Overview

Evaluating the Effects of Tasimelteon vs. Placebo in Treating Pediatric Insomnia

Status:
RECRUITING
Trial end date:
2028-01-01
Target enrollment:
Participant gender:
Summary
This is a multicenter, double-blind, randomized study to evaluate the efficacy and safety of a daily single oral dose of tasimelteon and matching placebo in male and female pediatric participants with insomnia disorder.
Phase:
PHASE3
Details
Lead Sponsor:
Vanda Pharmaceuticals