Myelofibrosis Clinical Trial
Official title:
A Single-arm, Single Center, Pilot Study of Siltuximab, an Anti-IL6 Therapy, for Patients With Myelofibrosis
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.
PRIMARY OBJECTIVES:
I. To evaluate safety and tolerability of the drug siltuximab in the myelofibrosis patient
population.
SECONDARY OBJECTIVES:
I. To determine clinical improvement (CI). II. To determine the overall response rate (ORR).
TERTIARY OBJECTIVES:
I. To determine if siltuximab results in improvement in iron dysregulation. II. To determine
changes in inflammatory stress that may correlate with clinical response.
OUTLINE:
Patients receive siltuximab intravenously (IV) over 60 minutes on day 1. Patients also
undergo bone marrow biopsy and aspiration at baseline and at the end of treatment (within 30
days of last siltuximab dose) or as clinically indicated. Treatment repeats every 21 days
for up to 6 courses in the absence of disease progression, unacceptable toxicity, or patient
decision to withdraw. Patients who are responding after 6 courses may receive additional
siltuximab treatment for up to 1 year at the discretion of the study doctor.
After completion of study treatment, patients are followed up at 30 days.
;
Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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