A Study of Esketamine Nasal Spray Versus Placebo Spray in Adult Participants With Treatment-resistant Depression
A Randomized, Double-blind, Multicenter, Placebo-controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Esketamine Nasal Spray, Administered as Monotherapy, in Adult Participants With Treatment-resistant Depression
The purpose of this study is to evaluate how well each individual dose of esketamine (56 milligrams [mg] and 84 mg) works when compared with placebo in improving depressive symptoms in participants with treatment resistant depression (individuals with major depressive disorder [MDD] who have not responded to at least 2 different antidepressant treatments given at an adequate dose for an adequate duration in the current episode of depression).
Studienübersicht
Status
Status
Bedingungen
Bedingungen
Intervention / Behandlung
Intervention / Behandlung
Studientyp
Studientyp
Einschreibung (Geschätzt)
Einschreibung
Phase
Phase
- Phase 3
Kontakte und Standorte
Studienkontakt
Studienkontakt
- Name: Study Contact
- Telefonnummer: 844-434-4210
- E-Mail: Participate-In-This-Study1@its.jnj.com
Studienorte
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Beijing, China, 100088
- Rekrutierung
- Beijing Anding Hospital of Capital Medical University
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Beijing, China, 102208
- Rekrutierung
- Beijing Huilongguan Hospital
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Wuhu, China, 242407
- Rekrutierung
- Wuhu Hospital of Beijing Anding hospital
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Akita, Japan, 010 0921
- Rekrutierung
- Heart Care Clinic Omachi
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Karatsu, Japan, 847-0031
- Rekrutierung
- Rainbow & Sea Hospital
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Kawasaki, Japan, 214-0014
- Rekrutierung
- Kishiro Mental Clinic
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Kobe, Japan, 651-0097
- Rekrutierung
- Tatsuta Clinic
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Kodaira, Japan, 187-8551
- Rekrutierung
- National Center of Neurology and Psychiatry
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Koshigaya, Japan, 343-0032
- Rekrutierung
- Juntendo University Koshigaya Hospital
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Maebashi, Japan, 371-0031
- Rekrutierung
- Ichikawa Clinic
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Minatoku, Japan, 105-8471
- Rekrutierung
- The Jikei University Hospital
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Mitaka, Japan, 181-8611
- Rekrutierung
- Kyorin University Hospital
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Miyakonojō, Japan, 885-0093
- Rekrutierung
- Miyakonojo Shinsei Hospital
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Nagasaki, Japan, 852-8137
- Rekrutierung
- Arata Clinic
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Sapporo, Japan, 060 8648
- Rekrutierung
- Hokkaido University Hospital
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Setagaya-ku/Tokyo, Japan, 154 0004
- Rekrutierung
- Sangenjaya neurology-psychosomatic clinic
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Shibuya Tokyo, Japan, 151-0053
- Rekrutierung
- Maynds Tower Mental Clinic
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Tottori, Japan, 683-0824
- Rekrutierung
- Tottori University Hospital
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Kaohsiung City, Taiwan, 80756
- Rekrutierung
- Kaohsiung Medical University Chung Ho Memorial Hospital
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Taichung, Taiwan, 402
- Rekrutierung
- Chung Shan Medical University Hospital
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Tainan, Taiwan, 704
- Rekrutierung
- National Cheng Kung University Hospital
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Taipei, Taiwan, 11217
- Rekrutierung
- Taipei Veterans General Hospital
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Taipei, Taiwan, 110
- Rekrutierung
- Taipei Medical University
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Taoyuan, Taiwan, 333
- Rekrutierung
- Linkou Chang Gung Memorial Hospital
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California
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Redlands, California, Vereinigte Staaten, 92374
- Rekrutierung
- Anderson Clinical Research
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San Diego, California, Vereinigte Staaten, 92123
- Rekrutierung
- Artemis Institute for Clinical Research
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Connecticut
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Farmington, Connecticut, Vereinigte Staaten, 06032
- Rekrutierung
- University of Connecticut Health Center
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Florida
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Cape Coral, Florida, Vereinigte Staaten, 33909
- Rekrutierung
- American Family Research Group
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Miami, Florida, Vereinigte Staaten, 33126
- Rekrutierung
- Pharmax Research Clinic Inc
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Orlando, Florida, Vereinigte Staaten, 32803
- Rekrutierung
- Charter Research Orlando
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Georgia
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Marietta, Georgia, Vereinigte Staaten, 30060
- Rekrutierung
- Psych Atlanta, P.C.
