drugset / Trial / NCT02805868

Siltuximab in Treating Patients With Primary, Post-Polycythemia Vera, or Post-Essential Thrombocythemia Myelofibrosis

NCT02805868

NaSingle-groupOpen-labelTreatment

Summary

The main purpose of this investigational research study is to determine how safe and tolerable the study drug siltuximab is in patients with myelofibrosis (MF). This medication has been approved by the FDA for another condition (multicentric castleman's disease (MCD), but not for myelofibrosis (MF). In MCD, siltuximab resulted in improvement in symptoms and anemia. While MCD and MF are different diseases, they share some common features including a protein call interleukin-6 (IL-6) that may be important in causing symptoms of MCD and MF.

Timeline

Start
2016-06
Primary completion
2019-02
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Siltuximab Monoclonal antibody Intravenous