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Trial record 2 of 32 for:    cleo

CLE-100 as an Oral Therapy in Addition to Standard Antidepressant Drug for Major Depressive Disorder - CLEO Study

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ClinicalTrials.gov Identifier: NCT04103892
Recruitment Status : Recruiting
First Posted : September 26, 2019
Last Update Posted : June 11, 2021
Sponsor:
Information provided by (Responsible Party):
Clexio Biosciences Ltd.

Brief 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.

Condition or disease Intervention/treatment Phase
Adjunctive Treatment of Major Depressive Disorder Drug: CLE-100 Drug: placebo Phase 2

Detailed Description:

CLEO study is performed in two parts (part A and Part B). The sponsor is currently recruiting only for the Part B of the study.

Part A will be an inpatient study to assess the safety, tolerability, and pharmacokinetics of CLE-100 in MDD participants currently treated with an antidepressant drug. It will include a screening phase (up to 35 days), a 1 week inpatient double-blind treatment phase and an outpatient post treatment safety follow-up phase of 1 week after last study drug administration.

Part B will be a study to assess the safety and efficacy of CLE-100 in MDD participants currently treated with an antidepressant drug with inadequate response to standard antidepressant therapy.

The participants will remain on their current antidepressant therapy with no dose change during the study.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 137 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Part A - 15 patients, 2 arms, parallel; Part B - 122 patients, 2 arms, parallel
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Official Title: A Two-Part Study of CLE-100 as an Adjunct Therapy in Subjects With Major Depressive Disorder
Actual Study Start Date : September 5, 2019
Estimated Primary Completion Date : November 15, 2021
Estimated Study Completion Date : November 30, 2021

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Antidepressants

Arm Intervention/treatment
Experimental: CLE-100

Part A: 1 oral tablet of CLE-100 once daily (in addition to current anti-depressant drug) for 1 week.

Part B: 1 oral tablet of CLE-100 once daily (in addition to current anti-depressant drug) for 4 weeks.

Drug: CLE-100
1 tablet of CLE-100 administered once daily

Placebo Comparator: placebo

Part A: 1 oral tablet of Placebo once daily (in addition to current anti-depressant drug) for 1 week.

Part B: 1 oral tablet of Placebo once daily (in addition to current anti-depressant drug) for 4 weeks.

Drug: placebo
1 tablet of placebo administered once daily




Primary Outcome Measures :
  1. Part A - Frequency of adverse events [ Time Frame: 14 days ]
  2. Part A - Self-Administered Karolinska Sleepiness Scale [ Time Frame: 7 days ]
    The Karolinska Sleepiness Scale is a single-item, subjective, self-reported instrument measuring sleepiness on a 9-point Likert scale (1 to 9), where a higher value represents a worse outcome.

  3. Part A - Modified Observer's Assessment of Alertness/Sedation Scale (MOAA/S) [ Time Frame: 7 days ]
    The MOAA/S will be used to measure treatment-emergent sedation. The MOAA/S is a widely used clinician-administered measure of alertness/sedation for clinical trials. The MOAA/S measures the alertness/sedation spectrum on a 6-point scale (0 to 5) based on verbal cues, where a higher value represents a better outcome.

  4. Part A - Clinician-Administered Dissociative Symptoms Scale (CADSS) [ Time Frame: 7 days ]
    The CADSS will be administered to assess treatment-emergent dissociative symptoms. The CADSS is a 23-item instrument that is clinician-administered. Each item is scored on a 5-point scale (0 to 4. A higher value represents a worse outcome. The CADSS total score ranges between 0 and 92.

  5. Part A - Columbia Suicide Severity Rating Scale (C-SSRS) [ Time Frame: 7 days ]
    The C-SSRS will be performed to assess suicidal ideation and behavior. The C-SSRS is an instrument used to assess suicide risk by measuring symptoms of suicidal ideation, self-harm, and suicidal behavior that is administered by trained personnel. The suicidal ideation is evaluated with a "yes/no" questionnaire and the suicidal behavior severity is scored on a 6-point scale (0 to 5) where a higher value represents a more severe behavior.

  6. Part A - Four-items positive subscale from the Brief Psychiatric Rating Scale (BPRS) [ Time Frame: 7 days ]
    Four items of the BPRS will be administered to assess treatment-emergent psychotic symptoms. The BPRS is a widely used, clinician-administered instrument that involves 4 subscales: Negative Symptoms, Positive Symptoms, Manic-Hostility, and Anxiety/Depression. The 4-item Positive Symptoms subscale of the BPRS will be used to screen for potential psychiatric symptoms (suspiciousness, hallucinations, unusual thought content, and conceptual disorganization). Each item is scored on a 7-point scale (1 to 7). where a higher value represents a worse outcome. The 4 items BPRS total score ranges between 4 and 28.

