Tradipitant for Nausea and Vomiting from Weight Loss Drugs

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

Recruiting Phase 3 Interventional Study
Nausea and Vomiting Obesity
Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 65
Sex
Any
Trial phase
Phase 3
Study type
Interventional
Purpose
Treatment
Participants needed
280 (estimated)
Sponsor
Vanda Pharmaceuticals · Industry
Who this trial is looking for

This trial is looking for adults with obesity or who are overweight and experiencing nausea and vomiting from specific weight loss medications. Participants will receive either the study drug, Tradipitant, or a placebo to see how it helps with their symptoms.

Are You a Good Fit for This Trial?

You may be able to join if

  • I have a Body Mass Index between 25 and 40
  • I do not have serious medical problems
  • I do not have type I or type II diabetes

You may not be able to join if

  • I have another condition causing stomach symptoms
  • I have been intolerant or allergic to NK-1 receptor antagonists
  • I have been intolerant or allergic to GLP-1 receptor agonists
  • I have taken any experimental medication in the past 60 days

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

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About This Trial

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.

Trial Locations
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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 …
Contacts

Vanda Pharmaceuticals

(202) 734-3400

clinicaltrials@vandapharma.com

CONTACT