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Snellville, Georgia, Vereinigte Staaten, 30078
- Rekrutierung
- Accelerated Clinical Research Group LLC
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Idaho
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Saint Maries, Idaho, Vereinigte Staaten, 63304
- Rekrutierung
- Midwest Research Group
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Illinois
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Skokie, Illinois, Vereinigte Staaten, 60076
- Rekrutierung
- Psychiatric Medicine Associates LLC
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Massachusetts
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Watertown, Massachusetts, Vereinigte Staaten, 02472
- Rekrutierung
- Adams Clinical Watertown
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New York
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Cedarhurst, New York, Vereinigte Staaten, 11516
- Rekrutierung
- Neurobehavioral Research Inc
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New York, New York, Vereinigte Staaten, 10128
- Rekrutierung
- The Medical Research Network, LLC
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Ohio
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Columbus, Ohio, Vereinigte Staaten, 43210
- Rekrutierung
- Ohio State University
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Washington
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Bellevue, Washington, Vereinigte Staaten, 98007
- Rekrutierung
- Northwest Clinical Research Center
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Teilnahmekriterien
Zulassungskriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Participant must meet the diagnostic and statistical manual of mental disorders (5th edition) (DSM-5) diagnostic criteria for single-episode major depressive disorder (MDD) (if single episode MDD, the duration of the episode must be greater than or equal to [>=] 12 months) or recurrent MDD, without psychotic features, based upon clinical assessment and confirmed by the mini international neuropsychiatric interview (MINI) as the primary diagnosis. Participant must have had the first onset of depression prior to 55 years of age
- Participant must have had nonresponse (less than or equal to [<=] 25 percent [%] improvement) to >=2 oral antidepressant treatments in the current episode of depression, assessed using the massachusetts general hospital-antidepressant treatment response questionnaire (MGH-ATRQ), and confirmed by documented records (for example, medical/pharmacy/prescription records or a letter from a treating physician)
- The participant's current major depressive episode, depression symptom severity, and antidepressant treatment response in the current depressive episode, must be confirmed by the state versus trait, assessability, face validity, ecological validity, rule of three P's (SAFER) Interview
- Participant must be comfortable with self-administration of nasal spray medication and be able to follow the nasal spray administration instructions provided
- A female participant of childbearing potential must have a negative highly sensitive serum (β-human chorionic gonadotropin [β-hCG]) at the start of screening and a negative urine pregnancy test must be obtained before the first dose of study drug on Day 1, prior to randomization
Exclusion Criteria:
- The participant has used ketamine/esketamine (lifetime)
- The participant's depressive symptoms have demonstrated nonresponse in the current major depressive episode to an adequate course of treatment with electroconvulsive therapy (ECT), defined as at least 7 treatments with unilateral/bilateral ECT, or to adequate course of treatment with transcranial magnetic stimulation (TMS), defined as at least 4 weeks of treatment with 5 sessions per week
- Participant has received vagal nerve stimulation (VNS) or deep brain stimulation (DBS) in the current episode of depression
- Participant has homicidal ideation/intent, per the investigator's clinical judgment, or has suicidal ideation with some intent to act within 6 months prior to the start of the screening phase, per the investigator's clinical judgment or based on the columbia suicide severity rating scale (C-SSRS), corresponding to a response of "Yes" on Item 4 (active suicidal ideation with some intent to act, without specific plan) or Item 5 (active suicidal ideation with specific plan and intent) for suicidal ideation on the C-SSRS, or a history of suicidal behavior within the past year prior to the start of the screening phase. Participants reporting suicidal ideation with intent to act or suicidal behavior prior to the start of the double-blind treatment phase should be excluded
- Participant has a history of moderate or severe substance or alcohol use disorder according to DSM-5 criteria, except nicotine or caffeine, within 6 months before the start of the screening phase. a. A history (lifetime) of ketamine, phencyclidine (PCP), lysergic acid diethylamide (LSD), or 3, 4-methylenedioxy-methamphetamine (MDMA) hallucinogen-related use disorder is exclusionary
- Participant has a current or history of seizures (uncomplicated childhood febrile seizures with no sequelae are not exclusionary)
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Doppelt
Anzahl der Arme
Waffen und Interventionen
Teilnehmergruppe / ArmTeilnehmergruppe / Arm |
Intervention / BehandlungIntervention / Behandlung |
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Experimental: Esketamine 56 milligram (mg)
Participants will be randomized to receive double-blind (DB) treatment with esketamine 56 mg, twice a week for 4 weeks. Participants who complete the DB treatment phase on Day 28 may be eligible to participate in an open-label treatment phase and receive either esketamine 56 or 84 mg. |
Participants will self-administer 56 mg of esketamine as intranasal spray into each nostril.
