Study ITI-007-035 is a Phase 1b, multicenter, open-label study to evaluate the safety, tolerability, and PK of lumateperone for pediatric patients with Autism Spectrum Disorder.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
33
Lumateperone 10.5 mg capsule, oral administration
Lumateperone 21 mg capsule, oral administration
Lumateperone 5 mg ODT, oral administration
APG Research LLC
Orlando, Florida, United States
CenExeli Research LLC
Atlanta, Georgia, United States
Atlanta Center for Medical Research
Atlanta, Georgia, United States
CenExeli Research LLC 1
Savannah, Georgia, United States
Pharmacokinetics: Cmax
Maximum plasma concentration of lumateperone
Time frame: Day 5
Pharmacokinetics: Tmax
Time of maximum plasma concentration of lumateperone
Time frame: Day 5
Pharmacokinetics: AUC0-tau
Area under the plasma lumateperone concentration time curve from time zero to the end of dosing (tau)
Time frame: Day 5
Percentage of patients with treatment-emergent adverse events
Time frame: Up to 30 days after last dose
Change from baseline in systolic and diastolic blood presssure
Time frame: Day 6
Change from baseline in ECG QT interval
Time frame: Day 6
Change from baseline in hemoglobin
Time frame: Day 6
Change from baseline in white blood cell count
Time frame: Day 6
Change from baseline in aspartate aminotransferase
Time frame: Day 6
Change from baseline in alanine aminotransferase
Time frame: Day 6
Change from baseline in Abnormal Involuntary Movement Scale (AIMS)
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Lumateperone 10.5 mg ODT, oral administration
Lumateperone 5 mg ODT + 10.5 mg ODT, oral administration
Lumateperone 21 mg ODT, oral administration
Midwest Research Group
Saint Charles, Missouri, United States
Alivation Research LLC
Lincoln, Nebraska, United States
Core Clinical Research
Everett, Washington, United States
AIMS is a measure of facial and oral movements, extremity movements and trunk movements. Items are rated on a scale from none (0) to severe (4).
Time frame: Day 6