Lumateperone Long-Acting Injectable
DrugLumateperone Long-Acting Injectable
NCT Number: NCT04709224
This is an open-label study to determine the pharmacokinetics, safety and tolerability of single ascending doses of lumateperone long-acting injectable formulation in patients with schizophrenia. Patients will be enrolled in one of up to four cohorts. All patients will receive oral lumateperone for 5 days, followed by a 5-day washout of oral lumateperone, then followed by a single dose of lumateperone LAI.
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Notify Me18 year–50 year
All sexes
Interventional
Phase 1
Clinical Site, Long Beach, California, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
Lumateperone Long-Acting Injectable
Time frame: predose and at multiple timepoints up to 7 weeks postdose
Time frame: predose and at multiple timepoints up to 7 weeks postdose
Time frame: predose and at multiple timepoints up to 7 weeks postdose
Time frame: predose and at multiple timepoints up to 7 weeks postdose
Time frame: predose and at multiple timepoints up to 7 weeks postdose
Time frame: predose and at multiple timepoints up to 7 weeks postdose
Time frame: predose and at multiple timepoints up to 7 weeks postdose
Time frame: predose and at multiple timepoints up to 7 weeks postdose
Time frame: predose and at multiple timepoints up to 7 weeks postdose
Time frame: predose and at multiple timepoints up to 7 weeks postdose
Time frame: predose and at multiple timepoints up to 7 weeks postdose
Time frame: up to 7 weeks postdose
Time frame: up to 7 weeks postdose
Time frame: up to 7 weeks postdose
Time frame: up to 7 weeks postdose
Time frame: up to 7 weeks postdose
Time frame: up to 7 weeks postdose
Time frame: up to 7 weeks postdose
Time frame: up to 7 weeks postdose
Time frame: up to 7 weeks postdose
Time frame: up to 7 weeks postdose
Time frame: up to 7 weeks postdose
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).
Intra-Cellular Therapies, Inc.
Industry
An Open-label Study to Determine the Pharmacokinetics, Safety and Tolerability of Single Ascending Doses of a Subcutaneous Injection of Lumateperone Long-Acting Injectable (LAI) Formulation in Patients With Schizophrenia
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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