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CompletedPhase 2Results posted

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

NCT04103892 · Clexio Biosciences Ltd.

Closed to entry
Status
Not accepting participants
Phase 2
Phase
146
Target enrolment
46
Study sites
19 US states

What it is testing

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.

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • Part B - Change From Baseline in Montgomery-Asberg Depression Rating Scale (MADRS) Score

    Measured over 29 days

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

18 Years to 65 Years
Ages
All
Sex
Not accepted
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.

Where

46 study sites

FacilityCityRegionCountry
Clinical Site 126BentonvilleArkansasUnited States
Clinical Site 120Little RockArkansasUnited States
Clinical Site 129Little RockArkansasUnited States
Clinical Site 141AnaheimCaliforniaUnited States
Clinical Site 115BellflowerCaliforniaUnited States
Clinical Site 132LafayetteCaliforniaUnited States
Clinical Site 117OaklandCaliforniaUnited States
Clinical Site 113OceansideCaliforniaUnited States
Clinical Site 123RiversideCaliforniaUnited States
Clinical Site 124Santa AnaCaliforniaUnited States
Clinical Site 142Santa RosaCaliforniaUnited States
Clinical Site 112TorranceCaliforniaUnited States
Clinical Site 145DenverColoradoUnited States
Clinical Site 107HialeahFloridaUnited States
Clinical Site 116MiamiFloridaUnited States
Clinical Site 108Miami GardensFloridaUnited States
Clinical Site 105OrlandoFloridaUnited States
Clinical Site 137OrlandoFloridaUnited States
Clinical Site 140AtlantaGeorgiaUnited States
Clinical Site 104DecaturGeorgiaUnited States
Clinical Site 122MariettaGeorgiaUnited States
Clinical Site 131BaltimoreMarylandUnited States
Clinical Site 136RockvilleMarylandUnited States
Clinical Site 103BostonMassachusettsUnited States
Clinical Site 121BostonMassachusettsUnited States
Clinical Site 151Dearborn HeightsMichiganUnited States
Clinical Site 139St LouisMissouriUnited States
Clinical Site 125LincolnNebraskaUnited States
Clinical Site 110Las VegasNevadaUnited States
Clinical Site 101MarltonNew JerseyUnited States
Clinical Site 148Toms RiverNew JerseyUnited States
Clinical Site 128New YorkNew YorkUnited States
Clinical Site 102Staten IslandNew YorkUnited States
Clinical Site 111HickoryNorth CarolinaUnited States
Clinical Site 143RaleighNorth CarolinaUnited States
Clinical Site 138Middleburg HeightsOhioUnited States
Clinical Site 127North CantonOhioUnited States
Clinical Site 106MediaPennsylvaniaUnited States
Clinical Site 118PhiladelphiaPennsylvaniaUnited States
Clinical Site 114Fort WorthTexasUnited States
Clinical Site 109HoustonTexasUnited States
Clinical Site 149Missouri CityTexasUnited States
Clinical Site 144PlanoTexasUnited States
Clinical Site 147DraperUtahUnited States
Clinical Site 135BellevueWashingtonUnited States
Clinical Site 150San JuanPuerto Rico

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT04103892 on ClinicalTrials.gov →

Last updated in the registry 2025-10-14. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits