The purpose of this study is to assess the efficacy and safety of S47445 versus placebo as adjunctive treatment of Major Depressive Disorder in patients with an inadequate response to antidepressant therapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
400
One tablet of S47445 15 mg taken orally once a day during breakfast concomitantly to the current selective serotonin reuptake inhibitor treatment, starting the day after inclusion visit and ending the day of the W8 visit.
One tablet of S47445 50 mg taken orally once a day during breakfast concomitantly to the current selective serotonin reuptake inhibitor treatment, starting the day after inclusion visit and ending the day of the W8 visit.
One tablet of placebo taken orally once a day during breakfast concomitantly to the current selective serotonin reuptake inhibitor treatment, starting the day after inclusion visit and ending the day of the W8 visit.
Hamilton Depression Rating Scale (HAM-D) total score expressed as change from baseline value
Time frame: 8 weeks of treatment
HAM-D total score
Depressive symptoms
Time frame: at week 0, week 2, week 4, week 6 and week 8
Response to treatment defined by HAM-D total score decrease from baseline ≥ 50%
Depressive symptoms
Time frame: at week 0, week 2, week 4, week 6 and week 8
Clinical Global Impression scale (CGI), item 1 (Severity of depression) and item 2 (global Improvement) scores, response to treatment (CGI item 2 = 1 or 2)
Depressive symptoms
Time frame: CGI item 1 at week 0, week 2, week 4, week 6 and week 8 and item 2 at week 2, week 4, week 6 and week 8
Hospital Anxiety and Depression Scale (HAD), Anxiety and Depression sub-scores
Depressive symptoms
Time frame: at week 0, week 2, week 4, week 6 and week 8
Sheehan Disability Scale (SDS) scores (Work, social and family life)
Social functioning
Time frame: at week 0, week 2, week 4, week 6 and week 8
Adverse Events
Safety criterion
Time frame: through study completion (an average of 12 weeks)
Body Weight
Safety criterion
Time frame: at week 4 and week 8
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Mental Health Centre - Plovdiv
Plovdiv, Bulgaria
Mental Health Centre - Sofia district
Sofia, Bulgaria
Military Medical Academy, MHAT - Sofia
Sofia, Bulgaria
Diagnostic Consultative center "Tchaika"
Varna, Bulgaria
Medical center "City clinic"
Varna, Bulgaria
Mental health centre - Vratsa
Vratsa, Bulgaria
Saint Anne s.r.o.
Brno, Czechia
Soukroma psychiatricka ambulance
Brno, Czechia
Neuropsychiatrie HK, s.r.o.
Hradec Králové, Czechia
Bialbi s.r.o.
Litoměřice, Czechia
...and 43 more locations
BMI
Safety criterion
Time frame: at week 4 and week 8
Laboratory tests (haematology and biochemistry)
Safety criterion
Time frame: at week 4 and week 8
12-lead ECG
Safety criterion
Time frame: at week 4 and week 8
Vital signs (standing and supine Systolic and Diastolic Blood Pressure, heart rate)
Safety criterion
Time frame: at week 0, week 2, week 4, week 6 and week 8
Columbia-Suicide Severity Rating Scale (C-SSRS)
Safety criterion
Time frame: at week 0, week 2, week 4, week 6 and week 8