Andere Namen:
Participants will self-administer 84 mg of esketamine as intranasal spray into each nostril.
Andere Namen:
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Experimental: Esketamine 84 mg
Participants will be randomized to receive DB treatment with esketamine 84 mg, twice a week for 4 weeks. Participants who complete the DB treatment phase on Day 28 may be eligible to participate in an open-label treatment phase and receive either esketamine 56 or 84 mg. |
Participants will self-administer 56 mg of esketamine as intranasal spray into each nostril.
Andere Namen:
Participants will self-administer 84 mg of esketamine as intranasal spray into each nostril.
Andere Namen:
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Placebo-Komparator: Placebo
Participants will be randomized to receive DB treatment with placebo twice a week for 4 weeks. Participants who complete the DB treatment phase on Day 28 may be eligible to participate in an open-label treatment phase and receive either esketamine 56 mg or 84 mg. |
Participants will self-administer 56 mg of esketamine as intranasal spray into each nostril.
Andere Namen:
Participants will self-administer 84 mg of esketamine as intranasal spray into each nostril.
Andere Namen:
Participants will self-administer placebo as intranasal spray into each nostril. |
Was misst die Studie?
Primäre Ergebnismessungen
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Double-Blind (DB) Treatment Phase: Change From Baseline in Montgomery-Asberg Depression Rating Scale (MADRS) Total Score From Day 1 to the End of the 4-Week Double-Blind Treatment Phase
Zeitfenster: Baseline (Day 1 [prerandomization]) up to end of the 4-Week DB treatment phase (Day 28)
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The MADRS is a clinician-rated scale designed to measure depression severity and detects changes due to antidepressant treatment. The scale consists of 10 items, each of which is scored from 0 (item not present or normal) to 6 (severe or continuous presence of the symptoms), for a total possible score of 60. Higher scores represent a more severe condition. |
Baseline (Day 1 [prerandomization]) up to end of the 4-Week DB treatment phase (Day 28)
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Sekundäre Ergebnismessungen
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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DB Treatment Phase: Change From Baseline in MADRS Total Score From Day 1 to Day 2
Zeitfenster: Baseline (Day 1 [prerandomization]) up to Day 2 (approximately 24 hours after the first dose)
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The MADRS is a clinician-rated scale designed to measure depression severity and detects changes due to antidepressant treatment. The scale consists of 10 items, each of which is scored from 0 (item not present or normal) to 6 (severe or continuous presence of the symptoms), for a total possible score of 60. Higher scores represent a more severe condition. |
Baseline (Day 1 [prerandomization]) up to Day 2 (approximately 24 hours after the first dose)
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DB Treatment Phase: Percentage of Responders in MADRS Over Time to the End of the 4-Week DB Treatment Phase
Zeitfenster: Up to end of the 4-Week DB treatment phase (Day 28)
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Percentage of responders (greater than or equal to [>=] 50 percent [%] reduction from baseline in MADRS total score) over time to the end of the 4-week DB treatment phase will be reported. The MADRS is a clinician-rated scale designed to measure depression severity and detects changes due to antidepressant treatment. The scale consists of 10 items, each of which is scored from 0 (item not present or normal) to 6 (severe or continuous presence of the symptoms), for a total possible score of 60. Higher scores represent a more severe condition. |
Up to end of the 4-Week DB treatment phase (Day 28)
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DB Treatment Phase: Percentage of Participants in Remission in MADRS Over Time to the End of the 4-Week DB Treatment Phase
Zeitfenster: Up to end of the 4-Week DB treatment phase (Day 28)
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Percentage of participants in remission (MADRS less than or equal to [<=] 10 and MADRS <= 12) over time to the end of the 4-week DB treatment phase will be reported. The MADRS is a clinician-rated scale designed to measure depression severity and detects changes due to antidepressant treatment. The scale consists of 10 items, each of which is scored from 0 (item not present or normal) to 6 (severe or continuous presence of the symptoms), for a total possible score of 60. Higher scores represent a more severe condition. |
