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Trial to Evaluate Efficacy and Safety of Apraglutide in SBS-IF — STARS  

Short Bowel Syndrome Clinical Trial

Official title:
A Multicenter, Double-blind, Randomized, Placebo-controlled Trial to Evaluate the Efficacy and Safety of Apraglutide in Adult Subjects With Short Bowel Syndrome and Intestinal Failure (SBS-IF)

Clinical Trial Summary

The primary objective of the trial is the confirmation of the efficacy of apraglutide to evaluate the efficacy of weekly subcutaneous apraglutide in reducing parenteral support dependency.

Clinical Trial Description

This is an international, multicenter, double-blind, randomized, placebo-controlled, trial to evaluate the efficacy and safety of weekly SC injections of apraglutide in adult subjects with SBS-IF. The active pharmaceutical ingredient is apraglutide, a GLP-2 analogue. The trial consists of a screening phase, a treatment phase of 48 weeks, and a safety follow-up phase. Trial participants will receive, after successful screening, once weekly apraglutide. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04627025
Study type Interventional
Source VectivBio AG
Contact
Status Completed
Phase Phase 3
Start date January 26, 2021
Completion date February 22, 2024
View Details
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