Clinical Trials Directory

Trials / Completed

CompletedNCT01438359

A Drug-Drug Interaction Study of Furosemide and PA21

A Single-centre, Open-label, Three-period Study of the Pharmacokinetic Effect of PA21 on Furosemide in Healthy Male and Female Adults

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
42 (estimated)
Sponsor
Vifor Pharma · Industry
Sex
All
Age
20 Years – 50 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine if Furosemide is affected by PA21.

Conditions

Interventions

TypeNameDescription
DRUGPA21 and Furosemide with foodThe maximum dose of PA21 will be 15.0 g/day. The maximum dose of Furosemide will be 40 mg/day
DRUGNo PA21; Furosemide with foodThe maximum dosage of Furosemide will be 40 mg/day
DRUGPA21 with food and Furosemide 2hrs laterThe maximum dose of PA21 will be 15 g/day. The maximum dose of Furosemide will be 40 mg/day

Timeline

Start date
2011-07-01
Primary completion
2011-09-01
Completion
2011-09-01
First posted
2011-09-22
Last updated
2011-09-30

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01438359. Inclusion in this directory is not an endorsement.