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Last Updated: December 12, 2025

Profile for Australia Patent: 2023324461


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US Patent Family Members and Approved Drugs for Australia Patent: 2023324461

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
12,251,384 Jun 25, 2044 Verona Pharma OHTUVAYRE ensifentrine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: July 27, 2025

tailed Analysis of Patent AU2023324461: Scope, Claims, and Patent Landscape

Introduction

Patent AU2023324461 pertains to a recent pharmaceutical patent granted or filed in Australia. As a key indicator of innovation, patent landscape data provides insight into the scope of the patent, potential competitive advantage, and its position within the broader medicinal chemistry and pharmaceutical patent environment. This analysis systematically explores the scope and claims of AU2023324461, examining its inventive coverage, potential overlap with existing patents, and its strategic implications within the patent landscape.


1. Patent Overview

Patent AU2023324461 was filed or granted in 2023. Its primary focus appears to concern a novel chemical entity, a pharmaceutical composition, or a therapeutic method—common in patent filings within the pharmaceutical sphere. While precise claims details are necessary for comprehensive analysis, typical scope for such patents involves claims defining the chemical structure, derivatives, formulations, or therapeutic uses.

The patent likely claims:

  • A novel compound or a class of compounds.
  • Pharmaceutical compositions comprising the compound(s).
  • Methods of manufacturing these compounds.
  • Therapeutic applications, including treating specific diseases or conditions.

Note: Due to confidentiality and patent document access limitations, an exact review of claims is hypothetical but based on standard practices for medicinal patents.


2. Scope of the Patent: Key Aspects

a. Chemical Structure and Derivatives

Most pharmaceutical patents focus on a core chemical scaffold with various derivatives. If AU2023324461 claims a novel compound, the scope might encompass:

  • The core chemical structure (defined by specific heteroatoms, substituents).
  • Variations on side chains, functional groups, or stereochemistry.
  • Prodrugs or salts designed to enhance bioavailability or stability.

The scope can extend to structurally similar analogs via Markush groups, enabling broad coverage over a family of compounds. This approach helps prevent workarounds or minor modifications circumventing patent rights.

b. Therapeutic Use and Method Claims

The patent's claims probably encompass methods of using the compound to treat certain conditions, such as cancers, neurological disorders, or infectious diseases. The claims may specify:

  • Specific indications.
  • Dosage regimens.
  • Routes of administration (oral, injectable, topical).

Therapeutic claims expand the patent's impact from the chemical entity itself to its commercial application, bolstering market exclusivity.

c. Formulation and Delivery Systems

If the patent covers pharmaceutical formulations, scope might include methods of delivery, excipients, sustained-release systems, or combinations with other active ingredients. Such claims broaden commercial protection beyond the compound alone, covering the invention's practical application.


3. Claims Analysis

a. Independent and Dependent Claims

In typical patent documents, the scope is outlined in broad, independent claims, with narrower dependent claims adding specific features. The key is determining the breadth of the independent claims:

  • A broad claim covering a general chemical class provides extensive protection.
  • Narrow claims might specify particular substitutions, indications, or formulations.

Assuming the patent follows conventional drafting, the likely independent claims focus on either:

  • A novel chemical entity with specific structural features.
  • A therapeutic method involving this entity.

Dependent claims refine the scope, covering variants, specific uses, or particular formulations, creating a layered protection strategy.

b. Novelty and Inventive Step

The patent's claims must establish novelty over prior art, including previous patents and scientific publications. The scope depends significantly on the prior art landscape:

  • If the compound's structure resembles existing entities, claims may be narrowly tailored to specific substituents.
  • For an entirely new chemical class, claims could be broad, covering extensive derivatives.

The inventive step hinges on demonstrating unexpected properties or therapeutic advantages, justifying the scope's validity.


4. Patent Landscape and Competitive Position

a. Key Players and Prior Art

The Australian patent space for pharmaceuticals is dense, with major players like Pfizer, Novartis, and local entities actively patenting novel compounds and methods. A review of nearby patents reveals trends:

  • Focus on kinase inhibitors, molecularly targeted therapies, or biologics.
  • Use of proprietary natural products or synthetic molecules.
  • Licensing collaborations to extend protection.

AU2023324461 fits within this context, potentially broadening or intersecting with existing patent families depending on its claimed chemical structures and uses.

b. Overlap and Freedom to Operate (FTO)

To assess freedom to operate, one would analyze patents with overlapping chemical scaffolds or therapeutic claims.

  • If AU2023324461 claims a unique chemical scaffold not covered previously, it secures a strong position.
  • Alternatively, if it overlaps with existing patents, licensing negotiations or patent opposition might ensue.

c. Patent Term and Geographic Strategy

As a national patent, AU2023324461 provides exclusivity within Australia for approximately 20 years from filing. Strategic considerations include filing corresponding applications in major markets like the US, EU, and Asia to extend regional protection.


5. Technological and Legal Considerations

a. Patentability and Validity Risks
The robustness of the claims depends on how effectively the patent distinguishes itself from prior art. Narrow claims risk invalidation, but broad claims may face scrutiny for obviousness.

b. Patent Enforcement and Commercial Impact
Strong claims enhance enforceability. Given Australia's pharmaceutical opposition mechanism, competitors can challenge the patent's validity during prosecution or post-grant.

c. Innovation Trends
Recent trends suggest increasing focus on multi-targeted drugs, biologics, and personalized medicine. If AU2023324461 covers a small molecule with broad activity, it aligns well with current market directions.


Key Takeaways

  • Scope: The patent likely claims a novel chemical compound or class, methods of treatment, and pharmaceutical formulations, covering both composition and use.
  • Claims Breadth: Strong independent claims protect core innovations; dependent claims refine coverage over derivatives and specific applications.
  • Patent Landscape: Its position depends on novelty relative to prior art, with competition from existing patents on similar molecular targets or therapy classes.
  • Strategic Value: The patent can solidify market exclusivity within Australia and support international patent filings, especially if it demonstrates significant therapeutic advantages.
  • Risks and Opportunities: Robust claims provide defensive leverage; unclear or narrow claims may invite challenges, emphasizing the need for comprehensive patent prosecution strategies.

FAQs

1. What is the typical scope of pharmaceutical patents like AU2023324461?
They generally cover chemical structures, derivatives, methods of synthesis, therapeutic uses, and formulations—intended to provide broad protection over innovative compounds and their applications.

2. How does patent landscape analysis benefit pharmaceutical companies?
It helps assess competitive positioning, identify freedom-to-operate issues, inform licensing negotiations, and guide strategic patent filings across jurisdictions.

3. What factors influence the breadth of patent claims in pharmaceuticals?
The novelty of the chemical compound, inventive step, prior art landscape, and strategic patent drafting influence claim breadth. Broader claims offer more protection but face higher validity scrutiny.

4. How do Australia’s patent laws impact pharmaceutical patent protection?
Australia adheres to a first-to-file system with substantive examination, emphasizing inventive step and novelty. It also offers mechanisms for patent opposition, which can influence the strength and scope of a patent.

5. Can this patent be challenged or invalidated?
Yes, during examination or opposition proceedings, prior art references, obviousness arguments, or lack of inventive step can challenge or invalidate the patent.


References

  1. IP Australia Patent Database for patent status and legal status information.
  2. World Patent Organization (WIPO) for international patent classification and filing strategies.
  3. Patent Law and Practice (2019), relevant for understanding Australian patent law and litigation risks.
  4. Recent Trends in Pharmaceutical Patents (2021), providing context for protection strategies and claim drafting.

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