Open-label, Non-randomized, Non-comparative, Phase II Study of Safety and Immunogenicity of Combination of AZD1222 and rAd26-S for COVID-19 Prevention

PHASE2CompletedINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

March 5, 2021

Primary Completion Date

October 30, 2021

Study Completion Date

March 18, 2022

Conditions
COVID-19
Interventions
BIOLOGICAL

AZD1222

"AZD1222 (0.5 ml per dose) contains:~Active substance: ChAdOx1 nCoV-19, a replicant-deficient simian adenoviral vector in the amount of 5 х 10\^10 particles per dose.~Solution for intramuscular injection, supplied in vials (5 mL, up to 10 doses per vial) in a carton box."

BIOLOGICAL

rAd26-S

"Component I (0.5 ml per dose) contains:~Active substance: recombinant adenovirus serotype 26 particles containing the SARS-CoV-2 protein S gene, in the amount of (1.0±0.5) х 10\^11 particles per dose.~Solution for intramuscular injection, supplied in vials (3 mL, 5 doses per vial) in a carton box"

Trial Locations (1)

Unknown

"Public legal entity Baku Health Center", Baku

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

AstraZeneca

INDUSTRY

collaborator

Russian Direct Investment Fund

INDUSTRY

collaborator

The Gamaleya National Center of Epidemiology & Microbiology

UNKNOWN

lead

R-Pharm

INDUSTRY