drugset / Trial / NCT02465944

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

NCT02465944 ↗

Phase 1/2 Unknown 24 enrolled Fast Forward Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

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

Timeline

Start
2016-01
Primary completion
2017-08
Completion
2017-12

Drugs

EvaluationDrugModalityDoseRoute
Subject FFP104 Monoclonal antibody 2.5 mg/kg Intravenous
Subject FFP104 Monoclonal antibody 5 mg/kg Intravenous

Indications