drugset / Trial / NCT01906866

Efficacy and Safety of Circadin® in the Treatment of Sleep Disturbances in Children With Neurodevelopment Disabilities

NCT01906866

Phase 3 Completed 125 enrolled Neurim Pharmaceuticals Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to establish the efficacy and safety of Circadin in children with neurodevelopmental disorders and to determine the dose, this randomized, placebo-controlled study is planned to evaluate the efficacy of a double-blind, 13 week treatment period with Circadin 2/5mg in improving maintenance of sleep, sleep latency and additional parameters in children with neurodevelopmental disabilities. The efficacy and safety of Circadin 2/5 mg will continue to be assessed during an open-label extension period of 13 weeks.

Timeline

Start
2013-10
Primary completion
2018-03-27
Completion
2018-03-27

Drugs

EvaluationDrugModalityDoseRoute
Comparator Melatonin Small molecule 2 mg
Comparator Melatonin Small molecule 5 mg
Comparator Melatonin Small molecule 10 mg

Indications