A Phase 1 Single Dose PK Study in Adolescent Subjects With Fragile X Syndrome or Angelman Syndrome
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 12
- 试验地点
- 1
- 主要终点
- Measurement of maximum plasma concentration achieved following a single dose of OV101
研究概览
简要总结
The trial is a Phase 1 Single Dose PK Study in Adolescent Subjects with Fragile X syndrome (FXS) or Angelman syndrome (AS).
- The primary objective of the study is to evaluate the pharmacokinetics (PK) of OV101 following a single 5 mg dose of OV101 in adolescents with FXS or AS.
- Secondary objectives are to determine the safety and tolerability of a single 5 mg dose of OV101 in adolescents with FXS or AS.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 13 Years 至 17 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adolescents with confirmed clinical and previous molecular diagnosis of FXS or AS, age between 13 to 17 years, inclusive.
- •Subjects must assent to participation in the study (if appropriate), have a parent or legal guardian/representative capable of providing informed consent on behalf of the subject, and commit to participate in all assessments described in the protocol.
- •Subjects must be receiving a stable dose of concomitant medications
- •Subjects should be able to complete study assessments.
- •Subjects who are non-sterile must agree to either remain completely abstinent or to use two effective contraceptive methods from screening until 7 days after the last dose of study treatment.
- •Subjects must have a parent or other reliable caregiver who agrees to accompany the subject at all study visits and provide information about the subject as required by the study protocol, and ensure compliance with the protocol.
排除标准
- •Inability to swallow a capsule.
- •Poorly controlled seizures
- •Clinically significant abnormal ECG at the time of screening.
- •Positive result on serum or urine pregnancy test for women of child-bearing potential (have experienced menarche) who are not using a dual method of contraception (e.g., condoms plus oral contraceptives), with abstinence being an accepted method.
- •Allergy to gaboxadol or any excipients
- •Concomitant cardiovascular, respiratory, liver, renal, or hematologic diseases of a degree that would limit participation in the study
- •History of suicidal behavior or considered a high suicidal risk by the investigator.
- •Any medical, psychological, social disorder(s), or other conditions - including seizure disorder
研究组 & 干预措施
Single-dose 5 mg OV101
干预措施: OV101 (Drug)
结局指标
主要结局
Measurement of maximum plasma concentration achieved following a single dose of OV101
时间窗: 10 hours
Maximum plasma concentration (Cmax)
Measurement of time of maximum plasma concentration following a single dose of OV101
时间窗: 10 hours
Time after administration of drug when maximum plasma concentration is reached (Tmax)
Measurement of plasma half-life following a single dose of OV101
时间窗: 10 hours
Plasma half-life (T1/2)
Measurement of the area under the plasma concentration versus time curve following a single dose of OV101
时间窗: 10 hours
Area under the curve from 0 to 10 hours (AUC 0-10)
Measurement of the apparent volume of distribution following a single dose of OV101
时间窗: 10 hours
Apparent volume of distribution during terminal phase (Vz)
Measurement of clearance following a single dose of OV101
时间窗: 10 hours
Total body clearance (CL)
次要结局
- Safety parameters, adverse events, absolute values and changes over time of hematology, clinical chemistry, urinalysis, vital signs, electrocardiogram (ECG)(10 hours)