Up to end of the 4-Week DB treatment phase (Day 28)
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DB Treatment Phase: Change From Baseline in Clinical Global Impression-Severity (CGI-S) Over Time to the End of the 4-Week DB Treatment Phase
Zeitfenster: Baseline up to end of the 4-Week DB treatment phase (Day 28)
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Change from baseline in CGI-S over time to the end of the 4-week DB treatment phase will be reported. The CGI-S is a clinician-rated scale that measures illness severity. The CGI has proved to be a robust measure of efficacy in many clinical drug trials and is easy and quick to administer. The CGI-S is rated on a 7-point scale, with the severity of illness scale using a range of responses from 1 (normal) through to 7 (among the most severely ill participants). |
Baseline up to end of the 4-Week DB treatment phase (Day 28)
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DB Treatment Phase: Change From Baseline in MADRS Total Score Over Time to the End of the 4-Week DB Treatment Phase
Zeitfenster: Baseline up to end of the 4-Week DB treatment phase (Day 28)
|
Change from baseline in MADRS total score over time to the end of the 4-week DB treatment phase will be reported. The MADRS is a clinician-rated scale designed to measure depression severity and detects changes due to antidepressant treatment. The scale consists of 10 items, each of which is scored from 0 (item not present or normal) to 6 (severe or continuous presence of the symptoms), for a total possible score of 60. Higher scores represent a more severe condition. |
Baseline up to end of the 4-Week DB treatment phase (Day 28)
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DB Treatment Phase: Change From Baseline in Individual MADRS Item Scores Over Time to the End of the 4-Week DB Treatment Phase
Zeitfenster: Baseline up to end of the 4-Week DB treatment phase (Day 28)
|
Change from baseline in individual MADRS item scores over time to the end of the 4-week DB treatment phase will be reported. The MADRS is a clinician-rated scale designed to measure depression severity and detects changes due to antidepressant treatment. The scale consists of 10 items, each of which is scored from 0 (item not present or normal) to 6 (severe or continuous presence of the symptoms), for a total possible score of 60. Higher scores represent a more severe condition. |
Baseline up to end of the 4-Week DB treatment phase (Day 28)
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DB Treatment Phase: Change From Baseline in Anhedonia Symptoms Over Time to the End of the 4-Week DB Treatment Phase As Assessed by MADRS Anhedonia Factor Score
Zeitfenster: Baseline up to end of the 4-Week DB treatment phase (Day 28)
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Change from baseline in anhedonia symptoms over time to the end of the 4-week DB treatment phase as assessed by MADRS anhedonia factor score will be reported. The MADRS anhedonia factor is a widely used 5-item subscale of the MADRS used to specifically measure the lack of pleasure (anhedonia) in depression, combining items for apparent sadness, reported sadness, concentration difficulties, lassitude (tiredness), and inability to feel. The sum of these five items (each scored 0-6), resulting in a score from 0 to 30, with higher scores indicating more severe anhedonia. This score helps assess treatment effectiveness for anhedonia, correlates with functional improvement, and provides a deeper look beyond the total depression score, showing significant clinical relevance in major depressive disorder (MDD) trials. |
Baseline up to end of the 4-Week DB treatment phase (Day 28)
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DB Treatment Phase: Change From Baseline in Patient-Reported Anhedonia Symptoms Over Time to the End of the 4-Week DB Treatment Phase As Assessed by Patient Health Questionnaire 9-item (PHQ-9) Item 1 Score
Zeitfenster: Baseline up to end of the 4-Week DB treatment phase (Day 28)
|
Change from baseline in patient-reported anhedonia symptoms over time to the end of the 4-week DB treatment phase as assessed by PHQ-9 item 1 score (little interest/pleasure in things) will be reported. The PHQ-9 is a participant-reported outcome measure that will be used to assess depressive symptoms. The scale scores each of the 9 symptom domains of the diagnostic and statistical manual of mental disorders (5th edition) (DSM-5) MDD criteria and it has been used both as a screening tool and a measure of response to treatment for depression. Each item is rated on a 4-point scale (0=not at all, 1=several days, 2=more than half the days, and 3=nearly every day). |
