drugset / Trial / NCT02690025

A Phase 2 Trial Testing ZP1848 in Patients With SBS

NCT02690025 ↗

Phase 2 Completed 18 enrolled Zealand Pharma Larix A/S · collab
RandomizedCrossoverQuadruple-blindTreatment

Summary

A proof-of-concept, dose finding, controlled, single-center, randomized, double-blind, fixed dose phase 2 trial with ZP1848 in patients with Short Bowel Syndrome.

Timeline

Start
2016-02
Primary completion
2017-05
Completion
2017-05

Outcome

Met primary endpoint

paper adjusted mean faecal output by -592 g/day (95% CI -913 to -272; p=0·002) PMID 30880176 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Glepaglutide Peptide 0.1 mg Subcutaneous
Subject Glepaglutide Peptide 1 mg Subcutaneous
Subject Glepaglutide Peptide 10 mg Subcutaneous

Indications