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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

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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