drugset / Trial / NCT02840721

Safety, Efficacy, and Tolerability Study of PF-06480605 in Subjects With Moderate to Severe Ulcerative Colitis.

NCT02840721

Phase 2 Completed 50 enrolled Telavant, Inc. Pfizer · collab
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, and efficacy of PF-06480605 in subjects with moderate to severe ulcerative colitis.

Timeline

Start
2016-10-26
Primary completion
2018-05-31
Completion
2018-08-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Afimkibart Monoclonal antibody 500 mg Intravenous

Indications