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Recruiting Phase 3 NCT07446439

A Study to Evaluate Tradipitant on Treating Nausea and Vomiting Induced by GLP-1R Agonist Use

Phase 3 – large-scale trial before approval
Conditions: Nausea and Vomiting Obesity

Sponsor: Vanda Pharmaceuticals

trial.available_in: БГ
Overview
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.
Who can participate
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
Tradipitant
DRUG
Placebo
DRUG
Locations 10
United States (10)
Vanda Investigational Site
Burke , Virginia
NOT_YET_RECRUITING
Vanda Pharmaceuticals
Vanda Investigational Site
Hamilton , New Jersey
NOT_YET_RECRUITING
Vanda Pharmaceuticals
Vanda Investigational Site
Los Angeles , California
Vanda Pharmaceuticals
Vanda Investigational Site
New York , New York
NOT_YET_RECRUITING
Vanda Pharmaceuticals
Vanda Investigational Site
Plano , Texas
NOT_YET_RECRUITING
Vanda Pharmaceuticals
Vanda Investigational Site
San Antonio , Texas
NOT_YET_RECRUITING
Vanda Pharmaceuticals
Vanda Investigational Site
San Diego , California
Vanda Pharmaceuticals
Vanda Investigational Site
San Jose , California
NOT_YET_RECRUITING
Vanda Pharmaceuticals
Vanda Investigational Site
Syosset , New York
NOT_YET_RECRUITING
Vanda Pharmaceuticals
Vanda Investigational Site
Tampa , Florida
Vanda Pharmaceuticals
Technical details
Status
Recruiting
Phase
Phase 3
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
65 Years
Healthy volunteers
No
Start date
27.03.2026
Completion date
01.12.2026
Registry ID
NCT07446439
Source
clinicaltrials.gov
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