A Trial in Healthy Volunteers, to Evaluate the Tolerability and Cardiac Safety of Prucalopride

PHASE1CompletedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

January 31, 2000

Primary Completion Date

March 31, 2000

Study Completion Date

March 31, 2000

Conditions
Constipation
Interventions
DRUG

prucalopride

The dose will be consecutively escalated in 2 mg steps per day, starting from 2 mg up to 20 mg once daily or until severe drug-related adverse events occur (= individual maximum tolerable dose, on decision of the subject and/or investigator).

OTHER

Placebo

During the placebo session, the number of placebo tablets will be consecutively escalated in an identical way as described for prucalopride. This means 1 tablet more every day, up to 10 tablets.

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Movetis

INDUSTRY