Study identifier:D9190C00002
ClinicalTrials.gov identifier:NCT07824622
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase I, Randomized, Double-blind, Placebo-controlled Study to Assess the Safety and Pharmacokinetics of AZD0543 in Healthy Adults
Human Metapneumovirus Infection
Phase 1
Yes
-
All
144
Interventional
18 Years - 55 Years
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: -
Primary Purpose: Prevention
Verified 01 Nov 2026 by AstraZeneca
AstraZeneca
-
No locations available
| Arms | Assigned Interventions |
|---|---|
| Experimental: Cohort 1: Low Dose AZD0543 Participants will receive a single AZD0543 dose. | Biological/Vaccine: AZD0543 Sterile solution for injection or infusion administered as a single IM or IV dose on Day 1. |
| Placebo Comparator: Cohort 1: Placebo Participants will receive a single dose of placebo. | Other: Placebo Volume-matched 0.9% (w/v) sterile saline solution for injection or infusion administered as a single IM or IV dose on Day 1. |
| Experimental: Cohort 2: Medium Dose AZD0543 Participants will receive a single AZD0543 dose. | Biological/Vaccine: AZD0543 Sterile solution for injection or infusion administered as a single IM or IV dose on Day 1. |
| Placebo Comparator: Cohort 2: Placebo Participants will receive a single dose of placebo. | Other: Placebo Volume-matched 0.9% (w/v) sterile saline solution for injection or infusion administered as a single IM or IV dose on Day 1. |
| Experimental: Cohort 3: High Dose AZD0543 Participants will receive a single AZD0543 dose. | Biological/Vaccine: AZD0543 Sterile solution for injection or infusion administered as a single IM or IV dose on Day 1. |
| Placebo Comparator: Cohort 3: Placebo Participants will receive a single dose of placebo. | Other: Placebo Volume-matched 0.9% (w/v) sterile saline solution for injection or infusion administered as a single IM or IV dose on Day 1. |