RANDOMISED, DOUBLE-BLIND, PLACEBO-CONTROLLED AND PARALLEL GROUP TRIAL TO INVESTIGATE THE EFFECTS OF ONE DOSE (UP-TITRATION TO A FIXED DOSE REGIMEN) OF ORAL BI 685509 ON PORTAL HYPERTENSION AFTER 8 WEEKS TREATMENT IN PATIENTS WITH CLINICALLY SIGNIFICANT PORTAL HYPERTENSION (CSPH) IN DECOMPENSATED CIRRHOSIS AFTER THEIR FIRST DECOMPENSATION EVENT, WHO ARE STABILIZED CTP 5-7, PHASE II

Registry ID
1366-0055
Source registry
HEALTH_CANADA
Status
Closed
Phase
PHASE2
Study type
INTERVENTIONAL
Sponsor
BOEHRINGER INGELHEIM (CANADA) LTD LTEE
Completion date
2024-05-09
Last update
2023-09-25

Conditions

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