  7. Part A - 20-item Physician Withdrawal Checklist (PWC-20) [ Time Frame: 14 days ]
    The PWC-20 is a clinician-administered assessment to evaluate potential withdrawal symptoms following cessation of the double-blind treatment. The PWC-20 is a shortened version of the original 35-item instrument used to determine withdraw symptoms in subjects following discontinuation of anxiolytics. The items are evaluated on a 4-point scale (0 to 3) where a higher value represents a worse outcome. The total score ranges between 0 to 60.

  8. Part A - Cognitive function evaluated by Cogstate battery [ Time Frame: 7 days ]
    The Cogstate battery of cognitive tests will be used to measure psychomotor function, attention, visual learning, and working memory. The Cogstate battery will include the following tests: Detection Test, Identification Test, One Back Test, Groton Maze Test.

  9. Part A - Digit Symbol Substitution Test (DSST) [ Time Frame: 7 days ]
    The DSST is a psychometric test assessing the integrity of executive function, processing speed, attention, spatial perception, and visual scanning, which are functions required for driving, and will be performed repeatedly. The DSST is a valid and sensitive instrument to evaluate cognitive dysfunction and changes in cognitive function. The DSST is a timed test taken by the subject and scored based on both the number of correct answers and the speed at which they were determined. The score ranges between 0 to 135.

  10. Part A - Pharmacokinetics of CLE-100 (Cmax) [ Time Frame: 7 days ]
    Maximum observed plasma concentration (Cmax)

  11. Part A - Pharmacokinetics of CLE-100 (Tmax) [ Time Frame: 7 days ]
    Time of maximum observed plasma concentration (Tmax)

  12. Part A - Pharmacokinetics of CLE-100 (AUC) [ Time Frame: 8 days ]
    Area under the concentration curve

  13. Part B - Change from baseline in Montgomery-Asberg Depression Rating Scale (MADRS) score [ Time Frame: 29 days ]
    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.


Secondary Outcome Measures :
  1. Part B - Change from baseline in Symptoms of Depression Questionnaire (SDQ) score [ Time Frame: 29 days ]
    The SDQ is a 44-item self-report scale for the assessment of MDD that includes assessments for irritability, anger attacks, and anxiety symptoms. Higher scores represent a more severe condition.

  2. Part B - Change from baseline in Sheehan Disability Scale (SDS) [ Time Frame: 29 days ]
    The SDS is a 3-item, self-completion instrument to assess functional impairments associated with work/school, social life and leisure activities, and family life and home responsibilities utilizing a 10-point scale.

  3. Part B - Change from baseline in Montgomery-Asberg Depression Rating Scale (MADRS) score [ Time Frame: 15 days ]
    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.

  4. Part B - Change from baseline in Clinical Global Impression - Severity (CGI-S) score [ Time Frame: 29 days ]
    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.



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

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 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 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. Has a lifetime history of any substance use disorder per DSM-5 criteria, except for tobacco use disorder.
  4. Has a history or current diagnosis of bipolar disorder, schizophrenia, or schizoaffective disorders.
  5. Has a current binge eating disorder or history of (binge) eating disorders within 1 year of Screening.
  6. Has dementia, delirium, amnesia, or any other significant cognitive disorder.
  7. Has posttraumatic stress disorder, obsessive compulsive disorder, or any other mental disorder (including personality disorders).
  8. Has any medical condition for which an increase in blood pressure or intracranial pressure poses a serious risk.
  9. Has been randomized in Part A of this study.
  10. Is a female of childbearing potential pregnant or breastfeeding.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04103892


Contacts
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Contact: Clinical Operations Lead 972-73-3318717 cleo.study@clexio.com

Locations
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Sponsors and Collaborators
Clexio Biosciences Ltd.
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Responsible Party: Clexio Biosciences Ltd.
ClinicalTrials.gov Identifier: NCT04103892    
Other Study ID Numbers: CLE100-MDD-201
First Posted: September 26, 2019    Key Record Dates
Last Update Posted: June 11, 2021
Last Verified: June 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Clexio Biosciences Ltd.:
MDD
depression
depressive disorder
major depression
adjunct therapy
oral
Additional relevant MeSH terms:
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Disease
Depressive Disorder
Depression
Depressive Disorder, Major
Pathologic Processes
Mood Disorders
Mental Disorders
Behavioral Symptoms