TQT2 Study to Evaluate the Effect of MD1003 on Cardiac Repolarization in Healthy Adult Subjects

PHASE1UnknownINTERVENTIONAL
Enrollment

64

Participants

Timeline

Start Date

November 11, 2019

Primary Completion Date

March 5, 2020

Study Completion Date

March 5, 2020

Conditions
Healthy Volunteers
Interventions
DRUG

MD1003

Group A: Daily dose of 1200 mg of MD1003 from Day 1 to Day 8

DRUG

Moxifloxacin 400mg

Group B1: Moxifloxacin 400 mg on Day 1 Group B2: Moxifloxacin 400 mg on Day 9

DRUG

Placebo for MD1003

Group A: Placebo for MD1003 on Day -1 Group B1: Placebo for MD1003 on Day -1 Group B2: Placebo for MD1003 on Day -1

DRUG

Placebo for moxifloxacin

Group A: Placebo for moxifloxacin on Day 1 and Day 9 Group B1: Placebo for moxifloxacin on Day 9 Group B2: Placebo for moxifloxacin on Day 1

Trial Locations (1)

HA13UJ

RECRUITING

Parexel Early Phase Clinical Unit London, London

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

collaborator

ERT: Clinical Trial Technology Solutions

OTHER

lead

MedDay Pharmaceuticals SA

INDUSTRY