Baseline up to end of the 4-Week DB treatment phase (Day 28)
|
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DB Treatment Phase: Change From Baseline in PHQ-9 Total Score Over Time to the End of the 4-Week DB Treatment Phase
Zeitfenster: Baseline up to end of the 4-Week DB treatment phase (Day 28)
|
Change from baseline in PHQ-9 total score over time to the end of the 4-week DB treatment phase will be reported. The PHQ-9 is a participant-reported outcome measure that will be used to assess depressive symptoms. The scale scores each of the 9 symptom domains of the DSM-5 MDD criteria and it has been used both as a screening tool and a measure of response to treatment for depression. Each item is rated on a 4-point scale (0=not at all, 1=several days, 2=more than half the days, and 3=nearly every day). The participant's item responses are summed to provide a total score (range of 0 to 27) with higher scores indicating greater severity of depressive symptoms. |
Baseline up to end of the 4-Week DB treatment phase (Day 28)
|
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DB Treatment Phase: Percentage of Responders in PHQ-9 Over Time to the End of the 4-Week DB Treatment Phase
Zeitfenster: Up to end of the 4-Week DB treatment phase (Day 28)
|
Percentage of responders (>= 50% reduction from baseline in PHQ-9 total score) over time to the end of the 4-week DB treatment phase will be reported. The PHQ-9 is a participant-reported outcome measure that will be used to assess depressive symptoms. The scale scores each of the 9 symptom domains of the DSM-5 MDD criteria and it has been used both as a screening tool and a measure of response to treatment for depression. Each item is rated on a 4-point scale (0=not at all, 1=several days, 2=more than half the days, and 3=nearly every day). The participant's item responses are summed to provide a total score (range of 0 to 27) with higher scores indicating greater severity of depressive symptoms. |
Up to end of the 4-Week DB treatment phase (Day 28)
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DB Treatment Phase: Percentage of Participants in Remission in PHQ-9 Over Time to the End of the 4-Week DB Treatment Phase
Zeitfenster: Up to end of the 4-Week DB treatment phase (Day 28)
|
Percentage of participants in remission (PHQ-9 total score < 5) over time to the end of the 4-week DB treatment phase will be reported. The PHQ-9 is a participant-reported outcome measure that will be used to assess depressive symptoms. The scale scores each of the 9 symptom domains of the DSM-5 MDD criteria and it has been used both as a screening tool and a measure of response to treatment for depression. Each item is rated on a 4-point scale (0=not at all, 1=several days, 2=more than half the days, and 3=nearly every day). The participant's item responses are summed to provide a total score (range of 0 to 27) with higher scores indicating greater severity of depressive symptoms. |
Up to end of the 4-Week DB treatment phase (Day 28)
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Open-Label (OL) Treatment Phase: Percentage of Responders in MADRS Over Time to the End of the OL Treatment Phase
Zeitfenster: Up to 12 Weeks
|
Percentage of responders (>= 50% reduction from baseline in MADRS total score) over time to the end of the OL treatment phase will be reported. The MADRS is a clinician-rated scale designed to measure depression severity and detects changes due to antidepressant treatment. The scale consists of 10 items, each of which is scored from 0 (item not present or normal) to 6 (severe or continuous presence of the symptoms), for a total possible score of 60. Higher scores represent a more severe condition. |
Up to 12 Weeks
|
|
OL Treatment Phase: Percentage of Participants in Remission in MADRS Over Time to the End of the OL Treatment Phase
Zeitfenster: Up to 12 Weeks
|
Percentage of participants in remission (MADRS <= 10 and MADRS <= 12) over time to the end of the OL treatment phase will be reported. The MADRS is a clinician-rated scale designed to measure depression severity and detects changes due to antidepressant treatment. The scale consists of 10 items, each of which is scored from 0 (item not present or normal) to 6 (severe or continuous presence of the symptoms), for a total possible score of 60. Higher scores represent a more severe condition. |
