Efficacy Study of Vortioxetine (Lu AA21004) for Treatment of Major Depressive Disorder

• ClinicalTrials.gov Identifier: NCT01355081
• Recruitment Status: Completed
• First Posted: May 17, 2011
• Results First Posted: November 11, 2014
• Last Update Posted: November 11, 2014
• Sponsor: Takeda
• Information provided by (Responsible Party): Takeda

Study Description

Brief Summary:

The purpose of this study is to assess the efficacy, safety and tolerability of 8-week treatment with Vortioxetine (Lu AA21004), once daily (QD), in Japanese participants with major depressive disorder.

The purpose of this study is to assess the efficacy, safety and tolerability of 8-week treatment with Lu AA21004, once daily (QD), in Japanese participants with major depressive disorder.

Condition or disease	Intervention/treatment	Phase
Major Depressive Disorder	Drug: Vortioxetine; Drug: Placebo	Phase 3

Detailed Description:

Lu AA21004 was discovered by H. Lundbeck A/S, and is under co-development by H. Lundbeck A/S and Takeda for the treatment of major depressive disorder and general anxiety disorder. Major depressive disorder (MDD) is a chronic, recurring disease with considerable morbidity in the general population. The estimated lifetime prevalence of major depression in the adult population is 5 to 25%, with approximately 2-fold higher prevalence in women than in men. The hallmark of the disease is a depressed mood, with additional symptoms including sleep disturbances, psychomotor agitation or retardation, sexual dysfunction, weight loss, concentration difficulties and delusional ideas. In addition to direct ill effects, MDD causes suicide or job loss and exerts indirect influence on social economy. This study will assess the efficacy and the safety of Lu AA21004. This study consists of a 1-week screening period, an 8-week double-blind treatment period, 4-week safety follow-up.The duration of the study is 13 weeks in total. Blood samples will be collected from participants, and a safety follow-up contact (visit or phone call) will be made 4 weeks after completion of the 8-week double-blind treatment period. Subjects who complete the 8-week double-blind treatment period can successively enter a long-term extension study (Lu AA21004/OCT-001; NCT01395147; hereinafter, OCT-001), if they meet all inclusion criteria and none of exclusion criteria of the OCT-001 study and are willing to participate in the OCT-001 study. Subjects who will enter the OCT-001 will not be requested to safety follow-up after completion of the 8-week double-blind treatment period.

Lu AA21004 was discovered by H. Lundbeck A/S, and is under co-development by H. Lundbeck A/S and Takeda for the treatment of major depressive disorder and general anxiety disorder.

Major depressive disorder (MDD) is a chronic, recurring disease with considerable morbidity in the general population. The estimated lifetime prevalence of major depression in the adult population is 5 to 25%, with approximately 2-fold higher prevalence in women than in men. The hallmark of the disease is a depressed mood, with additional symptoms including sleep disturbances, psychomotor agitation or retardation, sexual dysfunction, weight loss, concentration difficulties and delusional ideas. In addition to direct ill effects, MDD causes suicide or job loss and exerts indirect influence on social economy.

This study will assess the efficacy and the safety of Lu AA21004. This study consists of a 1-week screening period, an 8-week double-blind treatment period, 4-week s safety follow-up.The duration of the study is 13 weeks in total. Blood samples will be collected from participants, and a safety follow-up contact (visit or phone call) will be made 4 weeks after completion of the 8-week double-blind treatment period.

Subjects who complete the 8-week double-blind treatment period can successively enter a long-term extension study (Lu AA21004/OCT-001; NCT01395147; hereinafter, OCT-001), if they meet all inclusion criteria and none of exclusion criteria of the OCT-001 study and are willing to participate in the OCT-001 study.

Subjects who will enter the OCT-001 will not be requested to safety follow-up after completion of the 8-week double-blind treatment period.

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 366 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
• Primary Purpose: Treatment
• Official Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase III Study to Assess the Efficacy and Safety of Lu AA21004 in Patients With Major Depressive Disorder
• Study Start Date: May 2011
• Actual Primary Completion Date: December 2012
• Actual Study Completion Date: December 2012

Arms and Interventions

Arm	Intervention/treatment
Experimental: Vortioxetine 5 mg; Vortioxetine 5 mg, tablets, orally, once daily for up to 8 weeks.	Drug: Vortioxetine; Vortioxetine tablets; Other Names: Lu AA21004; BRINTELLIX
Experimental: Vortioxetine 10 mg; Vortioxetine 10 mg, tablets, orally, once daily for up to 8 weeks.	Drug: Vortioxetine; Vortioxetine tablets; Other Names: Lu AA21004; BRINTELLIX
Placebo Comparator: Placebo; Vortioxetine placebo-matching tablets, orally, once daily for up to 8 weeks.	Drug: Placebo; Vortioxetine placebo; Other Name: Vortioxetine placebo-matching tablets

