CI

At a glance

ClinicalIndex Comparison Record
Phase 3Active· 556 target
Drug / intervention
BCG (Bacillus Calmette-Guérin) vaccine +1 morebiological
Likely dose
BCG (Bacillus Calmette-Guérin) vaccine 0.1 mlfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05507671
NCT05507671Phase 3ActiveUpdate OverdueUpdated 10mo ago · Completion was 35mo ago
Enrollment Stalled

The Role of the Bacillus Calmette-Guérin Vaccine (BCG) in the Clinical Evolution of COVID-19 and in the Efficacy of Anti-SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus 2) Vaccines

Oswaldo Cruz Foundation·interventional·Posted Aug 19, 2022·Updated Aug 8, 2025

In Brief

A Phase 3 clinical trial evaluating BCG (Bacillus Calmette-Guérin) vaccine and Placebo for COVID-19. Active but no longer recruiting, targeting 556 participants across 4 sites.

Signals

Enrollment appears stalled

Detailed Summary

Clinical trial with randomized allocation in two arms (BCG vaccine versus placebo) of volunteers at risk but not yet infected nor vaccinated against SARS-CoV-2. Initially will be evaluated whether BCG has a protective role against severe form of the disease. After participants are vaccinated against COVID-19, it will be evaluated whether BCG favors the vaccine's efficacy. Volunteers will be recruited in three Brazilian states, with at least 250 seronegative in each group. The BCG-trained immunity stimulus will be investigated by assessing cytokines at D0 and D60 in a subsample of 50 participants per group. Until being vaccinated against COVID-19, the participants will be followed for up to 6 months, with visits scheduled every 2 months for interviews and immunoglobulin G (IgG) anti-SARS-CoV-2 antibodies. Those who become symptomatic at any time during the follow-up will be guided and monitored remotely daily until the end of their clinical evolution. After being vaccinated against COVID-19, visits to participants will be adjusted for the time of vaccination (VD), 20 days after the 1st dose (P1) and at least 30 days (P2) after the 2nd dose, with the aim of comparing the efficacy of the anti-SARS-CoV-2 vaccine in the two groups in the short and medium term. The study's conclusions on the efficacy of BCG in preventing severe COVID-19 will be based on: incidence of SARS-Cov-2 infection (defined as the emergence of IgG over the follow-up period); incidence of illness by COVID-19 (defined as the presence of symptoms among infected participants); intensity and duration of symptoms between cases of COVID-19 and frequency and duration of hospitalizations for COVID-19 in each group. The occurrence, type, frequency and intensity of adverse effects associated with vaccination of adults with BCG will be reported. The study's conclusions regarding the effect of BCG on efficacy of vaccines against COVID-19 will be based on: frequency of anti-SARS-CoV-2 neutralizing antibodies after the vaccine' 1st and 2nd doses in both groups.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCOVID-19
CountriesBrazil

Timeline

Phase 3ActiveOverdue
20222023202420252026
First PostedAug 19, 2022
Enrollment StartMay 27, 2021
Primary CompletionJul 31, 2023
Study CompletionDec 31, 2025
TodayJul 2, 2026
Enrollment to primary: 2.2 yearsPosted 3.9 years ago

Interventions

BCG (Bacillus Calmette-Guérin) vaccinebiological

Application of BCG vaccine (0.1 ml intradermal) in the right arm deltoid insertion

Placeboother

Application of BCG solvent (0.1 ml intradermal) in the right arm deltoid insertion