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Completed Phase 2 Interventional Results available

Tradipitant in Treatment-resistant Pruritus Associated With Atopic Dermatitis

ClinicalTrials.gov ID: NCT02651714

Public ClinicalTrials.gov record NCT02651714. 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, 4:04 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

A Multicenter, Randomized, Double-blind, Placebo-controlled Study to Assess the Safety and Efficacy of Tradipitant in Treatment-resistant Pruritus Associated With Atopic Dermatitis

Study identification

NCT ID
NCT02651714
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Vanda Pharmaceuticals
Industry
Enrollment
168 participants

Conditions and interventions

Interventions

  • Tradipitant Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 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
Jan 18, 2016
Primary completion
Aug 3, 2017
Completion
Aug 3, 2017
Last update posted
Jun 12, 2024

2016 – 2017

United States locations

U.S. sites
28
U.S. states
16
U.S. cities
25
Facility City State ZIP Site status
Vanda Investigational Site Encinitas California 92024
Vanda Investigational Site Encino California 91436
Vanda Investigational Site Lomita California 90717
Vanda Investigational Site San Diego California 92122
Vanda Investigational Site San Diego California 92123
Vanda Investigational Site Miami Florida 33126
Vanda Investigational Site Miami Florida 33136
Vanda Investigational Site Ormond Beach Florida 32174
Vanda Investigational Site Columbus Georgia 31904
Vanda Investigational Site Plainfield Indiana 46168
Vanda Investigational Site Crowley Louisiana 70526
Vanda Investigational Site St Louis Missouri 63110
Vanda Investigational Site Las Vegas Nevada 89119
Vanda Investigational Site New York New York 10022
Vanda Investigational Site New York New York 10075
Vanda Investigational Site High Point North Carolina 27262
Vanda Investigational Site Wilmington North Carolina 28405
Vanda Investigational Site Winston-Salem North Carolina 27104
Vanda Investigational Site Portland Oregon 97239
Vanda Investigational Site Philadelphia Pennsylvania 19104
Vanda Investigational Site Johnston Rhode Island 02919
Vanda Investigational Site Charleston South Carolina 29407
Vanda Investigational Site Houston Texas 77030
Vanda Investigational Site Pflugerville Texas 78660
Vanda Investigational Site San Antonio Texas 78218
Vanda Investigational Site West Jordan Utah 84088
Vanda Investigational Site Seattle Washington 98101
Vanda Investigational Site Spokane Washington 99202

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 NCT02651714, 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 Jun 12, 2024 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02651714 live on ClinicalTrials.gov.

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