drugset / Trial / NCT03285308

A Safety and Efficacy Study of Relamorelin in Diabetic Gastroparesis 01

NCT03285308 ↗

Phase 3 Terminated 336 enrolled Allergan
RandomizedParallel-groupDouble-blindTreatment

Summary

This study will evaluate the safety and efficacy of relamorelin compared to placebo in participants with diabetic gastroparesis. Participants will report daily severity scores of their diabetic gastroparesis symptoms.

Timeline

Start
2017-09-29
Primary completion
2020-07-08
Completion
2020-07-08

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