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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Evaluating the Effects of Tasimelteon vs. Placebo on Jet Lag Type Insomnia

ClinicalTrials.gov ID: NCT03373201

Public ClinicalTrials.gov record NCT03373201. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 7:04 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The aim of this study is to investigate tasimelteon vs. placebo on sleep in healthy individuals after a phase advance in jet lag type insomnia.

Study identification

NCT ID
NCT03373201
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Vanda Pharmaceuticals
Industry
Enrollment
320 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 16, 2017 (Actual)
Primary completion
Mar 5, 2018 (Actual)
Completion
Mar 5, 2018 (Actual)
Last update posted
Sep 15, 2023

2017 – 2018

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Vanda Investigational Site Little Rock Arkansas 72211 —
Vanda Investigational Site Alameda California 94501 —
Vanda Investigational Site San Diego California 92103 —
Vanda Investigational Site Santa Monica California 90404 —
Vanda Investigational Site Oakland Park Florida 33334 —
Vanda Investigational Site Atlanta Georgia 30342 —
Vanda Investigational Site Chevy Chase Maryland 20815 —
Vanda Investigational Site St Louis Missouri 63141 —
Vanda Investigational Site New York New York 10019 —
Vanda Investigational Site Cincinnati Ohio 45212 —
Vanda Investigational Site Oklahoma City Oklahoma 73112 —
Vanda Investigational Site Houston Texas 77063 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03373201, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 15, 2023 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03373201 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →