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A Study of CLE-100 (Oral Esketamine) in Addition to Standard Antidepressant Drug for Major Depressive Disorder - CLEO Study

Primary Purpose

Adjunctive Treatment of Major Depressive Disorder

Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
CLE-100
placebo
Sponsored by
Clexio Biosciences Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Adjunctive Treatment of Major Depressive Disorder focused on measuring MDD, depression, depressive disorder, major depression, adjunct therapy, oral, esketamine

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Part A - Inclusion Criteria:

  1. Male or female between 18 to 60 years of age
  2. Primary diagnosis of MDD, without psychotic features according to DSM-5 and supported by the Mini International Neuropsychiatric Interview (MINI)
  3. MADRS score of at least 18 at Screening
  4. Treatment with stable dose of the current antidepressant therapy for at least 4 weeks for the current major depressive episode (MDE)
  5. Body mass index (BMI) between 18 and 40 kg/m2, inclusive
  6. Is able and competent to read and sign the informed consent form (ICF).

Part A - Exclusion Criteria:

  1. History of substance use disorder per DSM-5 criteria, except for tobacco use disorder
  2. History or current diagnosis of bipolar disorder, schizophrenia, schizoaffective disorders, binge eating disorder dementia, delirium, amnesia, or any other significant cognitive disorder
  3. Posttraumatic stress disorder, obsessive compulsive disorder, or any other mental disorder (including personality disorders)
  4. Has any medical condition for which an increase in blood pressure or intracranial pressure poses a serious risk
  5. Female of childbearing potential without appropriate contraceptive means, pregnant or breastfeeding

Part B - Inclusion Criteria:

  1. Male or female between 18 to 65 years of age
  2. Primary diagnosis of MDD without psychotic features according to DSM-5 and supported by the Mini International Neuropsychiatric Interview (MINI)
  3. MADRS score of at least 24 at Screening.
  4. At least 2 inadequate responses to antidepressant therapy (ADT) in the current Major Depressive Episode (MDE)
  5. Current MDE for at least 12 weeks
  6. BMI between 18 and 40 kg/m2, inclusive.
  7. Is able and competent to read and sign the ICF.

Part B - Exclusion Criteria:

  1. Inadequate response to more than 5 treatment courses of antidepressant medication therapy during the current MDE
  2. Current MDE for longer than 5 years.
  3. 3. Has a current substance use disorder or history of any substance use disorder per DSM-5 criteria within 12 months prior to Screening, except for tobacco use disorder.
  4. Has a history or current diagnosis of bipolar disorder, schizophrenia, or schizoaffective disorders.
  5. Has dementia, delirium, amnesia, or any other significant cognitive disorder.
  6. Has posttraumatic stress disorder, obsessive compulsive disorder, or any other mental disorder (including personality disorders, eating disorders, etc.).
  7. Has any medical condition for which an increase in blood pressure or intracranial pressure poses a serious risk.
  8. Has been randomized in Part A of this study.
  9. Is a female of childbearing potential pregnant or breastfeeding.

Sites / Locations

  • Clinical Site 126
  • Clinical Site 120
  • Clinical Site 129
  • Clinical Site 141
  • Clinical Site 115
  • Clinical Site 132
  • Clinical Site 117
  • Clinical Site 113
  • Clinical Site 123
  • Clinical Site 124
  • Clinical Site 142
  • Clinical Site 112
  • Clinical Site 145
  • Clinical Site 107
  • Clinical Site 108
  • Clinical Site 116
  • Clinical Site 105
  • Clinical Site 137
  • Clinical Site 140
  • Clinical Site 104
  • Clinical Site 122
  • Clinical Site 131
  • Clinical Site 136
  • Clinical Site 103
  • Clinical Site 121
  • Clinical Site 151
  • Clinical Site 139
  • Clinical Site 125
  • Clinical Site 110
  • Clinical Site 101
  • Clinical Site 148
  • Clinical Site 128
  • Clinical Site 102
  • Clinical Site 111
  • Clinical Site 143
  • Clinical Site 138
  • Clinical Site 127
  • Clinical Site 106
  • Clinical Site 118
  • Clinical Site 114
  • Clinical Site 109
  • Clinical Site 149
  • Clinical Site 144
  • Clinical Site 147
  • Clinical Site 135
  • Clinical Site 150

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Placebo Comparator

Experimental

Placebo Comparator

Arm Label

Part A - CLE-100 (oral esketamine)

Part A - Placebo

Part B - CLE-100 (oral esketamine)

Part B - Placebo

Arm Description

Part A: 1 oral tablet of CLE-100 once daily for 1 week.

