256
Participants
Start Date
August 23, 2020
Primary Completion Date
November 22, 2021
Study Completion Date
November 22, 2021
AZD1222
For subjects in part 1 will have that route of Administration as Intramuscular, 5 × 1010 vp (nominal, ± 1.5 × 1010 vp) on V2
0.9% (w/v) saline
For subjects in placebo will have that route of Administration as Intramuscular 0.9% (w/v) saline on V2 and V6.
Research Site, Fukuoka
Research Site, Hachioji-shi
Research Site, Minatoku
Research Site, Sumida-ku
Research Site, Toshima-ku
Lead Sponsor
Iqvia Pty Ltd
INDUSTRY
AstraZeneca
INDUSTRY