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Completed

NCT Number: NCT02805439

Efficacy and Safety of S 47445 Versus Placebo as Adjunctive Treatment in Depressed Patients Not Fully Recovered From Depressive Symptoms With a Current Antidepressant Treatment

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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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Mental Health Centre - Plovdiv, Plovdiv, Bulgaria

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Outpatients
  • Fulfilling DSM-5 criteria for Major Depressive Disorder confirmed by the brief structured interview M.I.N.I. (single or recurrent episode, current episode ≤ 12 months, current depressive episode of moderate or severe intensity, with or without anxious distress, with or without melancholic features, without mixed features or atypical features, without seasonal pattern, without psychotic features, without catatonic features, without peripartum onset for the current episode)
  • Patients treated for the current depressive episode with an antidepressant treatment with SSRI (fluoxetine, citalopram, paroxetine, escitalopram or sertraline) given in monotherapy at recommended dose for at least 6 weeks and no more than 4 months and with a stable dosage for at least 3 weeks
  • HAM-D total score ≥ 20
  • Clinical Global Impression Severity of illness (item 1): 6 ≥ CGI-S ≥ 4
  • Antidepressant Treatment Response Questionnaire (ATQR) < 50% for the current SSRI
  • Absence of any abnormalities likely to interfere with the conduct of the study (ECG, vital signs, laboratory tests, medical history)

Exclusion criteria

  • Depressive episode of mild intensity according to DSM-5 criteria
  • All types of depressive episodes other than those occurring in a Major Depressive Disorder (Persistent Depressive Disorder (Dysthymia) according to DSM-5 criteria, including persistent depressive disorder with intermittent or persistent major depressive episode according to DSM-5, Premenstrual Dysphoric Disorder, Substance Induced Depressive Disorder, Depressive Disorder due to another Medical Condition, Other Specified or Unspecified Depressive Disorder, Bipolar Disorder I or II, depressed episode, Schizoaffective Disorder (Depressive or Bipolar type))
  • Depression onset within 12 months after a stroke
  • Suicidal risk defined as a score > 3 on the item 3 of the HAM-D scale or in the investigator's opinion
  • Lactose intolerance
  • Patients with hereditary problems of galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption
  • Resistant depression for the current episode (patients who have not responded to 1 previous antidepressant treatment before the SSRI taken at an appropriate dose)
  • Current panic disorder
  • Obsessive compulsive disorder
  • Current post traumatic stress disorder, current acute stress disorder
  • Current or past psychotic disorder
  • Any severe personality features

Treatment and study plan

S47445 15mg

Drug

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.

S47445 50mg

Drug

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.

Placebo

Drug

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.

Primary outcomes

  1. Hamilton Depression Rating Scale (HAM-D) total score expressed as change from baseline value

    Time frame: 8 weeks of treatment

Secondary outcomes

  1. HAM-D total score

    Time frame: at week 0, week 2, week 4, week 6 and week 8

    Depressive symptoms

  2. Response to treatment defined by HAM-D total score decrease from baseline ≥ 50%

    Time frame: at week 0, week 2, week 4, week 6 and week 8

    Depressive symptoms

  3. 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)

    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

  4. Hospital Anxiety and Depression Scale (HAD), Anxiety and Depression sub-scores

    Time frame: at week 0, week 2, week 4, week 6 and week 8

    Depressive symptoms

  5. Sheehan Disability Scale (SDS) scores (Work, social and family life)

    Time frame: at week 0, week 2, week 4, week 6 and week 8

    Social functioning

  6. Adverse Events

    Time frame: through study completion (an average of 12 weeks)

    Safety criterion

  7. Body Weight

    Time frame: at week 4 and week 8

    Safety criterion

  8. BMI

    Time frame: at week 4 and week 8

    Safety criterion

  9. Laboratory tests (haematology and biochemistry)

    Time frame: at week 4 and week 8

    Safety criterion

  10. 12-lead ECG

    Time frame: at week 4 and week 8

    Safety criterion

  11. Vital signs (standing and supine Systolic and Diastolic Blood Pressure, heart rate)

    Time frame: at week 0, week 2, week 4, week 6 and week 8

    Safety criterion

  12. Columbia-Suicide Severity Rating Scale (C-SSRS)

    Time frame: at week 0, week 2, week 4, week 6 and week 8

    Safety criterion

Sponsors and collaborators

Lead sponsor

Institut de Recherches Internationales Servier

Other

Collaborators

  • ADIR Association

Registry information

Official study title

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

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Jun 20, 2016
Registry last updated
Jan 3, 2020

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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