Overview

Evaluation Study of the Bioavailability of Brexpiprazole Orally Disintegrating Tablets in Healthy Male Subjects

Status:
Completed
Trial end date:
2016-11-27
Target enrollment:
0
Participant gender:
Male
Summary
The ratios of the geometric means of the ODT formulation to those of the reference formulation (conventional tablet) for the bioavailability variables (Cmax, AUCt, and AUC∞ of brexpiprazole (OPC-34712)).
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Otsuka Pharmaceutical Co., Ltd.
Treatments:
Brexpiprazole
Criteria
Inclusion Criteria:

- Capable of providing written informed consent prior to initiation of any trial-related
procedures, and able, in the opinion of the investigator, to comply with all
requirements of the trial

Exclusion Criteria:

- Clinically significant abnormality at the time of screening (eg, significant deviation
from reference ranges) or in medical history that, in the opinion of investigator or
sponsor may place the subject at risk or interfere with outcome variables, including
drug absorption, distribution, metabolism, and excretion

- History of serious mental disorder

- History of drug or alcohol abuse within 2 years prior to screening

- History of any significant drug allergy

- Use of an investigational drug within 120 days prior to the first dosing of trial drug

- Use of tobacco products or daily exposure to secondhand smoke within 2 months prior to
screening

- Consumption of grapefruit, grapefruit products, Seville oranges, Seville orange
products, starfruit, or starfruit products within 72 hours prior to dosing

- Use of prescription, over-the-counter, or herbal medication, vitamin supplements, or
St. John's Wort within 14 days prior to the first dosing of trial drug, or of
antibiotics within 30 days prior to the first dosing of trial drug

- History of major surgery of the digestive tract (excluding appendectomy)

- Any subject who, in the opinion of the investigator, should not participate in the
trial