Major Depressive Disorders Clinical Trial
Official title:
A Fifty-Two-Week Multicenter, Open-Label, Study Evaluating the Long-Term Safety and Tolerability of SR58611A 350 mg q12 in Patients With Major Depressive Disorder.
Primary objective:
- To evaluate the long-term safety and tolerability of SR58611A (amibegron) patients with
major depressive disorder (MDD).
Secondary objective:
- To determine plasma concentrations of SR58878 (the active metabolite of SR58611A), for
pharmacokinetic population analyses, to evaluate the quality of life (QoL) in patients with
MDD, and to evaluate the efficacy of amibegron in patients with MDD.
n/a
Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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