Outcome Measures

Primary Outcome Measures :

1. Change From Baseline in Montgomery-Åsberg Depression Rating Scale (MADRS) Total Score After 8 Weeks of Treatment [ Time Frame: Baseline, Week 8 ]
   MADRS is a 10-item clinician rated scale that measures overall severity of depressive symptoms (such as apparent sadness, reported sadness, inner tension) rated on a 7-point Likert scale from 0 (symptoms absent) to 6 (severe depression) with a total possible score range from 0 to 60. Higher scores indicate greater severity of symptoms. A negative change from Baseline indicates that symptoms have improved. An analysis of covariance (ANCOVA) model was used with change in MADRS total score as a dependent variable, treatment as a fixed effect and the baseline MADRS total score as a covariate.

Secondary Outcome Measures :

1. Percentage of Patients With MADRS Response After 8 Weeks of Treatment [ Time Frame: Baseline, Week 8 ]
   MADRS is a 10-item clinician rated scale to measure overall severity of depressive symptoms (such as apparent sadness, reported sadness, inner tension) rated on a 7-point Likert scale from 0 (symptoms absent) to 6 (severe depression) with a total possible score range from 0 to 60. Higher scores indicate greater severity of symptoms. Response is defined as a ≥50% decrease in the MADRS Total Score from Baseline.
2. Percentage of Patients With MADRS Remission After 8 Weeks of Treatment [ Time Frame: Week 8 ]
   MADRS is a 10-item clinician rated scale to measure overall severity of depressive symptoms (such as apparent sadness, reported sadness, inner tension) rated on a 7-point Likert scale from 0 (symptoms absent) to 6 (severe depression) with a total possible score range from 0 to 60. Higher scores indicate greater severity of symptoms. Remission is defined as a MADRS Total Score ≤10.
3. Change From Baseline in the Hamilton Depression Scale (HAM-D17) Total Score After 8 Weeks of Treatment [ Time Frame: Baseline, Week 8 ]
   The HAM-D17 is a 17-item rating scale that assesses depressed mood, agitation and somatic symptoms of depression, rated on a 5-point scale from 0 (absent) to 4 (very severe) with a total score range from 0 to 52. Higher scores indicate greater severity of depression symptoms. A negative change from Baseline indicates that symptoms have improved. ANCOVA model was used with treatment as a fixed effect and the baseline HAM-D17 score as a covariate.
4. Clinical Global Impression Scale-Improvement (CGI-I) Score After 8 Weeks of Treatment [ Time Frame: Baseline, Week 8 ]
   The CGI-I assesses the clinician's impression of the participant's state of mental illness improvement and consists of one question for the investigator: "Compared to his condition at the start of the study, how much has this patient changed?" which is rated on a seven-point scale (1=very much improved; 2=much improved; 3=minimally improved; 4=no change from baseline; 5=minimally worse; 6= much worse; 7=very much worse). Higher scores indicate greater severity of illness. Values closest to 1 for this outcome measure indicate the greatest improvement of symptoms. ANCOVA model was used with treatment as a fixed effect and the baseline CGI-Severity (CGI-S) score as a covariate.
5. Change From Baseline in Sheehan Disability Scale (SDS) Total Score After 8 Weeks of Treatment [ Time Frame: Baseline, Week 8 ]
   The SDS is a 3 item rating scale to assess functional impairment (panic, anxiety, phobic and depressive symptoms) over three inter-related domains (work/school, social life, and family life/home responsibilities) rated on an 11 point scale from 0 (not at all) to 10 (extremely) with a total score range from 0 to 30. Higher scores indicate greater severity of impairment. A negative change from Baseline indicates that symptoms have improved. ANCOVA model was used with treatment as a fixed effect and the Baseline SDS total score as a covariate.

