A MULTI-CENTER, RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND, ADAPTIVE DOSE RANGING STUDY TO ASSESS SAFETY AND EFFICACY OF INTRAVENOUS OCE-205 IN ADULTS DIAGNOSED WITH CIRRHOSIS WITH ASCITES WHO HAVE DEVELOPED HEPATORENAL SYNDROME ACUTE KIDNEY INJURY (HRS-AKI)

Registry ID
OCE-205-201
Source registry
HEALTH_CANADA
Status
Closed
Study type
INTERVENTIONAL
Sponsor
OCELOT BIO, INC.
Start date
2023-05-12
Completion date
2023-07-04
Last update
2022-04-07

Conditions

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