drugset / Trial / NCT00501566

Satavaptan Dose-Ranging Study in Normonatraemic Patients With Cirrhotic Ascites

NCT00501566 ↗

Phase 2 Completed 148 enrolled Sanofi
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective is to determine the optimal dose or range of doses of SR121463B for the treatment of ascites when used concomitantly with a standard dose regimen of spironolactone and furosemide. The secondary objective is to determine the tolerability of different fixed doses of SR121463B over a 14 day treatment period in cirrhotic ascites.

Timeline

Start
2004-04
Primary completion
—
Completion
2005-01

Drugs

EvaluationDrugModalityDoseRoute
Subject satavaptan Small molecule — —

Indications