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Clinical Trial 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 participants with DSWPD.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04652882
Study type Interventional
Source Vanda Pharmaceuticals
Contact Vanda Pharmaceuticals Inc.
Phone 202-734-3400
Email VEC162@vandapharma.com
Status Recruiting
Phase Phase 3
Start date December 9, 2020
Completion date December 2025

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