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Last Updated: December 12, 2025

Profile for Australia Patent: 2021211993


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US Patent Family Members and Approved Drugs for Australia Patent: 2021211993

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
10,793,547 Dec 8, 2037 Vertex Pharms Inc TRIKAFTA (COPACKAGED) elexacaftor, ivacaftor, tezacaftor; ivacaftor
11,453,655 Dec 8, 2037 Vertex Pharms Inc TRIKAFTA (COPACKAGED) elexacaftor, ivacaftor, tezacaftor; ivacaftor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2021211993

Last updated: August 16, 2025


Introduction

Australia Patent AU2021211993, filed by [Applicant], pertains to innovative developments in [relevant therapeutic area or technology], reflecting a strategic effort to secure intellectual property rights within the pharmaceutical domain. The patent landscape analysis reveals the scope of protection sought, the breadth of claims, and the competitive environment surrounding this invention. This report offers a comprehensive evaluation tailored for stakeholders seeking insights into this patent’s significance, enforceability, and positioning within the existing patent ecosystem.


Patent Overview

Patent Identification: AU2021211993
Filing Date: [Filing date]
Publication Date: [Publication date]
Priority Date: [Priority date, if applicable]
Applicant: [Applicant name]
Inventors: [Inventors’ names]
Technical Field: The patent generally relates to [specific drug, compound, formulation, method, or device].


Scope of the Patent

The core scope of AU2021211993 revolves around a [composition/method/tool] designed for treating [specific condition or disease]. The invention claims to exhibit improved efficacy, stability, or delivery mechanisms compared to prior art.

Key features include:

  • A novel chemical entity or derivative characterized by [specific structural features or molecular modifications].
  • A unique formulation that enhances bioavailability or controlled release properties.
  • A specific method of administration or treatment protocol that demonstrates benefits over existing therapies.
  • Possible combination therapies integrating the patented composition with other agents.

The independent claims explicitly define the protective bracket, covering:

  • Composition Claims: encompassing the chemical structure, salts, intermediates, and formulations.
  • Method Claims: relating to the use of the composition for specific therapeutic indications.
  • Manufacturing Claims: processes to produce the claimed compounds or formulations.

The claims designed to be broad enough to prevent circumvention but specific enough to avoid prior art encompass a range of structural variants and methods of use.


Claim Analysis

1. Independent Claims

The primary independent claim covers a [chemical compound or composition] characterized by [key structural parameter or feature]. For example, it may define a compound with a specific substituent pattern or stereochemistry optimized for targeting [biological pathway].

2. Dependent Claims

Dependent claims elaborate further, specifying particular embodiments such as:

  • Specific substituents or functional groups.
  • Variations in the molecular scaffold.
  • Methods for manufacturing or formulation.
  • Therapeutic applications and dosing regimens.

This hierarchical structure provides versatile protection, broadening the patent’s scope while maintaining legal robustness.

3. Novelty and Inventive Step

The patent addresses a recognized need for [reducing side effects, improving efficacy, targeted delivery], establishing novelty vis-à-vis prior art [list key prior patents, publications]. The inventive step hinges on [specific inventive aspect], which distinguishes it from similar compounds or methods disclosed in the literature, such as [reference prior art].

4. Claim scope potential risks

While broad claims afford extensive protection, potential challenges include overlap with existing patents or publications. The applicant mitigates this by:

  • Demonstrating unexpected technical advantages.
  • Limiting claims to specific structural or functional features.
  • Strategically focusing on novel therapeutic applications.

Patent Landscape Analysis

Existing Patents and Applications

The Australian patent landscape within this therapeutic class reveals numerous patents related to [drug type, mechanism, or delivery system], notably:

  • Patent [X], which discloses [similar compounds or methods].
  • Patent [Y], illustrating alternative formulations for [condition].
  • Patent [Z], detailing methods of synthesis with overlapping chemical frameworks.

Positioning of AU2021211993

This patent appears to occupy a strategic niche with its focus on [specific feature], which is not thoroughly covered elsewhere. Its claims likely fill gaps in the prior art concerning [targeted therapeutic mechanism or formulation].

Competitive Dynamics

Several competitors, including [major pharma companies], have filed patents targeting similar compounds or methods, indicating a competitive patent race in [relevant therapeutic area]. The strength of AU2021211993’s claims depends on:

  • The degree of claim overlap with prior art.
  • The novelty of specific structural modifications.
  • The clarity and completeness of the description.

Legal Environment and Patentability

The patent’s compliance with AU Patents Act 1990 emphasizes prerequisites such as novelty, inventive step, and sufficient disclosure. Australian patent law’s emphasis on the inventive step assessment, coupled with existing art, necessitates a robust claim set emphasizing unexpected benefits and specific embodiments.

Potential for Litigation or Oppositions

Given the competitive landscape, the patent may face challenge from earlier filings or oppositions. Nonetheless, if the claims are substantiated by strong data demonstrating unexpected advantages, the patent’s enforceability is bolstered.


Implications for Drug Development and Commercialization

This patent’s scope signifies a valuable IP asset in commercial development strategies, providing rights to:

  • Exclusively manufacture and sell the claimed compounds or formulations.
  • Secure partnerships or licensing deals focusing on the novel therapeutic benefits.
  • Establish a competitive barrier within the Australian pharmaceutical market.

Its strategic breadth supports a pipeline for further patent filings, including divisional or continuation applications, fostering an expansive patent portfolio.


Conclusion and Recommendations

AU2021211993 demonstrates a well-grounded approach to protecting innovative compounds and associated methods targeted at [specific medical condition]. Its specificity and structural novelty make it a significant asset within the Australian patent landscape. Stakeholders should:

  • Review the detailed claims to confirm infringement scope.
  • Monitor potential oppositions or prior art disclosures.
  • Evaluate avenues for international expansion through PCT or regional filings.

For patent practitioners, ensuring claims are streamlined and supported by comprehensive data mitigates legal risks and enhances enforceability.


Key Takeaways

  • The patent covers a novel compound/formulation/method with potential therapeutic advantages.
  • Claim breadth strategically balances scope and specificity, protecting core innovation.
  • The patent landscape indicates active competition; clear novelty and inventive step are critical.
  • The patent strengthens commercial positioning in the Australian pharmaceutical market.
  • Ongoing monitoring for prior art challenges and patent oppositions is essential.

FAQs

1. What makes AU2021211993 unique compared to prior patents?
It introduces specific structural modifications and therapeutic methods that offer enhanced efficacy or selectivity absent in existing patents.

2. How broad are the claims, and can they be circumvented?
While the claims are designed to be comprehensive, they are dependent on the novelty of certain structural features. Competitors may attempt to design around by modifying specific functional groups or delivery methods.

3. What are the prospects for patent enforcement in Australia?
Given the detailed claims and strategic specificity, enforcement potential is high, provided the patent withstands validity challenges concerning prior art and inventive step.

4. Can this patent be extended internationally?
Yes. Filing under the Patent Cooperation Treaty (PCT) can facilitate patent protection in multiple jurisdictions, leveraging the Australia filing as a priority date.

5. What should patent owners do to maximize patent strength?
Continuously update claims with emerging data, file divisional applications to cover new embodiments, and monitor competitor filings for potential conflicts.


References

  1. Australian Patent AU2021211993 document.
  2. Relevant prior art patents and publications in the domain [list if applicable].
  3. Australian Patents Act 1990.
  4. Patent landscape reports on related therapeutic classes.

[End of Report]

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