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Clinical Trial Summary

This is a randomized, double blind, two arms, placebo controlled, clinical trial to study to evaluate the the safety and efficacy of Mycobacterium w in combination with standard of care versus placebo with standard of care for preventing the progression of COVID-19 disease and for reduction in transfer to ICU in COVID-19 infected patients admitted to the hospital.


Clinical Trial Description

Total 480 hospitalized adult eligible patients will be randomized in 1:1 ratio to receive either Mw+SOC or placebo+SOC for first 3 days post-randomization. Daily clinical evaluation of patient will be performed till discharge from hospital or till ICU admission. Study duration for each patient will be approximately up to 28 days, or discharge from hospital or transfer to ICU, whichever is earlier. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04358809
Study type Interventional
Source Cadila Pharnmaceuticals
Contact Anil Avhad, MBBS
Phone 919833454044
Email anil.avhad@cadilapharma.co.in
Status Recruiting
Phase Phase 3
Start date June 30, 2020
Completion date April 30, 2021

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