COVERAGE FRANCE

11 mai 2023

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