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Cannabidiol Oral Solution for the Treatment of Patients With Prader-Willi Syndrome

Prader-Willi Syndrome Clinical Trial

Official title:
A Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study to Assess the Efficacy, Safety, and Tolerability of Cannabidiol Oral Solution for the Treatment of Patients With Prader-Willi Syndrome

Clinical Trial Summary

The primary objective of this study is to assess the efficacy of cannabidiol oral solution on hyperphagia-related behavior in patients with Prader-Willi Syndrome (PWS). The secondary objectives of this study are to assess the efficacy, safety and tolerability, impact on quality of life, and impact on physical activity of cannabidiol oral solution in patients with PWS.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02844933
Study type Interventional
Source Radius Pharmaceuticals, Inc.
Contact
Status Terminated
Phase Phase 2
Start date May 9, 2018
Completion date July 31, 2019
View Details
See also
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