drugset / Trial / NCT02508649

Selepressin Evaluation Programme for Sepsis-Induced Shock - Adaptive Clinical Trial

NCT02508649 ↗

Phase 2/3 Terminated 868 enrolled Ferring Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a double-blind, randomised, placebo-controlled, two-part adaptive clinical trial. The trial is designed to investigate the efficacy and safety of multiple dosing regimens of selepressin and to confirm the efficacy and safety of one dosing regimen in treatment of adult patients with septic shock requiring vasopressor.

Timeline

Start
2015-07
Primary completion
2017-10-03
Completion
2018-02-26

Outcome

Missed primary endpoint

Stopped: “Terminated due to futility”

registry analysis (superiority test); Placebo vs Selepressin Pooled; p = 0.3015; Treatment difference 0.55 (95% CI -1.34 to 2.43); van Elteren test NCT02508649 ↗

paper There were no significant differences in the primary end point (ventilator- and vasopressor-free days: 15.0 vs 14.5 in the selepressin and placebo groups; difference, 0.6 [95% CI, -1.3 to 2.4]; P = .30) PMID 31577035 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject selepressin Protein / enzyme biologic 1.7 unknown Other
Subject selepressin Protein / enzyme biologic 2.5 unknown Other
Subject selepressin Protein / enzyme biologic 3.5 unknown Other
Subject selepressin Protein / enzyme biologic 5 unknown Other