Study identifier:D8850C00005
ClinicalTrials.gov identifier:NCT04896541
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase I Double-blind, Placebo-controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AZD7442 in Healthy Japanese Participants
COVID-19
Phase 1
Yes
-
All
40
Interventional
18 Years - 55 Years
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: -
Primary Purpose: Prevention
Verified 01 Jun 2024 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: AZD7442 Single dose (IM injections or IV administration) of AZD7442 or saline placebo on Day 1. | Biological/Vaccine: AZD7442 300 mg IM(male) Single dose of 300 mg of AZD7442 or saline placebo on Day 1. Biological/Vaccine: AZD7442 600 mg IM (male) Single dose of 600 mg of AZD7442 or saline placebo on Day 1. Biological/Vaccine: AZD7442 300 mg IV (male and female) Single dose of 300 mg of AZD7442 or saline placebo on Day 1. Biological/Vaccine: AZD7442 1000 mg IV (male) Single dose 1000 mg of AZD7442 or saline placebo on Day 1. |
Experimental: placebo Single dose (× 2 separate IM injections or IV administration) of AZD7442 or saline placebo on Day 1. | Biological/Vaccine: AZD7442 300 mg IM(male) Single dose of 300 mg of AZD7442 or saline placebo on Day 1. Biological/Vaccine: AZD7442 600 mg IM (male) Single dose of 600 mg of AZD7442 or saline placebo on Day 1. Biological/Vaccine: AZD7442 300 mg IV (male and female) Single dose of 300 mg of AZD7442 or saline placebo on Day 1. Biological/Vaccine: AZD7442 1000 mg IV (male) Single dose 1000 mg of AZD7442 or saline placebo on Day 1. |