Efficacy, safety, and lot-to-lot immunogenicity of an inactivated SARS-CoV-2 vaccine (BBV152): interim results of a randomised, double-blind, controlled, phase 3 trial
Clinical Trial
[키워드] 1:1
95% CI
absence
Administered
Adults
adverse event
age
Analysis
anaphylaxis
assigned
Bharat
chronic conditions
clinical
Clinical efficacy
clinical trial
clinically
clinics
computer-generated
Council
COVID-19
COVID-19 infection
Cutoff
deaths
dependent on
distribution
dose
double-blind
Efficacy
evaluate
Follow-up
groups
healthy
hospital
immunocompromising condition
immunological
immunosuppressive
inactivated
India
interim analysis
intramuscular dose
investigators
laboratory-confirmed
median
medical condition
multicentre
Nurse
occurred
Occurrence
outcome
outcomes
participant
Participants
per-protocol population
Phase 3
phase 3 trial
Placebo
placebo group
placebo recipients
placebo-controlled
Primary outcome
proportion
raised
randomisation
randomised
Randomly
reactogenicity
receive
recipient
recruited
Registered
registry
reported
Research
safety population
SARS-CoV-2 vaccine
second dose
Serious Adverse Event
seronegative participant
severity
significant difference
Sponsor
stratified
study population
symptomatic
symptomatic COVID-19 disease
the vaccine
therapy
Toll-like receptor
Treatment
treatment group
Trial
Vaccine
virion
[DOI] 10.1016/S0140-6736(21)02000-6 PMC 바로가기 [Article Type] Clinical Trial
[DOI] 10.1016/S0140-6736(21)02000-6 PMC 바로가기 [Article Type] Clinical Trial