Study ITI-007-020 is a Phase 1b, multicenter, open-label study to evaluate the safety, tolerability, and PK of lumateperone as treatment for adolescent patients with schizophrenia or schizoaffective disorder.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
26
Lumateperone 42 mg, oral administration
Lumateperone 28 mg, oral administration
Clinical Site
Hollywood, Florida, United States
Clinical Site
Atlanta, Georgia, United States
Clinical Site
Decatur, Georgia, United States
Pharmacokinetics: Cmax
Maximum plasma concentration of lumateperone
Time frame: Day 1 and Day 5
Pharmacokinetics: Tmax
Time of maximum concentration of lumateperone in plasma
Time frame: Day 1 and Day 5
Pharmacokinetics: AUC0-t
Area under the plasma concentration time curve from time zero to the last measurable of concentration of lumateperone
Time frame: 0 to 24 hours post-dose on Day 1 and Day 5
Pharmacokinetics: AUC0-tau
Area under the plasma lumateperone concentration time curve from time zero to the end of dosing (tau)
Time frame: 0 to 24 hours post-dose on Day 1 and Day 5
Pharmacokinetics: t1/2
Terminal elimination half-life of lumateperone
Time frame: Day 1 and Day 5
Pharmacokinetics: CL/F
Apparent oral clearance of lumateperone
Time frame: Day 1 and Day 5
Percentage of Subjects With Treatment-emergent Adverse Events
Time frame: up to 30 days after last dose, up to a total of 35 days
Change From Baseline in Systolic and Diastolic Blood Pressure
Time frame: Baseline and Day 6
Change From Baseline in ECG QT Interval
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QTcF
Time frame: Baseline and Day 6
Change From Baseline in Hemoglobin
Time frame: Baseline and Day 6
Change From Baseline in White Blood Cell Count
Time frame: Baseline and Day 6
Change From Baseline in Aspartate Aminotransferase
Time frame: Baseline and Day 6
Change From Baseline in Alanine Aminotransferase
Time frame: Baseline and Day 6
Change From Baseline in Abnormal Involuntary Movement Scale (AIMS)
AIMS is a measure of facial and oral movements, extremity movements and trunk movements. The AIMS total score is reported based on 7 items (items 1 through 7). Each item is rated on a scale from none (0) to severe (4). The AIMS total score ranges from 0 to 28. Higher values of total AIMS score indicate increased severity in abnormal movement.
Time frame: Baseline and Day 6