Finding studies
Finding studies
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Lead
Centre Hospitalier Universitaire de Saint Etienne
With
The study COVIDAXIS 1(Hydroxychloroquine (HCQ) versus placebo) will be realized on 600 participants and will be implemented first in as many centers as possible. Upon randomization, with 1:1 allocation ratio, healthcare workers involved in the management of suspected or confirmed COVID-19 cases will be assigned to one of the following 2 treatment groups: * Group 1.1: HCQ 200 mg : 2 tablets on the evening at Day 1 and 2 tablets on the morning at Day 2 and 1 tablet once daily afterwards * Group 1.2: Placebo of HCQ, 2 tablets on the evening at Day 1 and 2 tablets on the morning at Day 2 and 1 tablet once daily afterwards. The COVIDAXIS 2 (Lopinavir/ritonavir (LPV/r) versus placebo will be realized on 600 participants and will be implemented in already participating and newer centers in a second step (when LPV/r becomes available). Upon randomization, with 1:1 allocation ratio, healthcare workers involved in the management of suspected or confirmed COVID-19 cases will be assigned to one of the following 2 treatment groups: * Group 2.1: LPV/r 200/50 mg : 2 tablets twice daily * Group 2.2: Placebo of LPV/r, 2 tablets twice daily Participants will receive the randomized treatment for 2 months and will be followed upon a 2.5 months period. NB: there is no randomization procedure for participant inclusion in either COVIDAXIS 1 or COVIDAXIS 2
Age
18–any
Sex
ALL
Healthy volunteers
Accepted
