This clinical trial is focused on studying cirrhosis, a condition where the liver becomes scarred and damaged. The study will evaluate the safety of two medications, Zibotentan and Dapagliflozin, both individually and in combination. Zibotentan is taken as a hard capsule, while Dapagliflozin is a film-coated tablet. The trial will also include a comparison with a placebo. The purpose of the study is to understand how these treatments affect fluid retention, body weight, and blood pressure in people with cirrhosis.
Participants in the study will receive either the combination of Zibotentan and Dapagliflozin, Zibotentan alone, or a placebo. The study will last for a period of six weeks, during which the effects of the treatments on body weight, body water volumes, and blood pressure will be monitored. The trial aims to see if the combination of medications can better manage symptoms compared to taking Zibotentan alone or a placebo.
Throughout the study, participants will be closely monitored for any changes in their condition, including any side effects or adverse events. The trial will help determine the safety and effectiveness of using Zibotentan and Dapagliflozin together for treating cirrhosis. This research could provide valuable insights into new treatment options for managing this liver condition.



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