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Different Doses of Naronapride vs. Placebo in Gastroparesis — MOVE-IT  

Gastroparesis Clinical Trial

Official title:
Double-blind, Randomised, Placebo-controlled, Dose-finding Phase IIb Trial to Evaluate the Efficacy, Safety, and Tolerability of a 12-week-treatment With Naronapride in Adult Participants With at Least Moderate Idiopathic or Diabetic Gastroparesis

Clinical Trial Summary

This is a double-blind, randomized, multicenter, placebo-controlled, comparative phase II dose-finding trial. The trial will be conducted with four treatment groups in the form of a parallel group comparison and will serve to compare oral treatment with daily doses of 10, 20, or 40 mg Naronapride vs. placebo for the treatment of patients with Gastroparesis.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05621811
Study type Interventional
Source Dr. Falk Pharma GmbH
Contact
Status Recruiting
Phase Phase 2
Start date January 3, 2023
Completion date April 2025
View Details
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