Up to 12 Weeks
|
|
OL Treatment Phase: Change From Baseline in CGI-S Over Time to the End of the OL Treatment Phase
Zeitfenster: Baseline (Day 28) up to 12 Weeks
|
Change from baseline in CGI-S over time to the end of the OL treatment phase will be reported. The CGI-S is a clinician-rated scale that measures illness severity. The CGI has proved to be a robust measure of efficacy in many clinical drug trials and is easy and quick to administer. The CGI-S is rated on a 7-point scale, with the severity of illness scale using a range of responses from 1 (normal) through to 7 (among the most severely ill participants). |
Baseline (Day 28) up to 12 Weeks
|
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OL Treatment Phase: Change From Baseline in MADRS Total Score Over Time to the End of the OL Treatment Phase
Zeitfenster: Baseline (Day 28) up to 12 Weeks
|
Change from baseline in MADRS total score over time to the end of the OL treatment phase will be reported. The MADRS is a clinician-rated scale designed to measure depression severity and detects changes due to antidepressant treatment. The scale consists of 10 items, each of which is scored from 0 (item not present or normal) to 6 (severe or continuous presence of the symptoms), for a total possible score of 60. Higher scores represent a more severe condition. |
Baseline (Day 28) up to 12 Weeks
|
|
OL Treatment Phase: Change From Baseline in Individual MADRS Item Scores Over Time to the End of the OL Treatment Phase
Zeitfenster: Baseline (Day 28) up to 12 Weeks
|
Change from baseline in individual MADRS item scores over time to the end of the OL treatment phase will be reported. The MADRS is a clinician-rated scale designed to measure depression severity and detects changes due to antidepressant treatment. The scale consists of 10 items, each of which is scored from 0 (item not present or normal) to 6 (severe or continuous presence of the symptoms), for a total possible score of 60. Higher scores represent a more severe condition. |
Baseline (Day 28) up to 12 Weeks
|
|
OL Treatment Phase: Change From Baseline in Anhedonia Symptoms Over Time to the End of the OL Treatment Phase As Assessed by MADRS Anhedonia Factor Score
Zeitfenster: Baseline (Day 28) up to 12 Weeks
|
Change from baseline in anhedonia symptoms over time to the end of the OL treatment phase as assessed by MADRS anhedonia factor score will be reported. The MADRS is a clinician-rated scale designed to measure depression severity and detects changes due to antidepressant treatment. The scale consists of 10 items, each of which is scored from 0 (item not present or normal) to 6 (severe or continuous presence of the symptoms), for a total possible score of 60. Higher scores represent a more severe condition. |
Baseline (Day 28) up to 12 Weeks
|
|
OL Treatment Phase: Change From Baseline in Patient-Reported Anhedonia Symptoms Over Time to the End of the OL Treatment Phase As Assessed by PHQ-9 Item 1 Score
Zeitfenster: Baseline (Day 28) up to 12 Weeks
|
Change from baseline in patient-reported anhedonia symptoms over time to the end of the OL treatment phase as assessed by PHQ-9 item 1 score will be reported. The PHQ-9 is a participant-reported outcome measure that will be used to assess depressive symptoms. The scale scores each of the 9 symptom domains of the DSM-5 MDD criteria and it has been used both as a screening tool and a measure of response to treatment for depression. Each item is rated on a 4-point scale (0=not at all, 1=several days, 2=more than half the days, and 3=nearly every day). The participant's item responses are summed to provide a total score (range of 0 to 27) with higher scores indicating greater severity of depressive symptoms. |
Baseline (Day 28) up to 12 Weeks
|
|
OL Treatment Phase: Change From Baseline in PHQ-9 Total Score Over Time to the End of the OL Treatment Phase
Zeitfenster: Baseline (Day 28) up to 12 Weeks
|
Change from baseline in PHQ-9 total score over time to the end of the OL treatment phase will be reported. The PHQ-9 is a participant-reported outcome measure that will be used to assess depressive symptoms. The scale scores each of the 9 symptom domains of the DSM-5 MDD criteria and it has been used both as a screening tool and a measure of response to treatment for depression. Each item is rated on a 4-point scale (0=not at all, 1=several days, 2=more than half the days, and 3=nearly every day). The participant's item responses are summed to provide a total score (range of 0 to 27) with higher scores indicating greater severity of depressive symptoms. |
