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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