The study is a Phase 2, double-blind, randomized, placebo-controlled study in Major Depressive Disorder (MDD) participants with an inadequate response to standard antidepressants The objective of the study is to assess CLE-100 (oral esketamine) for the treatment of MDD in participants currently treated with an oral antidepressant medication and who have an inadequate response to at least 2 antidepressants.
This is a Phase 2 study in subjects with MDD currently treated with an oral antidepressant medication with an inadequate response to at least 2 antidepressants. SOLEO will be an outpatient study to assess the safety, efficacy, and tolerability of CLE-100 as compared to placebo. Eligible subjects will be randomized to receive either placebo or CLE-100 (oral esketamine) once daily in addition to their current oral antidepressant monotherapy for 4 weeks. All subjects who adequately completed the 4-week Double-Blind Treatment Period and who meet the eligibility criteria will be offered the option to roll-over to a 6-month Open-label Extension (OLE) Treatment Period with CLE-100.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
99
Clinical Site 139
La Jolla, California, United States
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.
Time frame: 29 days
Change From Baseline in the Clinical Global Impression - Severity (CGI-S)
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
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.
Time frame: 2 weeks
Safety Outcomes: Assessment of the Safety and Tolerability of CLE-100 Compared to Placebo
Assessment of the safety and tolerability of CLE-100 compared to placebo using the following assessments: * Adverse Events (AEs) * Adverse events of special interest (AESIs) * Clinical laboratory evaluations * Vital signs * 12-lead electrocardiogram * Modified Observer's Assessment of Alertness/Sedation scale (MOAA/S) * Clinician-Administered Dissociative State Scale (CADSS) * Incidence of suicidal ideation or behavior as assessed by the Columbia-Suicide Severity Rating Scale (C-SSRS) * 4-item Brief Psychiatric Rating Scale (BPRS) * 20-item Physician Withdrawal Checklist (PWC-20) * Bladder Pain/Interstitial Cystitis Symptom Score (BPIC-SS) * Digit Symbol Substitution Test (DSST) * Discontinuation rates and reason(s) for discontinuation
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Clinical Site 131
Lafayette, California, United States
Clinical Site 130
Upland, California, United States
Clinical Site 102
Hollywood, Florida, United States
Clinical Site 105
Lauderhill, Florida, United States
Clinical Site 140
Miami Springs, Florida, United States
Clinical Site 132
Pensacola, Florida, United States
Clinical Site 118
Atlanta, Georgia, United States
Clinical Site 138
Marietta, Georgia, United States
Clinical Site 114
Savannah, Georgia, United States
...and 13 more locations
Time frame: Through study completion, an average of 7 months