4 results
Approved WMOWill not start
The objective of the study is to evaluate various doses of SSR125543 in first patients (outpatients with a major depressive disorder), evaluate collected information concerning tolerability, efficacy en safety. The same infomation will be evaluated…
Approved WMOCompleted
Investigating the bioequivalence of the new formulation of escitalopram.
Approved WMOCompleted
Observe the adherence rate of antidepressants during pregnancy and secondary exploration of possible factors which contribute to non-adherence
Approved WMOCompleted
Investigating the bioequivalence of the new formulation of escitalopram.