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Open-label, Flexible-dose Study of Vortioxetine in Patients With Depression in India

Open-label, Flexible-dose Study of Vortioxetine in Patients With Major Depressive Disorder in India

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04288895
Enrollment
400
Registered
2020-02-28
Start date
2020-02-20
Completion date
2022-03-12
Last updated
2022-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Major Depressive Disorder

Brief summary

The purpose of this study is to evaluate the safety and tolerability of flexible doses of vortioxetine (5 - 20 mg/day) over a period of 12 weeks in patients with depression in India

Interventions

DRUGVortioxetine

5 - 20 mg/day flexible-dose vortioxetine, tablets, orally

Sponsors

H. Lundbeck A/S
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* The patient has a Major Depressive Episode (MDE), is diagnosed with Major Depressive Disorder (MDD) according to DSM-5® and would benefit from pharmacological treatment with vortioxetine. The current MDE should be confirmed using the Mini International Neuropsychiatric Interview (MINI). * The patient has a CGI-S ≥4 at screening.

Exclusion criteria

* The patient has a significant risk of suicide according to investigator's clinical judgment or has made an actual suicide attempt in the period of 6 months prior to screening. * The patient previously received vortioxetine. Other in- and

Design outcomes

Primary

MeasureTime frame
Number of participants with Treatment-Emergent Adverse EventsFrom baseline to week 12

Secondary

MeasureTime frameDescription
Clinical Global Impression-improvement (CGI-I)At week 12The CGI was developed to provide global measures of the severity of a patient's clinical condition and improvement or worsening during clinical studies. The CGI consists of two clinician-rated subscales: severity of illness (CGI-S) and global improvement (CGI-I). The CGI-I provides the clinician's impression of the patient's improvement (or worsening). The clinician assesses the patient's condition relative to a baseline on a 7-point scale ranging from 1 (very much improved) to 7 (very much worse).
Change in Patient Health Questionnaire-9 (PHQ-9) total scoreFrom baseline to week 12The PHQ-9 is a patient-rated scale designed to screen for and assess depression. The PHQ-9 consists of questions on each of the 9 DSM-5® criteria for depression asking if they have bothered the patient over the last 2 weeks. Each question is rated on a scale from 0 (not at all) to 3 (nearly every day). The 9 questions are summed to a total score ranging from 0 to 27 with higher scores reflecting greater severity.
Change in Clinical Global Impression-severity of illness (CGI-S) scoreFrom baseline to week 12The CGI was developed to provide global measures of the severity of a patient's clinical condition and improvement or worsening during clinical studies. The CGI consists of two clinician-rated subscales: severity of illness (CGI-S) and global improvement (CGI-I). The CGI-S provides the clinician's impression of the patient's current state of mental illness. The clinician uses his or her clinical experience of this patient population to rate the severity of the patient's current mental illness on a 7-point scale ranging from 1 (normal - not at all ill) to 7 (among the most extremely ill patients).

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026