RDEA3170 Tablet and Capsule Bioavailability Study

Study identifier:RDEA3170-111

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Recruitment Complete

Official Title

A Phase 1, Randomized, Open-Label, Study in Healthy Adult Male Subjects to Assess the Relative Bioavailability and Food Effect of Various Formulations of RDEA3170

Medical condition

Healthy

Phase

Phase 1

Healthy volunteers

Yes

Study drug

RDEA3170, 5mg, RDEA3170,10 mg, RDEA3170, 2.5 mg

Sex

Male

Actual Enrollment

20

Study type

Interventional

Age

18 Years - 65 Years

Date

Study Start Date: 01 May 2015
Primary Completion Date: 01 Jun 2015
Estimated Study Completion Date: 01 Jan 2016

Study design

Allocation: Randomized
Endpoint Classification: Bio-availability Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Basic Science

Verification:

Verified 01 Dec 2015 by Ardea Biosciences, Inc.

Sponsors

Ardea Biosciences, Inc.

Collaborators

-

Inclusion and exclusion criteria