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Completed Phase 3 Interventional

Evaluating the Safety and Efficacy of Tradipitant vs. Placebo in Idiopathic and Diabetic Gastroparesis

ClinicalTrials.gov ID: NCT04028492

Public ClinicalTrials.gov record NCT04028492. 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 Jul 22, 2026, 2:09 PM EDT

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

Official title

VP-VLY-686-3301: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase Iii Study To Assess The Efficacy Of Tradipitant In Relieving Symptoms Of Gastroparesis

Study identification

NCT ID
NCT04028492
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Vanda Pharmaceuticals
Industry
Enrollment
992 participants

Conditions and interventions

Interventions

  • Tradipitant Drug
  • Placebo Drug
  • Open Label Tradipitant Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Aug 19, 2019
Primary completion
Feb 20, 2025
Completion
Feb 20, 2025
Last update posted
Jul 23, 2025

2019 – 2025

United States locations

U.S. sites
36
U.S. states
23
U.S. cities
33
Facility City State ZIP Site status
Vanda Investigational Site Birmingham Alabama 53244
Vanda Investigational Site Peoria Arizona 85381
Vanda Investigational Site Little Rock Arkansas 72211
Vanda Investigational Site Chula Vista California 91910
Vanda Investigational Site La Jolla California 92093
Vanda Investigational Site Los Angeles California 90010
Vanda Investigational Site Los Angeles California 90026
Vanda Investigational Site Maitland Florida 32751
Vanda Investigational Site Palmetto Bay Florida 33157
Vanda Investigational Site Tampa Florida 33613
Vanda Investigational Site Morrow Georgia 30260
Vanda Investigational Site Wauconda Illinois 60084
Vanda Investigational Site West Des Moines Iowa 50265
Vanda Investigational Site Wichita Kansas 67214
Vanda Investigational Site Louisville Kentucky 40202
Vanda Investigational Site Marrero Louisiana 70072
Vanda Investigational Site Chevy Chase Maryland 20815
Vanda Investigational Site Boston Massachusetts 02114
Vanda Investigational Site Boston Massachusetts 02115
Vanda Investigational Site Chesterfield Missouri 63005
Vanda Investigational Site Las Vegas Nevada 89121
Vanda Investigational Site Brooklyn New York 11201
Vanda Investigational Site Charlotte North Carolina 28209
Vanda Investigational Site Raleigh North Carolina 27612
Vanda Investigational Site Columbus Ohio 43214
Vanda Investigational Site Huber Heights Ohio 45424
Vanda Investigational Site Edmond Oklahoma 73034
Vanda Investigational Site Tulsa Oklahoma 74104
Vanda Investigational Site Philadelphia Pennsylvania 19104
Vanda Investigational Site Chattanooga Tennessee 37421
Vanda Investigational Site Nashville Tennessee 37211
Vanda Investigational Site Houston Texas 77043
Vanda Investigational Site Houston Texas 77084
Vanda Investigational Site Plano Texas 75024
Vanda Investigational Site San Antonio Texas 78215
Vanda Investigational Site Salt Lake City Utah 84132

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 NCT04028492, 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 Jul 23, 2025 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04028492 live on ClinicalTrials.gov.

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