Part A: 1 oral tablet of Placebo once daily for 1 week.

Part B: 1 oral tablet of CLE-100 once daily for 4 weeks.

Part B: 1 oral tablet of Placebo once daily for 4 weeks.

Outcomes

Primary Outcome Measures

Part A - Frequency of adverse events
Part A - Self-Administered Karolinska Sleepiness Scale
The Karolinska Sleepiness Scale is a single-item, subjective, self-reported instrument measuring sleepiness on a 9-point Likert scale (1 to 9), where a higher value represents a worse outcome.
Part A - Modified Observer's Assessment of Alertness/Sedation Scale (MOAA/S)
The MOAA/S will be used to measure treatment-emergent sedation. The MOAA/S is a widely used clinician-administered measure of alertness/sedation for clinical trials. The MOAA/S measures the alertness/sedation spectrum on a 6-point scale (0 to 5) based on verbal cues, where a higher value represents a better outcome.
Part A - Clinician-Administered Dissociative Symptoms Scale (CADSS)
The CADSS will be administered to assess treatment-emergent dissociative symptoms. The CADSS is a 23-item instrument that is clinician-administered. Each item is scored on a 5-point scale (0 to 4. A higher value represents a worse outcome. The CADSS total score ranges between 0 and 92.
Part A - Columbia Suicide Severity Rating Scale (C-SSRS)
The C-SSRS will be performed to assess suicidal ideation and behavior. The C-SSRS is an instrument used to assess suicide risk by measuring symptoms of suicidal ideation, self-harm, and suicidal behavior that is administered by trained personnel. The suicidal ideation is evaluated with a "yes/no" questionnaire and the suicidal behavior severity is scored on a 6-point scale (0 to 5) where a higher value represents a more severe behavior.
Part A - Four-items positive subscale from the Brief Psychiatric Rating Scale (BPRS)
Four items of the BPRS will be administered to assess treatment-emergent psychotic symptoms. The BPRS is a widely used, clinician-administered instrument that involves 4 subscales: Negative Symptoms, Positive Symptoms, Manic-Hostility, and Anxiety/Depression. The 4-item Positive Symptoms subscale of the BPRS will be used to screen for potential psychiatric symptoms (suspiciousness, hallucinations, unusual thought content, and conceptual disorganization). Each item is scored on a 7-point scale (1 to 7). where a higher value represents a worse outcome. The 4 items BPRS total score ranges between 4 and 28.
Part A - 20-item Physician Withdrawal Checklist (PWC-20)
The PWC-20 is a clinician-administered assessment to evaluate potential withdrawal symptoms following cessation of the double-blind treatment. The PWC-20 is a shortened version of the original 35-item instrument used to determine withdraw symptoms in subjects following discontinuation of anxiolytics. The items are evaluated on a 4-point scale (0 to 3) where a higher value represents a worse outcome. The total score ranges between 0 to 60.
Part A - Cognitive function evaluated by Cogstate battery
The Cogstate battery of cognitive tests will be used to measure psychomotor function, attention, visual learning, and working memory. The Cogstate battery will include the following tests: Detection Test, Identification Test, One Back Test, Groton Maze Test.
Part A - Digit Symbol Substitution Test (DSST)
The DSST is a psychometric test assessing the integrity of executive function, processing speed, attention, spatial perception, and visual scanning, which are functions required for driving, and will be performed repeatedly. The DSST is a valid and sensitive instrument to evaluate cognitive dysfunction and changes in cognitive function. The DSST is a timed test taken by the subject and scored based on both the number of correct answers and the speed at which they were determined. The score ranges between 0 to 135.
Part A - Pharmacokinetics of CLE-100 (Cmax)
Maximum observed plasma concentration (Cmax)
Part A - Pharmacokinetics of CLE-100 (Tmax)
Time of maximum observed plasma concentration (Tmax)
Part A - Pharmacokinetics of CLE-100 (AUC)
Area under the concentration curve
Part B - Change from baseline in Montgomery-Asberg Depression Rating Scale (MADRS) score
The MADRS is a validated clinician-administered measurement of depression severity commonly used in clinical trials of depression treatments to select subjects and assess efficacy. The test 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.

