Overview

A Study to Assess the Effects of Multiple-Dose Probenecid on the Multiple-Dose Pharmacokinetics of Canagliflozin in Healthy Volunteers

Status:
Completed
Trial end date:
2011-10-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to assess the effects of multiple doses of probenecid on the multiple-dose pharmacokinetics of canagliflozin and its metabolites in healthy volunteers. Safety and tolerability will also be assessed.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Treatments:
Canagliflozin
Probenecid
Criteria
Inclusion Criteria: Body mass index (BMI) between 18 and 28 kg/m² inclusive and a body
weight of not less than 50 kg. Exclusion Criteria:History of or current medical illness,
abnormal values for hematology or clinical chemistry laboratory tests, or abnormal physical
examination, vital signs or 12-lead electrocardiogram (ECG) deemed to be clinically
significant by the Investigator