drugset / Trial / NCT05470270

Acceptability of a New Paediatric Formulation of Hydroxycarbamide in Children With Sickle Cell Disease.

NCT05470270

Phase 2 Completed 33 enrolled Theravia
NaSingle-groupOpen-labelTreatment

Summary

This is a prospective, interventional, phase II, open-label, multicentre, national, non-comparative study of a single administration of the new dispersible form of hydroxycarbamide at the usual dose in children with sickle cell disease who are already treated with the current form of hydroxycarbamide (Siklos® 100 mg and/or 1000 mg film-coated tablets).

Timeline

Start
2022-07-08
Primary completion
2022-10-28
Completion
2022-10-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Hydroxyurea Other / unclassified

Indications