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Ocelot Bio’s lead candidate, OCE-205, has shown activity and safety in Phase 1 clinical trials and is currently in Phase 2 for hepatorenal syndrome with acute kidney injury (HRS-AKI). The FDA has granted OCE-205 Orphan Drug Designation for this indication. A second program for ascites is in preclinical development. Data presented at AASLD demonstrated pharmacodynamic activity and safety in healthy volunteers[5][7].
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