3 results
Primary objective:To determine the response to a 144-hour (6 day) continuous intravenous infusion of SAGE-547 compared to placebo administered to support the weaning of all third-line agents in subjects with SRSE, and for the response to endure at…
The aim of the study is, to analyze the effect of the haemoadsorption device Cytosorb in relation to the inflammatory parameters IL-6, IL-8, IL-10,TNF-* and CRP at six different time points during conventional CABG procedures.We assess whether the…
The primary objective of the trial is to demonstrate non-inferiority of treatment with TMC278 when administered as 75 mg q.d. compared to the control group (EFV) in regard to the proportion of virologic responders (plasma viral load < 50 HIV-…