CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


BBV152BWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (4)


Name (Synonyms) Correlation
drug279 BBV152A Wiki 1.00
drug281 BBV152C Wiki 1.00
drug3018 survey Wiki 0.41
drug1822 Placebo Wiki 0.06

Correlated MeSH Terms (2)


Name (Synonyms) Correlation
D045169 Severe Acute Respiratory Syndrome NIH 0.05
D018352 Coronavirus Infections NIH 0.04

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 An Adaptive Phase 1, Followed by Phase 2 Randomized, Double-blind, Multicenter Study to Evaluate the Safety, Reactogenicity, Tolerability, and Immunogenicity of the BBV152 in Healthy Volunteers

The study is designed to evaluate the safety, reactogenicity, tolerability, and immunogenicity of three investigational vaccine groups and one placebo group in healthy volunteers who receive two intramuscular doses of BBV152 vaccine formulations. A total sample size of 1125 healthy volunteers, with 375 and 750 volunteers in phase 1 and 2 studies, respectively.

NCT04471519 Covid19 SARS-CoV Infection Biological: BBV152A Biological: BBV152B Biological: BBV152C Biological: Placebo
MeSH:Coronavirus Infections Severe Acute Respiratory Syndrome

Primary Outcomes

Description: Safety

Measure: Phase 1: Occurrence of adverse events and Serious Adverse events

Time: Through study completion, an average of 6 months

Description: Pre- and Post-vaccination immune response

Measure: Phase 2: Evaluation of Neutralizing Antibody Titers

Time: Through study completion, an average of 6 months

Secondary Outcomes

Description: Pre- and Post-vaccination immune response

Measure: Phase 1: Evaluation of Neutralizing Antibody Titers

Time: Through study completion, an average of 6 months

Description: Safety

Measure: Phase 2: Occurrence of adverse events and Serious Adverse events

Time: Through study completion, an average of 6 months


No related HPO nodes (Using clinical trials)