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
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 37
- 试验地点
- 1
- 主要终点
- Pharmacokinetics: Terminal elimination half-life (T1/2) of lumateperone and metabolites
研究概览
简要总结
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Sequential
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 50 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female patients aged 18 to 50 years, inclusive
- •Clinical diagnosis of schizophrenia according to Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5)
- •Clinically stable and free from acute exacerbation of psychosis for at least 3 months prior to Screening per Investigator assessment
- •On a stable dose of antipsychotic medication, including lumateperone, for at least 3 months prior to the Screening Visit
- •Clinical Global Impression - Severity (CGI-S) score ≤ 3
排除标准
- •Clinically significant abnormality within 2 years of Screening that, in the Investigator's opinion, may place the patient at risk or interfere with study outcome variables
- •History of psychiatric condition other than schizophrenia that, in the Investigator's opinion, may be detrimental to participation in the study
- •Any suicidal ideation within the 6 months prior to Screening, any suicidal behavior within 2 years prior to Screening based on the Columbia-Suicide Severity Rating Scale (C-SSRS) (excluding self-injurious, non-suicidal behavior), and/or Investigator assessment that the patient is a safety risk to him/herself or others
- •Surgical or medical condition (active or chronic) that in the Investigator's opinion may interfere with drug absorption, distribution, metabolism, or excretion of the study drug or any other condition that may place the patient at risk; history of gastric bypass or sleeve gastrectomy; history of severe dystonic reaction on antipsychotics such as laryngeal spasm
研究组 & 干预措施
Cohort 1: LAI Lumateperone 50 mg SC in the abdomen
干预措施: Lumateperone Long-Acting Injectable (Drug)
Cohort 2: LAI Lumateperone 100 mg SC in the abdomen
干预措施: Lumateperone Long-Acting Injectable (Drug)
Cohort 3: LAI Lumateperone 200 mg SC in the abdomen
干预措施: Lumateperone Long-Acting Injectable (Drug)
Cohort 4: LAI Lumateperone 100 or 200 mg SC in the outer area of the upper arm
干预措施: Lumateperone Long-Acting Injectable (Drug)
结局指标
主要结局
Pharmacokinetics: Terminal elimination half-life (T1/2) of lumateperone and metabolites
时间窗: predose and at multiple timepoints up to 7 weeks postdose
Pharmacokinetics: Area under the plasma concentration-time curve from time zero to the last measurable concentration (AUC0-t) of lumateperone and metabolites
时间窗: predose and at multiple timepoints up to 7 weeks postdose
Pharmacokinetics: Time of maximum observed plasma concentration (Tmax) of lumateperone and metabolites
时间窗: predose and at multiple timepoints up to 7 weeks postdose
Pharmacokinetics: Area under the plasma concentration-time curve (AUC0-t,SR) of lumateperone and metabolites during sustained-release phase
时间窗: predose and at multiple timepoints up to 7 weeks postdose
Pharmacokinetics: Area under the plasma concentration-time curve from time zero extrapolated to infinity (AUC0-inf) of lumateperone and metabolites
时间窗: predose and at multiple timepoints up to 7 weeks postdose
Pharmacokinetics: Maximum observed plasma concentration (Cmax) of lumateperone and metabolites
时间窗: predose and at multiple timepoints up to 7 weeks postdose
Pharmacokinetics: Maximum observed plasma concentration (Cmax,BR) of lumateperone and metabolites during burst-release phase
时间窗: predose and at multiple timepoints up to 7 weeks postdose
Pharmacokinetics: Time of maximum observed plasma concentration (Tmax,BR) of lumateperone and metabolites during burst-release phase
时间窗: predose and at multiple timepoints up to 7 weeks postdose
Pharmacokinetics: Area under the plasma concentration-time curve (AUC0-t,BR) of lumateperone and metabolites during burst-release phase
时间窗: predose and at multiple timepoints up to 7 weeks postdose
Pharmacokinetics: Maximum observed plasma concentration (Cmax,SR) of lumateperone and metabolites during sustained-release phase
时间窗: predose and at multiple timepoints up to 7 weeks postdose
Pharmacokinetics: Time of maximum observed plasma concentration (Tmax,SR) of lumateperone and metabolites during sustained-release phase
时间窗: predose and at multiple timepoints up to 7 weeks postdose
次要结局
- Change from baseline in Systolic and Diastolic Blood Pressure(up to 7 weeks postdose)
- Change from baseline in white blood cell count(up to 7 weeks postdose)
- Change from baseline in alanine aminotransferase(up to 7 weeks postdose)
- Change from baseline in hemoglobin(up to 7 weeks postdose)
- Percentage of participants with treatment-emergent AEs(up to 7 weeks postdose)
- Change from baseline in platelet count(up to 7 weeks postdose)
- Change from baseline in aspartate aminotransferase(up to 7 weeks postdose)
- Change from baseline in creatine kinase(up to 7 weeks postdose)
- Change from baseline in Abnormal Involuntary Movement Scale(up to 7 weeks postdose)
- Change from baseline in glucose(up to 7 weeks postdose)
- Change from baseline in ECG QT Interval(up to 7 weeks postdose)