drugset / Trial / NCT04112199

A Study for Evaluation of BIV201 to Reduce Ascites and Complications in Patients With Cirrhosis and Refractory Ascites

NCT04112199 ↗

Phase 2 Terminated 15 enrolled BioVie Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

This study evaluates the addition of BIV201 (terlipressin diacetate) as a continuous infusion in addition to standard of care (diuretics and therapeutic paracentesis) for reduction of ascites and complications in adult patients with refractory ascites secondary to decompensated cirrhosis

Timeline

Start
2021-06-17
Primary completion
2023-05-08
Completion
2023-05-08

Outcome

Outcome not reported

Stopped: “For reasons unrelated to safety or efficacy”

Drugs

EvaluationDrugModalityDoseRoute
Subject BIV201 Unknown 8 mg —

Indications