drugset / Trial / NCT01436500

Safety and Pharmacokinetics of Ifetroban in Hepatorenal Syndrome Patients

NCT01436500 ↗

Phase 2 Completed 55 enrolled Cumberland Pharmaceuticals
RandomizedParallel-groupTriple-blindTreatment

Summary

A study of ifetroban in the treatment of hepatorenal syndrome (HRS) in hospitalized adult patients to assess the safety and pharmacokinetics of 3 days of intravenous ifetroban.

Timeline

Start
2011-10
Primary completion
2015-06
Completion
2015-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Ifetroban Small molecule 5 mg Intravenous
Subject Ifetroban Small molecule 15 mg Intravenous
Subject Ifetroban Small molecule 50 mg Intravenous
Subject Ifetroban Small molecule 150 mg Intravenous

Indications