drugset / Trial / NCT03587844

Dosing of Brentuximab Vedotin for Mycosis Fungoides, Sezary Syndrome Patients

NCT03587844

Non-randomizedSequentialOpen-labelTreatment

Summary

The purpose of this study is to test any good and bad effects of the study drug called brentuximab vedotin at a lower dose than is FDA-approved.

Timeline

Start
2018-07-03
Primary completion
2027-07
Completion
2027-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Brentuximab Vedotin Monoclonal antibody 0.9 mg/kg Intravenous
Subject Brentuximab Vedotin Monoclonal antibody 1.2 mg/kg Intravenous