NCT07446439PHASE3RecruitingAccepts Healthy Volunteers
A Study to Evaluate Tradipitant on Treating Nausea and Vomiting Induced by GLP-1R Agonist Use
Vanda Pharmaceuticals
Start Date
3/27/2026
Completion Date
12/1/2026
Summary
The goal of this study is to measure the effects of using Tradipitant to treat nausea and vomiting induced by GLP-1R agonist use in adults with class I or class II obesity, or adults who are overweight with at least one weight-related condition. The study is placebo-controlled with two treatment arms.
Eligibility Criteria
Age Range: 18 years to 65 years
Inclusion Criteria:
* Body Mass Index ≥ 25 and \< 40 kg/m\^2
* No serious medical problems or chronic diseases, specifically no type I or type II diabetes
Exclusion Criteria:
* Another disorder that contributes to gastrointestinal symptoms
* History of intolerance and/or hypersensitivity to NK-1 receptor antagonists
* History of intolerance and/or hypersensitivity to GLP-1 receptor agonists
* Exposure to any investigational medication within the past 60 days
Interventions
DRUG
Tradipitant
DRUG
Placebo
Conditions
Nausea and VomitingObesity
Locations
Vanda Investigational Site
Los Angeles, California 90025
United States
Vanda Investigational Site
San Diego, California 92108
United States
Vanda Investigational Site
San Jose, California 95124
United States
Vanda Investigational Site
Tampa, Florida 33613
United States
Vanda Investigational Site
Hamilton, New Jersey 08690
United States
Vanda Investigational Site
New York, New York 10016
United States
Vanda Investigational Site
Syosset, New York 11791
United States
Vanda Investigational Site
Plano, Texas 75024
United States
Vanda Investigational Site
San Antonio, Texas 78215
United States
Vanda Investigational Site
Burke, Virginia 22015
United States