Secondary Outcome Measures

Part B - Change from baseline in Symptoms of Depression Questionnaire (SDQ) score
The SDQ is a 44-item self-report scale for the assessment of MDD that includes assessments for irritability, anger attacks, and anxiety symptoms. Higher scores represent a more severe condition.
Part B - Change from baseline in Sheehan Disability Scale (SDS)
The SDS is a 3-item, self-completion instrument to assess functional impairments associated with work/school, social life and leisure activities, and family life and home responsibilities utilizing a 10-point scale.
Part B - Change from baseline in Montgomery-Asberg Depression Rating Scale (MADRS) score
The MADRS is a validated clinician-administered measurement of depression severity commonly used in clinical trials of depression treatments to select subjects and assess efficacy. The test 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.
Part B - Change from baseline in Clinical Global Impression - Severity (CGI-S) score
The CGI-S is a well-known and frequently used clinician-administered instrument for the assessment of MDD that weighs the clinical impact of the identified symptom(s) on behavior and function. The CGI-S grades measures of psychopathology on a scale from 1 to 7.

Full Information

First Posted
September 9, 2019
Last Updated
September 10, 2023
Sponsor
Clexio Biosciences Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT04103892
Brief Title
A Study of CLE-100 (Oral Esketamine) in Addition to Standard Antidepressant Drug for Major Depressive Disorder - CLEO Study
Official Title
A Two-Part Study of CLE-100 as an Adjunct Therapy in Subjects With Major Depressive Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
September 5, 2019 (Actual)
Primary Completion Date
September 21, 2022 (Actual)
Study Completion Date
October 5, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Clexio Biosciences Ltd.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The clinical trial is a Phase 2, double-blind, randomized, placebo controlled study in Major Depressive Disorder (MDD) participants currently treated with antidepressant therapy. The objective of the study is to assess CLE-100 for the treatment of MDD in participants currently treated with standard antidepressant therapy.
Detailed Description
CLEO study is performed in two parts (part A and Part B). The sponsor is currently recruiting only for the Part B of the study. Part A will be an inpatient study to assess the safety, tolerability, and pharmacokinetics of CLE-100 (oral esketamine) in MDD participants currently treated with an antidepressant drug. It will include a screening phase (up to 35 days), a 1 week inpatient double-blind treatment phase and an outpatient post treatment safety follow-up phase of 1 week after last study drug administration. Part B will be a study to assess the safety and efficacy of CLE-100 (oral esketamine) in MDD participants currently treated with an antidepressant drug with inadequate response to standard antidepressant therapy. The participants will remain on their current antidepressant therapy with no dose change during the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adjunctive Treatment of Major Depressive Disorder
Keywords
MDD, depression, depressive disorder, major depression, adjunct therapy, oral, esketamine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Part A - 15 patients, 2 arms, parallel; Part B - 122 patients, 2 arms, parallel
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
130 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Part A - CLE-100 (oral esketamine)
Arm Type
Experimental
Arm Description
Part A: 1 oral tablet of CLE-100 once daily for 1 week.
Arm Title
Part A - Placebo
Arm Type
Placebo Comparator
Arm Description
Part A: 1 oral tablet of Placebo once daily for 1 week.
Arm Title
Part B - CLE-100 (oral esketamine)
Arm Type
Experimental
Arm Description
Part B: 1 oral tablet of CLE-100 once daily for 4 weeks.
Arm Title
Part B - Placebo
Arm Type
Placebo Comparator
Arm Description
Part B: 1 oral tablet of Placebo once daily for 4 weeks.
Intervention Type
Drug
Intervention Name(s)
CLE-100
Intervention Description
1 tablet of CLE-100 administered once daily
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
1 tablet of placebo administered once daily
Primary Outcome Measure Information:
Title
Part A - Frequency of adverse events
Time Frame
14 days
Title
Part A - Self-Administered Karolinska Sleepiness Scale
Description
The Karolinska Sleepiness Scale is a single-item, subjective, self-reported instrument measuring sleepiness on a 9-point Likert scale (1 to 9), where a higher value represents a worse outcome.
