Bioequivalence Study of Vigabatrin ORPHELIA Pharma 500mg Soluble Tablets and SabrilTM 500mg Granules for Oral Administration

PHASE1CompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

April 4, 2017

Primary Completion Date

August 8, 2017

Study Completion Date

August 8, 2017

Conditions
Therapeutic Equivalency
Interventions
DRUG

VGB-ST

Single oral administration of 500 mg VGB-ST

Trial Locations (1)

38610

Eurofins Optimed, Gières

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Orphelia Pharma

INDUSTRY

NCT04468282 - Bioequivalence Study of Vigabatrin ORPHELIA Pharma 500mg Soluble Tablets and SabrilTM 500mg Granules for Oral Administration | Biotech Hunter | Biotech Hunter