drugset / Trial / NCT03383146

A Safety and Efficacy Study of Relamorelin in Diabetic Gastroparesis Study 04

NCT03383146 ↗

Phase 3 Terminated 450 enrolled Allergan
RandomizedParallel-groupTriple-blindTreatment

Summary

A 52-week study to compare the efficacy of relamorelin with that of placebo in participants with diabetic gastroparesis (DG) with respect to the core signs and symptoms of diabetic gastroparesis.

Timeline

Start
2018-02-01
Primary completion
2020-11-05
Completion
2020-11-05

Outcome

Outcome not reported

Stopped (Business): “The Relamorelin program is being terminated solely based on a business decision.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Relamorelin Peptide 10 ug Subcutaneous