drugset / Trial / NCT01674166

Single Dose Pharmacokinetics of Prucalopride in Paediatric Subjects, With Functional Faecal Retention

NCT01674166

Phase 1 Completed 38 enrolled Movetis
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is characterize the pharmacokinetics of a single oral dose of 0.03 mg/kg prucalopride in paediatric subjects aged \>= 4 to \<= 12 years with functional faecal retention. Hypothesis: Pharmacokinetic profile of prucalopride in paediatric subjects is expected to resemble the adult pharmacokinetic profile

Timeline

Start
1998-11
Primary completion
1999-05
Completion
1999-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Prucalopride Small molecule 0.03 mg/kg Oral

Indications