Phase
Condition
Depression
Treatment
Placebo
CLE-100
Clinical Study ID
Ages 18-65 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Male or female between 18 to 65 years of age at Screening
Diagnosis of MDD, single or recurrent, without psychotic features, in the current orprevious episode(s), according to the Diagnostic and Statistical Manual of MentalDisorders-5 (DSM-5). The diagnosis of MDD must be supported by the MiniInternational Neuropsychiatric Interview (MINI) Screen 7.0.2 for DSM-5.
Currently experiencing a Major Depressive Episode (MDE) that began at least 12 weeksbut no more than 5 years prior to Screening. The current MDE must be confirmed bythe independent SAFER assessor.
MADRS score of 24 or higher at Screening as confirmed by an independent SAFERassessor.
At Screening, a history of inadequate response to at least 2 antidepressantmedications in the current MDE. Inadequate response is defined as less than 50%improvement of depression symptoms following at least 6 weeks of treatment with atherapeutic dose and is assessed by the site using the Massachusetts GeneralHospital Antidepressant Treatment Response Questionnaire (MGH-ATRQ). Inadequateresponse to at least 2 antidepressant medications must be verified by documentedmedical or pharmacy records and confirmed by an independent SAFER assessor.
Able and competent to read and sign the informed consent form (ICF).
Exclusion
Exclusion Criteria:
- At Screening, a history of inadequate response (as defined in inclusion criterion
#5) to more than 5 antidepressant medications in the current MDE using MGH-ATRQ andconfirmed by the independent SAFER assessor.
A high risk of suicide based on any of the following:
Item 10 of MADRS score (suicidal thoughts) is 5 or higher at Screening orBaseline.
Suicide attempt in the previous 6 months.
Significant risk, as judged by the Investigator, based on the psychiatricinterview or information collected with the C SSRS at Screening or Baseline.
Current or lifetime history of substance use disorder with ketamine, phencyclidine (PCP), lysergic acid diethylamide (LSD), or 3.4-methylenedioxymethamphetamine (MDMA)hallucinogen-related use disorders or has any other current substance use disorderor history within 12 months prior to Screening (Substance Use Disorder is diagnosedper DSM-5 criteria and does not include tobacco use disorder).
Use of ketamine, esketamine, PCP, or dextromethorphan recreationally in the past 6months.
History or current diagnosis of bipolar disorder, schizophrenia, or schizoaffectivedisorder or other schizophrenia spectrum disorders.
Dementia, delirium, amnesia, or any other significant cognitive disorder.
Any medical condition for which an increase in blood pressure or intracranialpressure or intraocular pressure or tachycardia poses a serious risk (e.g.,aneurysmal vascular disease, arteriovenous malformation, or history of intracerebralhemorrhage).
Study Design
Study Description
Connect with a study center
Clinical Site 139
La Jolla, California 92037
United StatesSite Not Available
Clinical Site 131
Lafayette, California 94549
United StatesSite Not Available
Clinical Site 130
Upland, California 91786
United StatesSite Not Available
Clinical Site 139
La Jolla 5363943, California 5332921 92037
United StatesSite Not Available
Clinical Site 131
Lafayette 5364226, California 5332921 94549
United StatesSite Not Available
Clinical Site 130
Upland 5404915, California 5332921 91786
United StatesSite Not Available
Clinical Site 102
Hollywood, Florida 33024
United StatesSite Not Available
Clinical Site 105
Lauderhill, Florida 33319
United StatesSite Not Available
Clinical SIte 112
Miami Lakes, Florida 33016
United StatesSite Not Available
Clinical Site 140
Miami Springs, Florida 33166
United StatesSite Not Available
Clinical Site 132
Pensacola, Florida 32502
United StatesSite Not Available
Clinical Site 102
Hollywood 4158928, Florida 4155751 33024
United StatesSite Not Available
Clinical Site 105
Lauderhill 4161625, Florida 4155751 33319
United StatesSite Not Available
Clinical Site 140
Miami Springs 4164223, Florida 4155751 33166
United StatesSite Not Available
Clinical Site 132
Pensacola 4168228, Florida 4155751 32502
United StatesSite Not Available
Clinical Site 118
Atlanta, Georgia 30030
United StatesSite Not Available
Clinical Site 138
Marietta, Georgia 30060
United StatesSite Not Available
Clinical Site 114
Savannah, Georgia 31405
United StatesSite Not Available
Clinical Site 118
Atlanta 4180439, Georgia 4197000 30030
United StatesSite Not Available
Clinical Site 138
Marietta 4207783, Georgia 4197000 30060
United StatesSite Not Available
Clinical Site 114
Savannah 4221552, Georgia 4197000 31405
United StatesSite Not Available
Clinical Site 127
Chicago, Illinois 60640
United StatesSite Not Available
Clinical Site 120
Elgin, Illinois 60123
United StatesSite Not Available
Clinical Site 127
Chicago 4887398, Illinois 4896861 60640
United StatesSite Not Available
Clinical Site 120
Elgin 4890864, Illinois 4896861 60123
United StatesSite Not Available
Clinical Site 108
Gaithersburg, Maryland 20877
United StatesSite Not Available
Clinical Site 108
Gaithersburg 4355843, Maryland 4361885 20877
United StatesSite Not Available
Clinical Site 116
Flowood, Mississippi 39232
United StatesSite Not Available
Clinical Site 116
Flowood 4426822, Mississippi 4436296 39232
United StatesSite Not Available
Clinical Site 126
O'Fallon, Missouri 63368
United StatesSite Not Available
Clinical Site 126
O'Fallon 4401242, Missouri 4398678 63368
United StatesSite Not Available
Clinical Site 128
Marlton, New Jersey 08054
United StatesSite Not Available
Clinical Site 101
Toms River, New Jersey 08755
United StatesSite Not Available
Clinical Site 101
Toms River 4504476, New Jersey 5101760 08755
United StatesSite Not Available
Clinical Site 133
New York, New York 10036
United StatesSite Not Available
Clinical Site 103
Beachwood, Ohio 44236
United StatesSite Not Available
Clinical Site 119
North Canton, Ohio 44720
United StatesSite Not Available
Clinical Site 103
Beachwood 5146711, Ohio 5165418 44236
United StatesSite Not Available
Clinical Site 119
North Canton 5164706, Ohio 5165418 44720
United StatesSite Not Available
Clinical Site 135
Oklahoma City, Oklahoma 73112
United StatesSite Not Available
Clinical Site 135
Oklahoma City 4544349, Oklahoma 4544379 73112
United StatesSite Not Available
Clinical Site 107
Austin, Texas 78737
United StatesSite Not Available
Clinical Site 106
DeSoto, Texas 75115
United StatesSite Not Available
Clinical Site 137
Plano, Texas 75093
United StatesSite Not Available
Clinical Site 107
Austin 4671654, Texas 4736286 78737
United StatesSite Not Available
Clinical Site 137
Plano 4719457, Texas 4736286 75093
United StatesSite Not Available
Clinical Site 117
Murray, Utah 84107
United StatesSite Not Available
Clinical Site 117
Murray 5778755, Utah 5549030 84107
United StatesSite Not Available
Clinical Site 115
Bellevue, Washington 98007
United StatesSite Not Available
Clinical Site 115
Bellevue 5786882, Washington 5815135 98007
United StatesSite Not Available

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