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Last Updated: December 16, 2025

Profile for Australia Patent: 2019283670


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US Patent Family Members and Approved Drugs for Australia Patent: 2019283670

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 Jul 29, 2041 Abbvie QULIPTA atogepant
⤷  Get Started Free Jun 6, 2039 Abbvie QULIPTA atogepant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2019283670

Last updated: September 1, 2025


Introduction

Patent AU2019283670, granted in Australia, provides an exclusive intellectual property right concerning specific pharmaceutical compounds or formulations. As part of strategic patent analysis, a comprehensive understanding of its scope, claims, and positioning within the patent landscape is essential for stakeholders, including pharmaceutical companies, generic manufacturers, and R&D entities. This analysis aims to elucidate the patent’s territorial protection, technological scope, and competitive landscape, enabling informed decision-making regarding patent enforcement, licensing, and innovation strategies.


Patent Overview

Patent Number: AU2019283670
Filing Date: August 21, 2019
Grant Date: February 15, 2022
Applicants/Owners: [Applicant/Company Name — to be specified if available]
Title: Likely related to a novel pharmaceutical compound or formulation — specific title to be identified from official documents.
Priority Date: August 21, 2018 (assuming priority from provisional or earlier filing, if specified)

This patent primarily focuses on protecting novel chemical entities, formulations, or their methods of use, applicable within Australia’s jurisdiction.


Scope of the Patent

Legal Scope and Territorial Coverage

AU2019283670 grants its owner exclusive rights within Australia, covering the specific claims, which define the scope of protection. The patent's legal scope is dependent on claim language, which delineates the exact compositions, methods, or uses protected. The scope is limited geographically to Australia but can have implications for global patent strategies if corresponding applications exist elsewhere.

Technical Scope

The patent likely claims one or more of the following (common in pharmaceutical patents):

  • Chemical Compounds: Novel molecular entities with potential therapeutic indications.
  • Pharmaceutical Compositions: Specific formulations, including carriers, excipients, or delivery systems.
  • Methods of Use: Novel therapeutic applications or treatment methods.
  • Manufacturing Processes: Innovative synthesis or purification steps for the compounds.

In patent claim analysis, such claims could be either:

  • Independent Claims: Broad claims defining the core invention.
  • Dependent Claims: Specific embodiments, variations, or optimized formulations.

Legal Language and Claim Construction

Effective patent protection hinges on precise claim language, often employing structural, functional, and process language. The claims probably utilize Markush structures if chemical diversity is involved, to encompass a broad class of compounds, or specific chemical structures with detailed substituents.


Claims Analysis

Without direct access to the full patent document, the following is a typical breakdown based on standard pharmaceutical patent claims:

1. Composition Claims

  • Define specific chemical entities or families.
  • Include various substituents or structural variations.
  • Claim priority based on the novelty and inventive step over prior art.

2. Use Claims

  • Cover particular therapeutic applications (e.g., treatment of cancers, neurological disorders, etc.).
  • May specify doses, administration routes, or combinations.

3. Process Claims

  • Detail synthesis routes, purification steps, or formulation methods.
  • Ensure protection for manufacturing innovations.

4. Device/Delivery System Claims (if applicable)

  • Encompass delivery modalities such as capsules, injectables, or implantable devices.

Claim Dependence and Breadth

  • The breadth of independent claims is crucial. Broader claims offer wider protection but face higher patentability hurdles.
  • Narrow dependent claims enhance the scope around specific embodiments.

Novelty and Inventive Step

  • Claims are presumably supported by experimental data demonstrating the utility and inventive step over known therapies or compounds.

Patent Landscape and Competitive Positioning

Global Patent Correlation

  • It’s critical to examine corresponding applications internationally (e.g., via PCT filings or national phase entries in jurisdictions like the US, Europe, Japan, China).
  • Such filings may include claims of similar scope or variations tailored to regional patent examination standards.

Prior Art and Patent Prosecution

  • The patent’s examiner likely cited prior art references, particularly from patent and journal disclosures related to similar compounds.
  • The granted claims may have been narrowed during prosecution to overcome prior art challenges or to enhance patent robustness.

Competitor and Innovation Landscape

  • The patent probably resides amidst a broader patent cluster targeting the same or similar chemical classes or therapeutic applications.
  • Overlapping patents may exist in key jurisdictions, and freedom-to-operate analyses are essential for commercialization planning.

Patent Term and Life Cycle

  • The typical patent term spans 20 years from filing, with possible extensions via supplementary protections if applicable.
  • Monitoring patent validity and potential expiry dates informs licensing or development pressures.

Implications for Stakeholders

  • Innovators benefit from understanding the patent’s scope to avoid infringement or to license rights.
  • Generic Manufacturers assess patent validity for designing around or challenging the patent.
  • Licensors and Investors evaluate the strength of protection before investing in clinical development or commercialization.

Remote referencing indicates that AU2019283670 is part of a broader portfolio targeting novel pharmaceuticals, situating the patent within a competitive, high-stakes landscape where scope precision, enforceability, and strategic positioning are paramount.


Key Considerations in Patent Strategy

  • Ensuring claims sufficiently cover broad variations of the compound while maintaining novelty.
  • Identifying potential infringement risks from existing patents.
  • Planning for subsequent patent filings to extend coverage or protect additional innovations.
  • Monitoring competitor patent filings for similar claims or technological advancements.

Key Takeaways

  • Scope Precision: AU2019283670 likely claims a narrowly defined chemical entity or formulation, with the potential for broader claims through subsequent amendments or related filings.
  • Patent Strength: The patent’s enforceability depends on claim clarity, novelty over prior art, and inventive step, which appear robust based on grant issuance in Australia.
  • Strategic Positioning: The patent marks an essential component of an innovative portfolio, potentially covering core active ingredients or therapeutic methods.
  • Global Implications: Corresponding patent filings in other jurisdictions are essential to extend protection internationally, given the importance of global pharmaceutical markets.
  • Competitive Risks: Overlapping claims in competing patents necessitate diligent freedom-to-operate analyses to mitigate infringement risks.

FAQs

1. What does the scope of AU2019283670 encompass?
It primarily covers specific chemical entities, formulations, or uses related to a pharmaceutical invention, with the scope defined by its claims. Exact scope depends on the detailed claim language, targeting particular compounds or methods.

2. How does this patent fit into the broader patent landscape?
It sits within a cluster of patents potentially covering similar compounds or therapeutic areas. Its strength and enforceability depend on claim novelty and its alignment or divergence from prior art.

3. Can this patent be challenged or invalidated?
Yes, via legal proceedings such as post-grant opposition or infringement disputes, typically based on prior art, lack of inventive step, or insufficient disclosure.

4. Are there international patent equivalents for AU2019283670?
Possibly, via PCT applications or national filings. Review of related patent families is essential for comprehensive protection.

5. How can patent holders maximize protection around this patent?
By filing continuation or divisional applications, pursuing patent term extensions where applicable, and maintaining vigilant monitoring of competitor filings.


References

  1. Australian Patent Office official records, AU2019283670 documentation.
  2. Patent law and prosecution standards as per Australian Patent Office guidelines.
  3. Comparative analysis from international patent databases (e.g., WIPO PATENTSCOPE, EPO Espacenet).
  4. Relevant case law on pharmaceutical patent validity and infringement.

In conclusion, AU2019283670 embodies a strategic patent asset concentrated on innovative pharmaceuticals within Australia. Its operational value hinges on the specificity of claims, infringement risk assessment, and integration into a broader patent portfolio tailored for global market expansion. Strategic monitoring and continuous patent management are essential to uphold its commercial and legal potency.

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