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NCT Number: NCT03734302

The Pharmacokinetics, and Safety of Brexpiprazole Tablets in Chinese Healthy Subjects

This study is a single-center, open-label study evaluating the pharmacokinetics and safety of multiple dose oral administration of Brexpiprazole (1 mg) tablets in Chinese healthy subject.10 healthy adult subjects will be enrolled in this study. A single dose (Brexpiprazole 1 mg) group is set and the test drug will be administered for 14 consecutive days.

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Key information

Conditions

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Beijing Anding Hospital of Capital Medical University

Beijing, Beijing Municipality, 100088, China

About this study

10 healthy adult subjects will be enrolled in this study. A single dose (Brexpiprazole 1 mg) group is set and the test drug will be administered for 14 consecutive days.

After receiving the informed consent form the subject themselves, the investigators start the screening 14 days to 1 days prior to taking the study drug (D-14 to D-1).

One day before first dosing (D-1), subjects are hospitalized. On the next day (D1), after completed the hospitalization inspection, eligible subjects will be selected to start with the first dose, and from day 1 to day 14 (D1 to D14), continue once daily dosing and complete the corresponding inspection, observation and blood sampling. They continue hospitalization and are discharged on day 17 (D17) after completing the relevant examinations. On days 19, 21, 23,25 (D19, D21,D23 and D25), blood samples are collected and safety evaluation is performed.

Telephone follow-up is performed on day 44 (D44, 30 days after the last dose of the drug).

Subjects who early terminated the test after taking the study drug should be tested at the end of the study (D25/ET) as far as possible.

Blood samples for pharmacokinetic evaluation are collected before daily dosing; D1 (before dosing, and 1, 2, 3, 4, 5, 6, 8, 12 hours after dosing), D2 (before dosing and 24 hours after first dosing), D10 (before dosing), D11 (before dosing), D12 (before dosing), D13 (before dosing), D14 (before dosing, and 1, 2, 3, 4, 5, 6, 8, 12 hours after dosing), D15 (24 hours after last dosing), D16 (48 hours after last dosing), D17 (72 hours after last dosing), D18 (96 hours after last dosing), D19 (120 hours after last dosing), D21 (168 hours after last dosing),D23 (216 hours after last dosing), D25 (264 hours after last dosing). 31 Blood samples collecting points in total.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 1. Sign the informed consent form
  • 2. At the age of 18~45 years old (including upper and lower limits).
  • 3. Body weight of not less than 45 kg, body mass index 19 ~ 25kg/m2 range (including the upper and lower limits) [ body mass index (BMI) = body weight (kg) / height2 (m2)].

Exclusion criteria

  • 1. Participated in any drug test within 12 weeks prior to enrollment.
  • 2. Drug abuse in the past 2 years or a history of substance abuse.
  • 3. Drinking alcohol more than 2 unit per day (1 unit= 360 ml beer , or 45 ml 4.0% alcohol, or 150 ml liquor, or 50 ml wine ) 6 months before the screening, or subjects can not stop drinking during the hospitalization.
  • 4. Drug abuse urine test at screening is positive.

Other protocol-defined inclusion and exclusion criteria may apply.

Treatment and study plan

Brexpiprazole

Drug

Brexpiprazole , mutiple dose /oral/empty stomach

Other names: Brex

Primary outcomes

  1. Steady-state peak time (Tss_max)

    Time frame: Day1, Day2, Day10, Day11, Day12, Day13, Day14, Day15, Day16, Dv17, Day18, Day19, Dv21,Day23, Day25

    Assessment of the steady-state peak time of Brexpiprazole

  2. Steady-state valley concentration(Css_min)

    Time frame: Day1, Day2, Day10, Day11, Day12, Day13, Day14, Day15, Day16, Dv17, Day18, Day19, Dv21,Day23, Day25

    Assessment of the steady-state valley concentration of Brexpiprazole

  3. Steady-state peak concentration (Css_max)

    Time frame: Day1, Day2, Day10, Day11, Day12, Day13, Day14, Day15, Day16, Dv17, Day18, Day19, Dv21,Day23, Day25

    Assessment of the steady-state peak concentration of Brexpiprazole

  4. Average steady-state plasma concentration (Css_av)

    Time frame: Day1, Day2, Day10, Day11, Day12, Day13, Day14, Day15, Day16, Dv17, Day18, Day19, Dv21,Day23, Day25

    Assessment of the average steady-state plasma concentration (Css_av) of Brexpiprazole

  5. Half-life (t1/2, z)

    Time frame: Day1, Day2, Day10, Day11, Day12, Day13, Day14, Day15, Day16, Dv17, Day18, Day19, Dv21,Day23, Day25

    Assessment of the Half-life of Brexpiprazole

  6. Steady-state clearance (CLss/F)

    Time frame: Day1, Day2, Day10, Day11, Day12, Day13, Day14, Day15, Day16, Dv17, Day18, Day19, Dv21,Day23, Day25

    Assessment of the steady-state clearance of Brexpiprazole

  7. Area under steady state plasma concentration-time curve (AUC)ss

    Time frame: Day1, Day2, Day10, Day11, Day12, Day13, Day14, Day15, Day16, Dv17, Day18, Day19, Dv21,Day23, Day25

    Assessment of the area under steady state plasma concentration-time curve of Brexpiprazole

  8. Fluctuation index (DF)

    Time frame: Day1, Day2, Day10, Day11, Day12, Day13, Day14, Day15, Day16, Dv17, Day18, Day19, Dv21,Day23, Day25

    Assessment of the fluctuation index of Brexpiprazole

  9. Cumulative coefficient (RAUC, Rcmax)

    Time frame: Day1, Day2, Day10, Day11, Day12, Day13, Day14, Day15, Day16, Dv17, Day18, Day19, Dv21,Day23, Day25

    Assessment of the cumulative coefficient of Brexpiprazole

Secondary outcomes

  1. The peak concentration (Cmax) after the first administration

    Time frame: Day1, Day2

    The peak concentration (Cmax) of Brexipiprazole and the metabolite DM-3411 on the first day after administration are calculated.

  2. The peak time (Tmax) after the first administration

    Time frame: Day1, Day2

    The peak-time of Brexipiprazole and the metabolite DM-3411 on the first day after administration are calculated.

  3. Area under the plasma concentration-time curve (AUC0-24h)

    Time frame: Day1, Day2

    The area under the plasma concentration-time curve of Brexipiprazole and the metabolite DM-3411 on the first day after administration are calculated.

  4. Valley concentration points

    Time frame: Day10, Day11, Day12, Day13, Day14

    Descriptive statistics about the valley concentration points before taking the study drug on days 10, 11, 12, 13 and 14

Sponsors and collaborators

Lead sponsor

Otsuka Beijing Research Institute

Industry

Registry information

Official study title

A Single-center, Open-label Study Evaluating the Pharmacokinetics, and Safety of Multiple Dose Oral Brexpiprazole Tablets (1 mg) in Chinese Healthy Subjects

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Nov 7, 2018
Registry last updated
Nov 1, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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