Time Frame
7 days
Title
Part A - Modified Observer's Assessment of Alertness/Sedation Scale (MOAA/S)
Description
The MOAA/S will be used to measure treatment-emergent sedation. The MOAA/S is a widely used clinician-administered measure of alertness/sedation for clinical trials. The MOAA/S measures the alertness/sedation spectrum on a 6-point scale (0 to 5) based on verbal cues, where a higher value represents a better outcome.
Time Frame
7 days
Title
Part A - Clinician-Administered Dissociative Symptoms Scale (CADSS)
Description
The CADSS will be administered to assess treatment-emergent dissociative symptoms. The CADSS is a 23-item instrument that is clinician-administered. Each item is scored on a 5-point scale (0 to 4. A higher value represents a worse outcome. The CADSS total score ranges between 0 and 92.
Time Frame
7 days
Title
Part A - Columbia Suicide Severity Rating Scale (C-SSRS)
Description
The C-SSRS will be performed to assess suicidal ideation and behavior. The C-SSRS is an instrument used to assess suicide risk by measuring symptoms of suicidal ideation, self-harm, and suicidal behavior that is administered by trained personnel. The suicidal ideation is evaluated with a "yes/no" questionnaire and the suicidal behavior severity is scored on a 6-point scale (0 to 5) where a higher value represents a more severe behavior.
Time Frame
7 days
Title
Part A - Four-items positive subscale from the Brief Psychiatric Rating Scale (BPRS)
Description
Four items of the BPRS will be administered to assess treatment-emergent psychotic symptoms. The BPRS is a widely used, clinician-administered instrument that involves 4 subscales: Negative Symptoms, Positive Symptoms, Manic-Hostility, and Anxiety/Depression. The 4-item Positive Symptoms subscale of the BPRS will be used to screen for potential psychiatric symptoms (suspiciousness, hallucinations, unusual thought content, and conceptual disorganization). Each item is scored on a 7-point scale (1 to 7). where a higher value represents a worse outcome. The 4 items BPRS total score ranges between 4 and 28.
Time Frame
7 days
Title
Part A - 20-item Physician Withdrawal Checklist (PWC-20)
Description
The PWC-20 is a clinician-administered assessment to evaluate potential withdrawal symptoms following cessation of the double-blind treatment. The PWC-20 is a shortened version of the original 35-item instrument used to determine withdraw symptoms in subjects following discontinuation of anxiolytics. The items are evaluated on a 4-point scale (0 to 3) where a higher value represents a worse outcome. The total score ranges between 0 to 60.
Time Frame
14 days
Title
Part A - Cognitive function evaluated by Cogstate battery
Description
The Cogstate battery of cognitive tests will be used to measure psychomotor function, attention, visual learning, and working memory. The Cogstate battery will include the following tests: Detection Test, Identification Test, One Back Test, Groton Maze Test.
Time Frame
7 days
Title
Part A - Digit Symbol Substitution Test (DSST)
Description
The DSST is a psychometric test assessing the integrity of executive function, processing speed, attention, spatial perception, and visual scanning, which are functions required for driving, and will be performed repeatedly. The DSST is a valid and sensitive instrument to evaluate cognitive dysfunction and changes in cognitive function. The DSST is a timed test taken by the subject and scored based on both the number of correct answers and the speed at which they were determined. The score ranges between 0 to 135.
Time Frame
7 days
Title
Part A - Pharmacokinetics of CLE-100 (Cmax)
Description
Maximum observed plasma concentration (Cmax)
Time Frame
7 days
Title
Part A - Pharmacokinetics of CLE-100 (Tmax)
Description
Time of maximum observed plasma concentration (Tmax)
Time Frame
7 days
Title
Part A - Pharmacokinetics of CLE-100 (AUC)
Description
Area under the concentration curve
Time Frame
8 days
Title
Part B - Change from baseline in Montgomery-Asberg Depression Rating Scale (MADRS) score
Description
The MADRS is a validated clinician-administered measurement of depression severity commonly used in clinical trials of depression treatments to select subjects and assess efficacy. The test 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.
Time Frame
29 days
Secondary Outcome Measure Information:
Title
Part B - Change from baseline in Symptoms of Depression Questionnaire (SDQ) score
Description
