Phase 1
Completed N=74
Bioequivalence Between Single Administration of ASC-01 (Aripiprazole/Sertraline Combination Drug) and Concomitant Single Administration of Aripiprazole and Sertraline, and Food Effect on Pharmacokinetics of ASC-01 in Healthy Male Adults
Healthy Male Adults
Source: ClinicalTrials.gov NCT03342963 ↗
Enrolled (actual)
74
Serious AEs
0.0%
Results posted
May 2021
Primary outcomePrimary: Peak Plasma Concentration (Cmax) of Aripiprazole in Cohort 1 — 18.8; 16.9 ng/mL
Summary
To investigate the bioequivalence of aripiprazole between administration of one ASC-01 tablet (aripiprazole 3 mg/sertraline 100 mg combination drug) and concomitant administration of one aripiprazole 3-mg tablet and two sertraline 50-mg tablets (Cohort 1).
To investigate food effect on plasma pharmacokinetics of aripiprazole and sertraline by single oral administration of ASC-01 under a fasting or fed condition (Cohort 2).
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Peak Plasma Concentration (Cmax) of Aripiprazole in Cohort 1 |
18.8; 16.9 | — |
| PRIMARY Area Under the Plasma Concentration Versus Time Curve 168h (AUC168h) of Aripiprazole in Cohort 1 |
783; 779 | — |
| PRIMARY Cmax of Aripiprazole and Sertraline in Cohort 2 |
16.9; 16.6; 28.9; 36.5 | — |
| PRIMARY AUC168h of Aripiprazole and Sertraline in Cohort 2 |
701; 865; 904; 1060 | — |
Eligibility Criteria
Inclusion Criteria
- Healthy male subject at the age between 20 and 40 at the time of informed consent
- Subject has a body mass index (BMI = body weight [kg]/height [m]2) of ≥18.5 and <25.0 kg/m2 at screening
- Subject is providing consent for participation in this trial in writing prior to the start of the procedures related to this trial, and judged by the investigator or subinvestigator to be capable of observing procedures in this trial.
Exclusion Criteria
- Subject has a clinically significant abnormality in physical findings at screening or in medical history that in the investigator's or subinvestigator's opinion may place the subject at risk or interfere with outcome variables including drug absorption, distribution, metabolism, and excretion.
- Subject is judged by the investigator or subinvestigator to be inappropriate for participation in this trial.
Data sourced from ClinicalTrials.gov (NCT03342963). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.