drugset / Trial / NCT01142154

Pharmacokinetics and Safety Study of Single and Multiple Oral Doses Prodarsan™ in Patients With Cockayne Syndrome

NCT01142154 ↗

Phase 1/2 Completed 5 enrolled DNage B.V.
Non-randomizedSingle-groupOpen-label

Summary

This study is to compare the exposure of orally administered Prodarsan to the intravenous dosed Osmitrol (10% solution) in Cockayne Syndrome (CS) patients. Also the pharmacokinetics of single and multiple orally dosed Prodarsan will be evaluated and compared to intravenous dose of Osmitrol in CS patients.

Timeline

Start
2010-06
Primary completion
2010-09
Completion
2011-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Prodarsan Unknown — Oral

Indications