The SDQ is a 44-item self-report scale for the assessment of MDD that includes assessments for irritability, anger attacks, and anxiety symptoms. Higher scores represent a more severe condition.
Time Frame
29 days
Title
Part B - Change from baseline in Sheehan Disability Scale (SDS)
Description
The SDS is a 3-item, self-completion instrument to assess functional impairments associated with work/school, social life and leisure activities, and family life and home responsibilities utilizing a 10-point scale.
Time Frame
29 days
Title
Part B - Change from baseline in Montgomery-Asberg Depression Rating Scale (MADRS) score
Description
The MADRS is a validated clinician-administered measurement of depression severity commonly used in clinical trials of depression treatments to select subjects and assess efficacy. The test 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.
Time Frame
15 days
Title
Part B - Change from baseline in Clinical Global Impression - Severity (CGI-S) score
Description
The CGI-S is a well-known and frequently used clinician-administered instrument for the assessment of MDD that weighs the clinical impact of the identified symptom(s) on behavior and function. The CGI-S grades measures of psychopathology on a scale from 1 to 7.
Time Frame
29 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Part A - Inclusion Criteria: Male or female between 18 to 60 years of age Primary diagnosis of MDD, without psychotic features according to DSM-5 and supported by the Mini International Neuropsychiatric Interview (MINI) MADRS score of at least 18 at Screening Treatment with stable dose of the current antidepressant therapy for at least 4 weeks for the current major depressive episode (MDE) Body mass index (BMI) between 18 and 40 kg/m2, inclusive Is able and competent to read and sign the informed consent form (ICF). Part A - Exclusion Criteria: History of substance use disorder per DSM-5 criteria, except for tobacco use disorder History or current diagnosis of bipolar disorder, schizophrenia, schizoaffective disorders, binge eating disorder dementia, delirium, amnesia, or any other significant cognitive disorder Posttraumatic stress disorder, obsessive compulsive disorder, or any other mental disorder (including personality disorders) Has any medical condition for which an increase in blood pressure or intracranial pressure poses a serious risk Female of childbearing potential without appropriate contraceptive means, pregnant or breastfeeding Part B - Inclusion Criteria: Male or female between 18 to 65 years of age Primary diagnosis of MDD without psychotic features according to DSM-5 and supported by the Mini International Neuropsychiatric Interview (MINI) MADRS score of at least 24 at Screening. At least 2 inadequate responses to antidepressant therapy (ADT) in the current Major Depressive Episode (MDE) Current MDE for at least 12 weeks BMI between 18 and 40 kg/m2, inclusive. Is able and competent to read and sign the ICF. Part B - Exclusion Criteria: Inadequate response to more than 5 treatment courses of antidepressant medication therapy during the current MDE Current MDE for longer than 5 years. 3. Has a current substance use disorder or history of any substance use disorder per DSM-5 criteria within 12 months prior to Screening, except for tobacco use disorder. Has a history or current diagnosis of bipolar disorder, schizophrenia, or schizoaffective disorders. Has dementia, delirium, amnesia, or any other significant cognitive disorder. Has posttraumatic stress disorder, obsessive compulsive disorder, or any other mental disorder (including personality disorders, eating disorders, etc.). Has any medical condition for which an increase in blood pressure or intracranial pressure poses a serious risk. Has been randomized in Part A of this study. Is a female of childbearing potential pregnant or breastfeeding.
Facility Information:
Facility Name
Clinical Site 126
City
Bentonville
State/Province
Arkansas
ZIP/Postal Code
72712
Country
United States
Facility Name
Clinical Site 120
City
Little Rock
State/Province
Arkansas
ZIP/Postal Code
72209
Country
United States
Facility Name
Clinical Site 129
City
Little Rock
State/Province
Arkansas
ZIP/Postal Code
72209
Country
United States
Facility Name
Clinical Site 141
City
Anaheim
State/Province
California
ZIP/Postal Code
92805
Country
United States
Facility Name
Clinical Site 115
City
Bellflower
State/Province
California
ZIP/Postal Code
90706
Country
United States
Facility Name
Clinical Site 132
City
Lafayette
State/Province
California
ZIP/Postal Code
94549
Country
United States
Facility Name
Clinical Site 117
City
Oakland
State/Province
California
