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

Last updated: March 6, 2025
Sponsor: Clexio Biosciences Ltd.
Overall Status: Active - Recruiting

Phase

2

Condition

Depression

Treatment

Placebo

CLE-100

Clinical Study ID

NCT06340958
CLE100-MDD-202
  • Ages 18-65
  • All Genders

Study 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.

Eligibility Criteria

Inclusion

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 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.

  3. 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.

  4. MADRS score of 24 or higher at Screening as confirmed by an independent SAFERassessor.

  5. 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.

  6. Able and competent to read and sign the informed consent form (ICF).

Exclusion

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 andconfirmed by the independent SAFER assessor.

  1. A high risk of suicide based on any of the following:

  2. Item 10 of MADRS score (suicidal thoughts) is 5 or higher at Screening orBaseline.

  3. Suicide attempt in the previous 6 months.

  4. Significant risk, as judged by the Investigator, based on the psychiatricinterview or information collected with the C SSRS at Screening or Baseline.

  5. 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).

  6. Use of ketamine, esketamine, PCP, or dextromethorphan recreationally in the past 6months.

  7. History or current diagnosis of bipolar disorder, schizophrenia, or schizoaffectivedisorder or other schizophrenia spectrum disorders.

  8. Dementia, delirium, amnesia, or any other significant cognitive disorder.

  9. 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

Total Participants: 90
Treatment Group(s): 2
Primary Treatment: Placebo
Phase: 2
Study Start date:
March 18, 2024
Estimated Completion Date:
January 10, 2026

Study Description

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.

Connect with a study center

  • Clinical Site 139

    La Jolla, California 92037
    United States

    Active - Recruiting

  • Clinical Site 131

    Lafayette, California 94549
    United States

    Active - Recruiting

  • Clinical Site 130

    Upland, California 91786
    United States

    Active - Recruiting

  • Clinical Site 102

    Hollywood, Florida 33024
    United States

    Active - Recruiting

  • Clinical Site 105

    Lauderhill, Florida 33319
    United States

    Active - Recruiting

  • Clinical SIte 112

    Miami Lakes, Florida 33016
    United States

    Site Not Available

  • Clinical Site 140

    Miami Springs, Florida 33166
    United States

    Active - Recruiting

  • Clinical Site 132

    Pensacola, Florida 32502
    United States

    Active - Recruiting

  • Clinical Site 118

    Atlanta, Georgia 30030
    United States

    Active - Recruiting

  • Clinical Site 138

    Marietta, Georgia 30060
    United States

    Active - Recruiting

  • Clinical Site 114

    Savannah, Georgia 31405
    United States

    Active - Recruiting

  • Clinical Site 127

    Chicago, Illinois 60640
    United States

    Site Not Available

  • Clinical Site 120

    Elgin, Illinois 60123
    United States

    Active - Recruiting

  • Clinical Site 108

    Gaithersburg, Maryland 20877
    United States

    Active - Recruiting

  • Clinical Site 116

    Flowood, Mississippi 39232
    United States

    Active - Recruiting

  • Clinical Site 126

    O'Fallon, Missouri 63368
    United States

    Active - Recruiting

  • Clinical Site 128

    Marlton, New Jersey 08054
    United States

    Site Not Available

  • Clinical Site 101

    Toms River, New Jersey 08755
    United States

    Active - Recruiting

  • Clinical Site 133

    New York, New York 10036
    United States

    Site Not Available

  • Clinical Site 103

    Beachwood, Ohio 44236
    United States

    Active - Recruiting

  • Clinical Site 119

    North Canton, Ohio 44720
    United States

    Active - Recruiting

  • Clinical Site 135

    Oklahoma City, Oklahoma 73112
    United States

    Site Not Available

  • Clinical Site 107

    Austin, Texas 78737
    United States

    Active - Recruiting

  • Clinical Site 106

    DeSoto, Texas 75115
    United States

    Site Not Available

  • Clinical Site 137

    Plano, Texas 75093
    United States

    Active - Recruiting

  • Clinical Site 117

    Murray, Utah 84107
    United States

    Active - Recruiting

  • Clinical Site 115

    Bellevue, Washington 98007
    United States

    Active - Recruiting

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