Eligibility Criteria

• Ages Eligible for Study: 20 Years to 75 Years (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

1. The subject suffers from Major Depressive Disorder (MDD) as the primary diagnosis according to the Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision (DSM-IV-TR) criteria (classification code 296.2x and 296.3x).
2. The reported duration of the current major depressive episode is at least 3 months at the Screening Visit.
3. The subject has a Montgomery-Åsberg Depression Rating Scale (MADRS) total score ≥26 at the Screening and Baseline Visits.
4. The subject has a Clinical Global Impression Scale-Severity (CGI-S) score ≥4 at the Screening and Baseline Visits

Exclusion Criteria:

1. The subject has one or more of the following conditions:

   • Any current psychiatric disorder other than MDD as defined in the DSM-IV-TR. A subject who exhibits symptoms of anxiety is eligible unless the subject fulfills the diagnostic criteria for a current anxiety disorder per DSM-IV-TR.
   • Current diagnosis or history of manic or hypomanic episode, schizophrenia or any other psychotic disorder, including major depression with psychotic features, mental retardation, organic mental disorders, or mental disorders due to a general medical condition as defined in the DSM-IV-TR.
   • Current diagnosis or history of any substance-related disorder (except nicotine and caffeine-related disorders) as defined in the DSM-IV-TR.
   • Presence or history of a clinically significant neurological disorder (including epilepsy).
   • Neurodegenerative disorder (Alzheimer's disease, Parkinson's disease, multiple sclerosis, Huntington's disease, etc.).
   • Any DSM-IV-TR axis II disorder that might compromise the study.
2. The current depressive symptoms of the subject are considered by the investigator to have been resistant to 2 adequate antidepressant treatments of at least 6 weeks duration each.
3. The subject is at significant risk of suicide or has a score ≥5 on Item 10 (suicidal thoughts) of the MADRS at the Screening and Baseline Visit, or has attempted suicide within 6 months prior to the Screening Visit.

Contacts and Locations

Locations

Japan

Inzai-shi, Chiba, Japan

Noda-City, Chiba, Japan

Fukuoka-city, Fukuoka, Japan

Kitakyushu-shi, Fukuoka, Japan

Annaka-shi, Gunma, Japan

Fujioka-shi, Gunma, Japan

Takasaki-shi, Gunma, Japan

Hatsukaichi-shi, Hiroshima, Japan

Hiroshima-shi, Hiroshima, Japan

Sapporo-Shi, Hokkaido, Japan

Amagasaki-shi, Hyogo, Japan

Kobe-shi, Hyogo, Japan

Fujisawa-shi, Kanagawa, Japan

Kawasaki-shi, Kanagawa, Japan

Sagamihara-shi, Kanagawa, Japan

Yokohama-shi, Kanagawa, Japan

Osaka-shi, Kita-ku, Japan

Kumamoto-shi, Kumamoto, Japan

Kyoto-shi, Kyoto, Japan

Kurashiki-shi, Okayama, Japan

Osaka-shi, Osaka, Japan

Fukaya-shi, Saitama, Japan

Saitama-city, Saitama, Japan

Utsunomiya-shi, Tochigi, Japan

Anan-shi, Tokushima, Japan

Tokushisma-shi, Tokushima, Japan

Hachioji-shi, Tokyo, Japan

Katsushika-ku, Tokyo, Japan

Musashino-shi, Tokyo, Japan

Nanyo-shi, Yamagata, Japan

Ibaraki, Japan

Tokyo, Japan

Sponsors and Collaborators

Takeda

Investigators

• Study Director: Senior Manager; Takeda

More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Inoue T, Nishimura A, Sasai K, Kitagawa T. Randomized, 8-week, double-blind, placebo-controlled trial of vortioxetine in Japanese adults with major depressive disorder, followed by a 52-week open-label extension trial. Psychiatry Clin Neurosci. 2018 Feb;72(2):103-115. doi: 10.1111/pcn.12623. Epub 2017 Dec 27.

• Responsible Party: Takeda
• ClinicalTrials.gov Identifier: NCT01355081
• Other Study ID Numbers: LuAA21004/CCT-003; U1111-1120-9277 ( Registry Identifier: WHO ); JapicCTI-111492 ( Registry Identifier: JapicCTI )
• First Posted: May 17, 2011
• Results First Posted: November 11, 2014
• Last Update Posted: November 11, 2014
• Last Verified: November 2014

Keywords provided by Takeda:

Drug Therapy

Additional relevant MeSH terms:

Depressive Disorder; Depression; Depressive Disorder, Major; Mood Disorders; Mental Disorders; Behavioral Symptoms; Vortioxetine; Antidepressive Agents; Psychotropic Drugs; Anti-Anxiety Agents; Tranquilizing Agents; Central Nervous System Depressants; Physiological Effects of Drugs; Selective Serotonin Reuptake Inhibitors; Neurotransmitter Uptake Inhibitors; Membrane Transport Modulators; Molecular Mechanisms of Pharmacological Action; Neurotransmitter Agents; Serotonin Agents; Serotonin 5-HT1 Receptor Agonists; Serotonin Receptor Agonists; Serotonin 5-HT3 Receptor Antagonists; Serotonin Antagonists