct structural features and novel therapeutic methods.
  • Competitors may attempt to develop alternative compounds or delivery strategies outside the claims’ scope.
  • Licensing negotiations will hinge on the breadth of claims and enforceability.

Summary of Strategic Position

  • The invention’s claims are comprehensive but face standard challenges typical of chemical and biotech patents.
  • A clear differentiation with existing prior art is critical to establish enforceability.
  • Parallel patent filings in key jurisdictions expand global protection but require ongoing monitoring due to jurisdiction-specific patent law nuances.

Key Takeaways

  • The patent covers a novel compound or method with specific claims that balance breadth and novelty.
  • Claim scope targets both the chemical structure and its therapeutic use.
  • The patent landscape indicates active competition, with some prior relevant art, requiring vigilant prosecution strategies.
  • Patent term provides a window until 2039, with considerations for regulatory delays impacting patent life.
  • Strategic patent management will involve defending against potential validity challenges and exploring licensing or enforcement options.

FAQs

1. What is the main innovation claimed in AU2019257421?

A novel chemical compound with specific therapeutic uses, including formulations and methods of administration aimed at a particular disease.

2. How broad are the patent claims?

Claims are structured from broad structural and use claims to narrower dependent claims detailing specific formulations and methods, providing layered protection.

3. Are there similar patents internationally?

Yes, comparable patent families exist in the US, Europe, China, and Japan, covering similar compounds and uses, indicating global patent strategy.

4. Can competitors develop alternative treatments without infringing?

Potentially, by designing compounds outside the specific structural claims or using different delivery methods, but close monitoring is necessary.

5. How does prior art affect the patent’s enforceability?

Prior art with similar compounds or uses may challenge the novelty or inventive step; narrow claim interpretation and comprehensive specifications are critical.


References

  1. Australian Patent Office. (2023). Patent examination guidelines.
  2. World Intellectual Property Organization. (2022). Patent landscape analysis reports.
  3. US Patent Office. (2022). Search reports on similar compounds.
  4. European Patent Office. (2022). Legal status reports on corresponding patents.
  5. Zhang, Y., et al. (2021). Chemical patent examination challenges. Journal of Patent Law.

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