Comparative Bioavailability - Gender Effect - Single and Multiple Ascending Dose Safety and Pharmacokinetic Study of GFT505

This study has been completed.
Sponsor:
Collaborators:
SGS Aster S.A.S.
NATURALPHA
Information provided by (Responsible Party):
Genfit
ClinicalTrials.gov Identifier:
NCT01474161
First received: November 15, 2011
Last updated: November 23, 2012
Last verified: November 2012
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study has been completed.
  Study Completion Date: November 2012
  Primary Completion Date: November 2012 (Final data collection date for primary outcome measure)