Prucalopride in pediatric patients with fecal retention

$0M01FY2000RRNIH

Children'S Hosp Pittsburgh/Upmc Hlth Sys, Pittsburgh PA

Investigators

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Abstract

Objectives of this trial are to characterize the efficacy, safety and the tolerability and steady-state plasma levels after once-daily oral dosing of prucalopride as a solution given to pediatric subjects with functional fecal retention for an 8-week treatment period

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