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
26
Lumateperone 10.5 mg capsule, oral administration
Lumateperone 21 mg capsule, oral administration
Lumateperone 5 mg ODT, oral administration
Clinical Site 6
Miami, Florida, United States
NOT_YET_RECRUITINGClinical Site 7
Orlando, Florida, United States
NOT_YET_RECRUITINGClinical Site 1
Atlanta, 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
Clinical Site 2
Decatur, Georgia, United States
RECRUITINGClinical Site 3
Savannah, Georgia, United States
RECRUITINGClinical Site 4
Saint Charles, Missouri, United States
RECRUITINGClinical Site 5
Lincoln, Nebraska, United States
RECRUITINGClinical Site 8
Everett, Washington, United States
RECRUITINGAIMS 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