14
Participants
Start Date
June 7, 2022
Primary Completion Date
June 4, 2024
Study Completion Date
June 4, 2024
REM0046127 High Dose
"Each subject will start with a 14-day placebo run-in period, followed by a 28-day treatment period and 7-day follow-up period.~REM0046127 high dose: 1400mg (700mg bid) oral suspension per day for 28 days"
REM0046127 Low Dose
"Each subject will start with a 14-day placebo run-in period, followed by a 28-day treatment period and 7-day follow-up period.~REM0046127 low dose: 350mg (175mg bid) oral suspension per day for 28 days"
Placebo
"Each subject will start with a 14-day placebo run-in period, followed by a 28-day treatment period and 7-day follow-up period.~Placebo: placebo oral suspension bid for 28 days and during the 14-days run-in phase"
BRC Amsterdam, Amsterdam
FISEVI Hospital Universitario Virgen del Rocio, Seville
Fundacion ACE, Barcelona
Lead Sponsor
reMYND
INDUSTRY