drugset / Trial / NCT00127881

Study of Human Monoclonal Antibody to Treat Mycosis Fungoides and Sezary Syndrome

NCT00127881 ↗

Phase 3 Terminated 76 enrolled Emergent Product Development Seattle LLC
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the efficacy of the drug, HuMax-CD4, in patients with mycosis fungoides(MF) and sezary syndrome who are intolerant to or do not respond to treatment with Targretin® and one other standard therapy.

Timeline

Start
2005-07
Primary completion
2014-02
Completion
—

Outcome

Outcome not reported

Stopped: “New sponsor, other treatments available”

Drugs

EvaluationDrugModalityDoseRoute
Subject Zanolimumab Monoclonal antibody — —