Lenexa, Kansas 66219


Purpose:

This will be a single-center, multiple-dose, randomized, double-blind, placebo-controlled, positive-controlled, twelve sequence, 3-period cross-over study to investigate the effect of balovaptan on the QTc interval in healthy subjects.


Criteria:

Inclusion Criteria: - Healthy male and female subjects. Healthy status is defined by absence of evidence of any active or chronic disease following a detailed medical and surgical history, a complete physical examination including vital signs, 12-lead ECG, hematology, blood chemistry, urinalysis, and serology. - Body Mass Index of 18 to 30 kg/m2, inclusive. - For women of childbearing potential: agreement to use at least 1 acceptable form of contraception during the entire study and for 90 days following last dose of study drug. - For men: vasectomized, agreement to remain abstinent or use of a condom during intercourse. Must also agree to refrain from donating sperm. - Fluent in English. Exclusion Criteria: - If female, a positive pregnancy test at screening or prior to Day 1 of any Treatment Period. - Lactating women. - Any condition or disease detected during the medical interview / physical examination that would render the subject unsuitable for the study, place the subject at undue risk or interfere with the ability of the subject to complete the study in the opinion of the Investigator or designee.


NCT ID:

NCT03808298


Primary Contact:

Reference Study ID Number: WP40734 www.roche.com/about_roche/roche_worldwide.htm
Phone: 888-662-6728 (U.S. and Canada)
Email: global-roche-genentech-trials@gene.com


Backup Contact:

N/A


Location Contact:

Lenexa, Kansas 66219
United States



There is no listed contact information for this specific location.

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: February 04, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

If you would like to be contacted by the clinical trial representative please fill out the form below.