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

RecruitingPhase 3Healthy volunteers welcome

The Thetis Study: A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy of Tradipitant on Nausea and Vomiting After GLP-1R Agonist Administration in Healthy Overweight or Obese Volunteers

Who can join

Ages 18 to 65 · All sexes · Healthy volunteers welcome

Full eligibility criteria
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

About the study

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.

What is being tested

Sponsor: Vanda Pharmaceuticals · Participants: 280 · Started: Mar 27, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07446439

Locations in the U.S.

CaliforniaVanda Investigational Site, Los Angeles
Vanda Investigational Site, San Diego
Vanda Investigational Site, San Jose (Not yet recruiting)
FloridaVanda Investigational Site, Tampa
New JerseyVanda Investigational Site, Hamilton (Not yet recruiting)
New YorkVanda Investigational Site, New York (Not yet recruiting)
Vanda Investigational Site, Syosset (Not yet recruiting)
TexasVanda Investigational Site, Plano (Not yet recruiting)
Vanda Investigational Site, San Antonio (Not yet recruiting)
VirginiaVanda Investigational Site, Burke (Not yet recruiting)

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.