COVERAGE FRANCE
A French national adaptative platform trial to evaluate outpatient treatments against COVID-19
Topic
COVID-19
Sponsor
Bordeaux University Hospital
Coordinating investigator
Denis MALVY MD, PhD – Bordeaux University Hospital / Xavier ANGLARET MD – Bordeaux University Hospital
Short description
COVERAGE trial is a multicentric adaptative randomized controlled clinical trial platform evaluating several treatment strategies against COVID19 in outpatients with aggravating risk factors.
Study design
Multicenter, randomized, controlled clinical trial with for each drug :
- A safety study pilot phase
- An efficacy study phase. The data collected during the pilot phase, combined with new external data that emerged during the period, will be used to position treatments for the efficacy phase
Primary objective
- Pilot phase : Evaluate the tolerance of experimental treatments for drugs given for the first time (« first in home-based care ») in ambulatory individuals with COVID-19 with aggravating risk factors.
- Efficacy Phase : To estimate the effectiveness of experimental ambulatory treatments, compared to vitamin supplementation, in reducing the risk of hospitalization, oxygen therapy indication or death in ambulatory individuals with COVID-19 with aggravating risk factors.
Primary endpoint
- Pilot Phase : Proportion of participants who had a Grade 3 or 4 adverse event [ Time Frame: From inclusion (day0) to day 14 ]
- Efficacy phase : Death [ Time Frame: From inclusion (day0) to day 14 ]
Proportion of participants with an occurrence of death - Efficacy phase : oxygen therapy [ Time Frame: From inclusion (day0) to day 14 ]
Proportion of participants who had an indication for oxygen therapy - Efficacy phase : hospitalization [ Time Frame: From inclusion (day0) to day 14 ]
Proportion of participants who had an indication for hospitalization
Study population
Corona Virus Infection, Sars-CoV2
Intervention
Vitamins, Telmisartan, Ciclesonide, interferon β-1b
Number of subjects
412 participants
Participating country(ies) and sites
France, 7 sites
Study duration
436 days
Funding
French Ministry of Health and labeled France National Research Priority
UMS MART/EUCLID activities
Methodology, Statistical aspects, Data management, Global coordination of the trial