drugset / Trial / NCT04112199
A Study for Evaluation of BIV201 to Reduce Ascites and Complications in Patients With Cirrhosis and Refractory Ascites
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | BIV201 | Unknown | 8 mg | — |