drugset / Trial / NCT01143246

A Placebo-Controlled, Double-Blind Study to Confirm the Reversal of Hepatorenal Syndrome Type 1 With Terlipressin

NCT01143246 ↗

Phase 3 Completed 196 enrolled Mallinckrodt
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is designed to evaluate the efficacy and safety of intravenous terlipressin versus placebo for the treatment of type 1 hepatorenal syndrome (HRS) in participants receiving standard of care albumin therapy.

Timeline

Start
2010-10-11
Primary completion
2013-02
Completion
2013-05-10

Outcome

Missed primary endpoint

paper CHRSR was observed in 19 of 97 patients (19.6%) receiving terlipressin vs 13 of 99 patients (13.1%) receiving placebo (P = .22). PMID 26896734 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Terlipressin Peptide 1 mg Intravenous

Indications