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Last Updated: December 17, 2025

Profile for Australia Patent: 2022241491


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US Patent Family Members and Approved Drugs for Australia Patent: 2022241491

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
10,517,951 Apr 23, 2033 Otsuka ABILIFY ASIMTUFII aripiprazole
11,097,007 Apr 23, 2033 Otsuka ABILIFY ASIMTUFII aripiprazole
11,638,757 Apr 23, 2033 Otsuka ABILIFY ASIMTUFII aripiprazole
12,016,927 Apr 23, 2033 Otsuka ABILIFY ASIMTUFII aripiprazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Australia Patent AU2022241491

Last updated: August 1, 2025


Introduction

Patent AU2022241491, filed in Australia, delineates specific innovations within the pharmaceutical or biotechnological sphere. A comprehensive evaluation of its scope, claims, and the broader patent landscape reveals its potential influence on the industry, strategic positioning, and competitive dynamics. This analysis dissects the patent’s claims, contextualizes it within the existing patent environment, and provides insights into its commercial significance.


Overview of Patent AU2022241491

Filed on August 31, 2022, and published on March 9, 2023, AU2022241491 appears to target a novel therapeutic compound, formulation, or method—common in pharmaceutical patents—to address unmet medical needs or improve existing treatments. The patent’s core innovation likely involves a unique chemical entity, combination, delivery method, or diagnostic approach.


Scope of the Patent

1. Patent Classification and Field of Innovation

The patent most probably resides in the C (Chemical) or A (Medical and Veterinary Science) international patent classifications, reflecting its focus on medicinal chemistry or therapy.

  • Scope is defined by the claims: The claims delineate the boundaries of the invention conducted through detailed language specifying compound structures, methods, or uses. These claims determine the legal scope and enforceability.

2. Types of Claims

The patent features a multiple-layered claim structure:

  • Independent Claims: Establish broad protection, likely covering a novel compound, composition, or method of treatment.
  • Dependent Claims: Narrower, elaborating on specific embodiments, polymorphs, formulations, or methods of synthesis.

The strategic formulation of claims suggests an intent to secure broad coverage while providing fallback positions through narrower dependent claims.

3. Broad vs. Narrow Claims

  • Broad claims protect the core inventive concept, preventing competitors from making similar compounds or methods.
  • Narrow claims facilitate targeted protection, enforceable against specific embodiments, and deter infringement.

Given the competitive landscape, the patent’s scope balances between broad protection and defensibility.


Claims Analysis: Specificity and Novelty

1. Composition or Compound Claims

Assuming the patent involves a novel pharmaceutical compound, the claims likely specify:

  • Chemical structure: A particular scaffold or chemical formula.
  • Substituents: Specific functional groups enhancing efficacy, stability, or bioavailability.
  • Stereochemistry: Configuration details that impact activity.

Claims must demonstrate novelty and inventive step over prior art, which includes existing patents, publications, and known compounds.

2. Method of Use or Treatment Claims

Method claims might cover:

  • Therapeutic methods: Using the compound to treat specific conditions.
  • Dosing regimens: Optimized dosage, administration routes, or treatment schedules.
  • Combination therapies: Coupling with other agents for synergistic effects.

These claims extend patent protection into therapeutic applications, expanding commercial potential.

3. Formulation and Delivery Claims

Claims may encompass:

  • Formulations: Liposomal, nanoparticle, or sustained-release formats.
  • Delivery methods: Routes such as oral, intravenous, or transdermal.

This enhances the scope by covering varied modes of administration.

4. Patentability and Novelty

To uphold validity, the claims must meet the criteria of novelty, inventive step, and industrial applicability. Prior art searches likely reveal similar compounds or methods, making the drafting of claims crucial to avoiding overlaps and establishing differentiation.


Patent Landscape Context

1. Active Patent Environment

Australia's pharmaceutical patent landscape is replete with both domestic and international filings. Similar patents may exist covering:

  • Analogous chemical structures.
  • Related therapeutic uses.
  • Formulatory innovations.

Foreign filings, especially in jurisdictions like the US, Europe, and China, influence patent validity and strategic positioning.

2. Related Patent Families

The applicant may have filed family members globally, indicating a broader patent strategy. These family patents can provide extended territorial coverage and support commercialization efforts.

3. Patent Thickets and Competitor Patents

The landscape may include overlapping patents or “patent thickets,” complicating freedom-to-operate analyses. Careful mapping of patent overlaps ensures that commercialization does not infringe existing rights.

4. Patent Litigation and Challenges

Potential patent disputes could arise if prior art threatens novelty. The strength of AU2022241491’s claims will depend on how well they distinguish over existing patents and publications.


5. Strategic Importance

The patent fills a potential gap in the current patent landscape, offering competitive advantages:

  • Strong exclusivity over specific compounds or uses.
  • Leverage in licensing negotiations.
  • Barrier to generic entry.

Its strength depends on the claim breadth and the robustness of the patent prosecution history.


Insights into Commercial and Legal Strategy

  • Claim Drafting: Focus on strategic claim breadth to maximize coverage while avoiding prior art.
  • Patent Family Networking: Synchronizing filings globally strengthens enforceability.
  • Monitoring and Defense: Vigilance against infringing patents and potential invalidation efforts.

Conclusion

The AU2022241491 patent exhibits carefully structured claims aimed at securing broad yet defensible rights over a novel pharmaceutical innovation. Its strategic positioning within Australia’s patent landscape suggests a well-planned approach to safeguard intellectual property and capitalize on therapeutic advancements.

The patent's strength hinges on its claim specificity, differentiation over prior art, and alignment with global patent strategies, positioning it as a significant asset for the applicant's commercial and research pursuits.


Key Takeaways

  • Broader claims enhance market exclusivity, but must overcome prior art hurdles.
  • Detailed claims on chemical structure and therapeutic use secure comprehensive protection.
  • Global patent family support amplifies market leverage and legal strength.
  • Monitoring patent landscapes is critical to uncover potential infringement risks.
  • Clear differentiation from existing patents ensures robust enforceability in Australia and internationally.

FAQs

Q1: How does AU2022241491 differ from existing patents in the same therapeutic area?
A1: It likely introduces a novel chemical entity or method of use not disclosed or claimed in prior art, with specific structural or functional features providing inventive differentiation.

Q2: Can the claims be challenged for lack of novelty or inventive step?
A2: Yes, prior art searches and patent examination data are necessary to assess these legal parameters. Strategic claim drafting aims to mitigate such risks.

Q3: What is the importance of dependent claims in this patent?
A3: Dependent claims refine and narrow the scope, providing fallback positions if broader claims face invalidation, thus strengthening overall patent defensibility.

Q4: How can this patent impact the development of biosimilars or generics?
A4: Broad or overlapping claims can act as barriers, delaying or preventing generic entry. The details determine how easily competitors can design around the patent.

Q5: What is the future potential for patent AU2022241491?
A5: Its value depends on continued patent prosecution, its enforceability, the strength over competitors’ patents, and the ongoing development pipeline.


References

[1] Australian Patent AU2022241491, Official Publication.
[2] Patent Classification Resources, IP Australia.
[3] Global Patent Landscape Reports, WIPO and EPO.

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