ZIP/Postal Code
94607
Country
United States
Facility Name
Clinical Site 113
City
Oceanside
State/Province
California
ZIP/Postal Code
92056
Country
United States
Facility Name
Clinical Site 123
City
Riverside
State/Province
California
ZIP/Postal Code
92506
Country
United States
Facility Name
Clinical Site 124
City
Santa Ana
State/Province
California
ZIP/Postal Code
92705
Country
United States
Facility Name
Clinical Site 142
City
Santa Rosa
State/Province
California
ZIP/Postal Code
95401
Country
United States
Facility Name
Clinical Site 112
City
Torrance
State/Province
California
ZIP/Postal Code
90502
Country
United States
Facility Name
Clinical Site 145
City
Denver
State/Province
Colorado
ZIP/Postal Code
80209
Country
United States
Facility Name
Clinical Site 107
City
Hialeah
State/Province
Florida
ZIP/Postal Code
33016
Country
United States
Facility Name
Clinical Site 108
City
Miami Gardens
State/Province
Florida
ZIP/Postal Code
33014
Country
United States
Facility Name
Clinical Site 116
City
Miami
State/Province
Florida
ZIP/Postal Code
33145
Country
United States
Facility Name
Clinical Site 105
City
Orlando
State/Province
Florida
ZIP/Postal Code
32803
Country
United States
Facility Name
Clinical Site 137
City
Orlando
State/Province
Florida
ZIP/Postal Code
32807
Country
United States
Facility Name
Clinical Site 140
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30338
Country
United States
Facility Name
Clinical Site 104
City
Decatur
State/Province
Georgia
ZIP/Postal Code
30030
Country
United States
Facility Name
Clinical Site 122
City
Marietta
State/Province
Georgia
ZIP/Postal Code
30060
Country
United States
Facility Name
Clinical Site 131
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21208
Country
United States
Facility Name
Clinical Site 136
City
Rockville
State/Province
Maryland
ZIP/Postal Code
20877
Country
United States
Facility Name
Clinical Site 103
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States
Facility Name
Clinical Site 121
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02131
Country
United States
Facility Name
Clinical Site 151
City
Dearborn Heights
State/Province
Michigan
ZIP/Postal Code
48034
Country
United States
Facility Name
Clinical Site 139
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63128
Country
United States
Facility Name
Clinical Site 125
City
Lincoln
State/Province
Nebraska
ZIP/Postal Code
68526
Country
United States
Facility Name
Clinical Site 110
City
Las Vegas
State/Province
Nevada
ZIP/Postal Code
89102
Country
United States
Facility Name
Clinical Site 101
City
Marlton
State/Province
New Jersey
ZIP/Postal Code
08053
Country
United States
Facility Name
Clinical Site 148
City
Toms River
State/Province
New Jersey
ZIP/Postal Code
08755
Country
United States
Facility Name
Clinical Site 128
City
New York
State/Province
New York
ZIP/Postal Code
10036
Country
United States
Facility Name
Clinical Site 102
City
Staten Island
State/Province
New York
ZIP/Postal Code
10312
Country
United States
Facility Name
Clinical Site 111
City
Hickory
State/Province
North Carolina
ZIP/Postal Code
28601
Country
United States
Facility Name
Clinical Site 143
City
Raleigh
State/Province
North Carolina
ZIP/Postal Code
27609
Country
United States
Facility Name
Clinical Site 138
City
Middleburg Heights
State/Province
Ohio
ZIP/Postal Code
44130
Country
United States
Facility Name
Clinical Site 127
City
North Canton
State/Province
Ohio
ZIP/Postal Code
44720
Country
United States
Facility Name
Clinical Site 106
City
Media
State/Province
Pennsylvania
ZIP/Postal Code
19063
Country
United States
Facility Name
Clinical Site 118
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
Clinical Site 114
City
Fort Worth
State/Province
Texas
ZIP/Postal Code
76104
Country
United States
Facility Name
Clinical Site 109
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
Clinical Site 149
City
Missouri City
State/Province
Texas
ZIP/Postal Code
88459
Country
United States
Facility Name
Clinical Site 144
City
Plano
State/Province
Texas
ZIP/Postal Code
75093
Country
United States
Facility Name
Clinical Site 147
City
Draper
State/Province
Utah
ZIP/Postal Code
84020
Country
United States
Facility Name
Clinical Site 135
City
Bellevue
State/Province
Washington
ZIP/Postal Code
98007
Country
United States
Facility Name
Clinical Site 150
City
San Juan
ZIP/Postal Code
00918
Country
Puerto Rico

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

A Study of CLE-100 (Oral Esketamine) in Addition to Standard Antidepressant Drug for Major Depressive Disorder - CLEO Study

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