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Efficacy And Safety Evaluation of Glepaglutide in Treatment of Short Bowel Syndrome (SBS) — EASE SBS 1  

Short Bowel Syndrome Clinical Trial

Official title:
A Phase 3, International, Multicenter, Randomized, Double-blind, Placebo-controlled Trial to Evaluate the Efficacy and Safety of Glepaglutide in Patients With Short Bowel Syndrome (SBS)

Clinical Trial Summary

The primary objective of the trial is to confirm the efficacy of glepaglutide in reducing parenteral support volume in patients with short bowel syndrome. Glepaglutide is the International Nonproprietary Name and USAN for ZP1848.

Clinical Trial Description

A Phase 3, international, multicenter, randomized, double-blind, placebo-controlled trial to evaluate the efficacy and safety of glepaglutide subcutaneous (SC) injections in patients with short bowel syndrome (SBS). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03690206
Study type Interventional
Source Zealand Pharma
Contact
Status Completed
Phase Phase 3
Start date October 4, 2018
Completion date July 26, 2022
View Details
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