Overview

A Pilot Study of FFP104 in Subjects With Crohn's Disease

Status:
Unknown status
Trial end date:
2017-12-01
Target enrollment:
Participant gender:
Summary
This study will be conducted to evaluate the safety, tolerability and efficacy of intravenously administered FFP104 or placebo over 15 days (3 total doses) in subjects with moderate to severely active Crohn's Disease
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
Fast Forward Pharmaceuticals