The main aim of the study is to test the safety and tolerability of single doses of SPL026 (N,N-dimethyltryptamine \[DMT\] fumarate, a psychedelic tryptamine) in patients currently taking a selective serotonin reuptake inhibitor (SSRI) for their depression, but for whom the SSRI is not fully relieving their depression.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
18
Intravenous
Mac Clinical Research
Manchester, Greater Manchester, United Kingdom
MAC Clinical Research
Liverpool, Prescot, United Kingdom
Safety & tolerability: Adverse Events
Adverse events (AEs)
Time frame: Screening to End-of-Study Follow-up (Day 29)
Safety & tolerability: Lab biochemistry
Values of potential clinical importance
Time frame: Screening, Day -1 and Day 1
Safety & tolerability: Vital signs - Heart Rate
Heart rate
Time frame: Screening to Day 2
Safety & tolerability: Vital signs - Blood pressure
Blood pressure
Time frame: Screening to Day 2
Safety & tolerability: Vital signs - Temperature
Temperature
Time frame: Screening to Day 2
Safety & tolerability: Electrocardiogram
QTcX intervals
Time frame: Screening to Day 2
Safety & tolerability: Suicidal Ideation
Columbia-Suicide Severity Rating Scale
Time frame: Screening to End-of-Study Follow-up (Day 29)
Evaluation of plasma levels of DMT
Pharmacokinetic parameter calculation in the Test Cohort compared to the Control Cohort
Time frame: 2, 5, 7, 10, 11, 13, 15, 30, 60, 120, 240 minutes post-dose
Mystical Experience Questionnaire (MEQ)
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MEQ in the Test Cohort compared to the Control Cohort
Time frame: Day 1 (dosing day)
Challenging Experience Questionnaire (CEQ)
CEQ in the Test Cohort compared to the Control Cohort
Time frame: Day 1 (dosing day)
Ruminative Responses Scale (RRS)
RRS in the Test Cohort compared to the Control Cohort
Time frame: Day -1 and Day 29
Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS)
WEMWBS in the Test Cohort compared to the Control Cohort
Time frame: Day -1, Day 15 and Day 29