S47445 15mg
DrugOne 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.
NCT Number: NCT02805439
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.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 2
Mental Health Centre - Plovdiv, Plovdiv, Bulgaria
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Time frame: 8 weeks of treatment
Time frame: at week 0, week 2, week 4, week 6 and week 8
Depressive symptoms
Time frame: at week 0, week 2, week 4, week 6 and week 8
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
Depressive symptoms
Time frame: at week 0, week 2, week 4, week 6 and week 8
Depressive symptoms
Time frame: at week 0, week 2, week 4, week 6 and week 8
Social functioning
Time frame: through study completion (an average of 12 weeks)
Safety criterion
Time frame: at week 4 and week 8
Safety criterion
Time frame: at week 4 and week 8
Safety criterion
Time frame: at week 4 and week 8
Safety criterion
Time frame: at week 4 and week 8
Safety criterion
Time frame: at week 0, week 2, week 4, week 6 and week 8
Safety criterion
Time frame: at week 0, week 2, week 4, week 6 and week 8
Safety criterion
Institut de Recherches Internationales Servier
Other
Efficacy and Safety of S 47445 Versus Placebo as Adjunctive Treatment of Major Depressive Disorder in Patients With an Inadequate Response to Antidepressant Therapy: A Randomised, Double-blind, Placebo Controlled International, Multicentre Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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