Baseline (Day 28) up to 12 Weeks
|
|
OL Treatment Phase: Percentage of Responders in PHQ-9 Over Time to the End of the OL Treatment Phase
Zeitfenster: Up to 12 Weeks
|
Percentage of responders (>= 50% reduction from baseline in PHQ-9 total score) over time to the end of the OL treatment phase will be reported. The PHQ-9 is a participant-reported outcome measure that will be used to assess depressive symptoms. The scale scores each of the 9 symptom domains of the DSM-5 MDD criteria and it has been used both as a screening tool and a measure of response to treatment for depression. Each item is rated on a 4-point scale (0=not at all, 1=several days, 2=more than half the days, and 3=nearly every day). The participant's item responses are summed to provide a total score (range of 0 to 27) with higher scores indicating greater severity of depressive symptoms. |
Up to 12 Weeks
|
|
OL Treatment Phase: Percentage of Participants in Remission in PHQ-9 Over Time to the End of the OL Treatment Phase
Zeitfenster: Up to 12 Weeks
|
Percentage of participants in remission (PHQ-9 total score < 5) over time to the end of the OL treatment phase will be reported. The PHQ-9 is a participant-reported outcome measure that will be used to assess depressive symptoms. The scale scores each of the 9 symptom domains of the DSM-5 MDD criteria and it has been used both as a screening tool and a measure of response to treatment for depression. Each item is rated on a 4-point scale (0=not at all, 1=several days, 2=more than half the days, and 3=nearly every day). The participant's item responses are summed to provide a total score (range of 0 to 27) with higher scores indicating greater severity of depressive symptoms. |
Up to 12 Weeks
|
Andere Ergebnismessungen
Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
DB Treatment Phase: Number of Participants with Abnormalities in Blood Oxygen Saturation (SpO2)
Zeitfenster: Up to end of the 4-Week DB treatment phase (Day 28)
|
Number of participants who experience abnormally low blood oxygen saturation will be reported. |
Up to end of the 4-Week DB treatment phase (Day 28)
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DB Treatment Phase: Number of Participants With Treatment-Emergent Adverse Events (TEAEs)
Zeitfenster: Up to end of the 4-Week DB treatment phase (Day 28)
|
An AE is any untoward medical occurrence in a clinical study participant administered a pharmaceutical (investigational or non-investigational) product. An AE does not necessarily have a causal relationship with the intervention. An AE can therefore be any unfavorable and unintended sign (including an abnormal finding), symptom, or disease temporally associated with the use of a medicinal (investigational or non-investigational) product, whether or not related to that medicinal (investigational or non-investigational) product. TEAEs are defined as any adverse event occurring at or after the administration of study intervention. |
Up to end of the 4-Week DB treatment phase (Day 28)
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DB Treatment Phase: Suicidal Ideation and Behavior as Assessed Using the Columbia Suicide Severity Rating Scale (C-SSRS)
Zeitfenster: Up to end of the 4-Week DB treatment phase (Day 28)
|
The C-SSRS is a clinical interview providing a summary of both ideation and behavior that can be administered during any evaluation or risk assessment to identify the level and type of suicidality present. The C-SSRS can also be used during treatment to monitor for clinical worsening. |
Up to end of the 4-Week DB treatment phase (Day 28)
|
|
DB Treatment Phase: Number of Participants with Effects on Dissociative Symptoms As Measured Using the Clinician Administered Dissociative States Scale (CADSS)
Zeitfenster: Up to end of the 4-Week DB treatment phase (Day 28)
|
The CADSS will be administered to assess treatment-emergent dissociative symptoms. It comprises 23 subjective items, divided into 3 components: depersonalization (items 3-7, 20, 23), derealization (items 1-2, 8-13, 16-19, 21) and amnesia (items 14-15, 22). Participant's responses are coded on a 5-point scale (0 = "Not at all" through to 4 = "Extremely"). A higher score indicates a more severe condition. |
Up to end of the 4-Week DB treatment phase (Day 28)
|
|
DB Treatment Phase: Number of Participants with Abnormalities in Physical Examination
Zeitfenster: Up to end of the 4-Week DB treatment phase (Day 28)
|
Number of participants with abnormalities in physical examination will be reported. |
