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CompletedPhase 2Results posted

A Study of CLE-100 (Oral Esketamine) as an Adjunctive Treatment to Standard Antidepressants for Major Depressive Disorder

NCT06340958 · SOLEO · Clexio Biosciences Ltd.

Closed to entry
Status
Not accepting participants
Phase 2
Phase
99
Target enrolment
23
Study sites
13 US states

What it is testing

Summary

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.

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

  • 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
Inclusion Criteria: 1. Male or female between 18 to 65 years of age at Screening 2. Diagnosis of MDD, single or recurrent, without psychotic features, in the current or previous episode(s), according to the Diagnostic and Statistical Manual of Mental Disorders-5 (DSM-5). The diagnosis of MDD must be supported by the Mini International Neuropsychiatric Interview (MINI) Screen 7.0.2 for DSM-5. 3. Currently experiencing a Major Depressive Episode (MDE) that began at least 12 weeks but no more than 5 years prior to Screening. The current MDE must be confirmed by the independent SAFER assessor. 4. MADRS score of 24 or higher at Screening as confirmed by an independent SAFER assessor. 5. At Screening, a history of inadequate response to at least 2 antidepressant medications in the current MDE. Inadequate response is defined as less than 50% improvement of depression symptoms following at least 6 weeks of treatment with a therapeutic dose and is assessed by the site using the Massachusetts General Hospital Antidepressant Treatment Response Questionnaire (MGH-ATRQ). Inadequate response to at least 2 antidepressant medications must be verified by documented medical or pharmacy records and confirmed by an independent SAFER assessor. 6. Able and competent to read and sign the informed consent form (ICF). Exclusion Criteria: 1. 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 and confirmed by the independent SAFER assessor. 2. A high risk of suicide based on any of the following: 1. Item 10 of MADRS score (suicidal thoughts) is 5 or higher at Screening or Baseline. 2. Suicide attempt in the previous 6 months. 3. Significant risk, as judged by the Investigator, based on the psychiatric interview or information collected with the C SSRS at Screening or Baseline. 3. 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 disorder or history within 12 months prior to Screening (Substance Use Disorder is diagnosed per DSM-5 criteria and does not include tobacco use disorder). 4. Use of ketamine, esketamine, PCP, or dextromethorphan recreationally in the past 6 months. 5. History or current diagnosis of bipolar disorder, schizophrenia, or schizoaffective disorder or other schizophrenia spectrum disorders. 6. Dementia, delirium, amnesia, or any other significant cognitive disorder. 7. Any medical condition for which an increase in blood pressure or intracranial pressure or intraocular pressure or tachycardia poses a serious risk (e.g., aneurysmal vascular disease, arteriovenous malformation, or history of intracerebral hemorrhage).

Where

23 study sites

FacilityCityRegionCountry
Clinical Site 139La JollaCaliforniaUnited States
Clinical Site 131LafayetteCaliforniaUnited States
Clinical Site 130UplandCaliforniaUnited States
Clinical Site 102HollywoodFloridaUnited States
Clinical Site 105LauderhillFloridaUnited States
Clinical Site 140Miami SpringsFloridaUnited States
Clinical Site 132PensacolaFloridaUnited States
Clinical Site 118AtlantaGeorgiaUnited States
Clinical Site 138MariettaGeorgiaUnited States
Clinical Site 114SavannahGeorgiaUnited States
Clinical Site 127ChicagoIllinoisUnited States
Clinical Site 120ElginIllinoisUnited States
Clinical Site 108GaithersburgMarylandUnited States
Clinical Site 116FlowoodMississippiUnited States
Clinical Site 126O'FallonMissouriUnited States
Clinical Site 101Toms RiverNew JerseyUnited States
Clinical Site 103BeachwoodOhioUnited States
Clinical Site 119North CantonOhioUnited States
Clinical Site 135Oklahoma CityOklahomaUnited States
Clinical Site 107AustinTexasUnited States
Clinical Site 137PlanoTexasUnited States
Clinical Site 117MurrayUtahUnited States
Clinical Site 115BellevueWashingtonUnited States

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.

NCT06340958 on ClinicalTrials.gov →

Last updated in the registry 2026-06-23. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits