Winst gevend schreef op 15 maart 2021 16:17:
RemdesivirThe Kaplan–Meier estimates of mortality were 6.7% with remdesivir
and 11.9% with placebo by day 15
and 11.4% with remdesivir
and 15.2% with placebo by day 29 (hazard ratio, 0.73; 95% CI, 0.52 to 1.03).
Serious adverse events were reported in
131 of the 532 patients who received remdesivir (24.6%) and in
163 of the 516 patients who received placebo (31.6%).
Conestat AlfaUnknown: in trials along with SOC Remdesivir.
trialsjournal.biomedcentral.com/artic...(the Switserland/Mexico and Brasil trials)