Up to end of the 4-Week DB treatment phase (Day 28)
|
|
DB Treatment Phase: Number of Participants with Abnormalities in Vital Signs
Zeitfenster: Up to end of the 4-Week DB treatment phase (Day 28)
|
Number of participants with abnormalities in vital signs (blood pressure, pulse/heart rate measurements, and temperature) will be reported. |
Up to end of the 4-Week DB treatment phase (Day 28)
|
|
DB Treatment Phase: Number of Participants Reporting Clinically Meaningful Changes in Body Weight
Zeitfenster: Up to end of the 4-Week DB treatment phase (Day 28)
|
Number of participants reporting clinically meaningful changes in body weight will be reported. |
Up to end of the 4-Week DB treatment phase (Day 28)
|
|
DB Treatment Phase: Number of Participants with Abnormalities in 12-lead Electrocardiogram (ECG)
Zeitfenster: Up to end of the 4-Week DB treatment phase (Day 28)
|
Number of participants with abnormalities in 12-lead ECG will be reported. |
Up to end of the 4-Week DB treatment phase (Day 28)
|
|
OL Treatment Phase: Number of Participants with Abnormalities in SpO2
Zeitfenster: Up to 12 Weeks
|
Number of participants who experience abnormally low blood oxygen saturation will be reported. |
Up to 12 Weeks
|
|
OL Treatment Phase: Number of Participants With TEAEs
Zeitfenster: Up to 12 Weeks
|
An AE is any untoward medical occurrence in a clinical study participant administered a pharmaceutical (investigational or non-investigational) product. An AE does not necessarily have a causal relationship with the intervention. An AE can therefore be any unfavorable and unintended sign (including an abnormal finding), symptom, or disease temporally associated with the use of a medicinal (investigational or non-investigational) product, whether or not related to that medicinal (investigational or non-investigational) product. TEAEs are defined as any adverse event occurring at or after the administration of study intervention. |
Up to 12 Weeks
|
|
OL Treatment Phase: Suicidal Ideation and Behavior as Assessed Using the C-SSRS
Zeitfenster: Up to 12 Weeks
|
The C-SSRS is a clinical interview providing a summary of both ideation and behavior that can be administered during any evaluation or risk assessment to identify the level and type of suicidality present. The C-SSRS can also be used during treatment to monitor for clinical worsening. |
Up to 12 Weeks
|
|
OL Treatment Phase: Number of Participants with Abnormalities in Vital Signs
Zeitfenster: Up to 12 Weeks
|
Number of participants with abnormalities in vital signs (blood pressure, pulse/heart rate measurements, and temperature) will be reported. |
Up to 12 Weeks
|
|
OL Treatment Phase: Number of Participants Reporting Clinically Meaningful Changes in Body Weight
Zeitfenster: Up to 12 Weeks
|
Number of participants reporting clinically meaningful changes in body weight will be reported. |
Up to 12 Weeks
|
|
OL Treatment Phase: Number of Participants with Abnormalities in 12-lead ECG
Zeitfenster: Up to 12 Weeks
|
Number of participants with abnormalities in 12-lead ECG will be reported. |
Up to 12 Weeks
|
|
OL Treatment Phase: Number of Participants with Potential Withdrawal Symptoms After Stopping Study Drug Treatment as Measured by the Physician Withdrawal Checklist (PWC-20)
Zeitfenster: Up to 12 Weeks
|
The PWC-20 is a 20-item simple and accurate method to assess potential development of discontinuation symptoms after stopping of study medication. The PWC-20 is a reliable and sensitive instrument for the assessment of discontinuation symptoms. |
Up to 12 Weeks
|
Mitarbeiter und Ermittler
Sponsor
Sponsor
Ermittler
Ermittler
- Studienleiter: Janssen Research & Development, LLC Clinical Trial, Janssen Research & Development, LLC
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Studienbeginn
Primärer Abschluss (Geschätzt)
Primärer Abschluss
Studienabschluss (Geschätzt)
Studienabschluss
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Zuerst gepostet
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes Update gepostet
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
Andere Studien-ID-Nummern
- 54135419TRD3015
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Beschreibung des IPD-Plans
The data sharing policy of Johnson & Johnson Innovative Medicine is available at innovativemedicine.jnj.com/our-innovation/clinical-trials/transparency. As noted on this site, requests for access to the study data can be submitted through Yale Open Data Access (YODA) Project site at yoda.yale.edu
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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