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IVX-121

Phase 1

Healthy | Monoclonal antibody | Other |AstraZeneca PLC|Last Updated: Mar 4, 2024

Success Probability

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Market & Valuation

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Trial Design

UNCONTROLLED
Total Trials1
Total Enrollment140

FDA Designations

No designations recorded

Clinical trial landscape

IVX-121 · 1 trial · 1 indication

Phase 1 1
NCT05664334Safety and Immunogenicity of IVX-A12 in Healthy Older AdultsHealthy
COMPLETED140 Analytics
PHASE1COMPLETED
Safety and Immunogenicity of IVX-A12 in Healthy Older Adults
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Study Design & Arms

Interventions

NameTypeDescription
IVX-121BIOLOGICAL75 mcg of IVX-121 without MF59®
IVX-241BIOLOGICAL75 mcg of IVX-241 without MF59®
PlaceboBIOLOGICALDiluent
MF59®OTHERMF59® as an adjuvant
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Frequently asked questions about IVX-121

What is IVX-121?

IVX-121 is an investigational monoclonal antibody being developed by AstraZeneca PLC (ticker: AZN). It is currently in Phase 1 clinical development. The drug is being studied for use in healthy individuals, as part of a broader research program.

What is IVX-121 used for?

IVX-121 is being studied for use in healthy individuals. It is an investigational monoclonal antibody in Phase 1 clinical development. The drug is being evaluated for safety and immunogenicity, as part of a research program by AstraZeneca PLC.

Who makes IVX-121?

IVX-121 is being developed by AstraZeneca PLC, a biopharmaceutical company listed on the stock exchange under the ticker AZN. The drug is an investigational monoclonal antibody currently in Phase 1 clinical development.

What phase is IVX-121 in?

IVX-121 is in Phase 1 clinical development. It is an investigational monoclonal antibody being developed by AstraZeneca PLC. The drug is not yet approved and is still undergoing clinical trials to evaluate its safety and immunogenicity in healthy individuals.

What clinical trials is IVX-121 in?

IVX-121 is associated with clinical trial NCT05664334, titled "Safety and Immunogenicity of IVX-A12 in Healthy Older Adults." This Phase 1 trial has been completed and enrolled 140 participants. The trial was uncontrolled and not randomized or double-blinded.