A Study of Ribavirin to Treat M4 and M5 Acute Myelocytic Leukemia

Phase 2

Completed

• Conditions: Acute Myelocytic Leukemia
• Interventions: Drug: ribavirin

• Registration Number: NCT00559091
• Lead Sponsor: Jewish General Hospital

Brief Summary

The purpose of this study is to determine if ribavirin (a drug commonly used to treat hepatitis C) also has activity in the treatment of patients with refractory or relapsed acute myeloid leukemia (AML) of the M4 and M5 subtype.

Detailed Description

The eukaryotic translation initiation factor eIF4E is dysregulated in many human malignancies, including a subset of myeloid leukemia (M4/M5 AML and blast crisis CML). eIF4E overexpression leads to oncogenic transformation. Ribavirin impedes eIF4E mediated transformation in vitro, in primary human specimens and in animal models.

While ribavirin has been used extensively for the treatment of viral hepatitis C and its safety profile has been well defined, it has never been used in patients with AML. This study will establish the efficacy and safety of ribavirin in M4/M5 AML patients. In addition, this study will also include correlative studies to determine the effect of ribavirin on eIF4E activity and eIF4E related pathways in M4/M5 AML patients.

Study Timeline

• Study Start: 2007-04
• Study First Submitted: 2007-11-15
• Study First Submitted QC: 2007-11-15
• Study First Posted: 2007-11-16
• Primary Completion: 2010-02
• Study Completion: 2010-02
• Status Verified: 2022-12
• Last Update Submitted: 2022-12-20
• Last Update Posted: 2022-12-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 18

Inclusion Criteria

• A diagnosis of acute myeloid leukemia (AML), either M4 or M5 subtype de novo or resulting from a transformation from MDS or a myeloproliferative disorder.
• Patients with AML who (a) have failed primary therapy -defined as failing two induction chemotherapies, (b) have relapsed or (c) are not suitable for intensive induction chemotherapy will be eligible. OR
• Patients with AML blast crisis from CML if they are not suitable candidates for intensive induction chemotherapy or have failed imatinib mesylate OR
• Patients with secondary AML after MDS if they are not suitable candidates for intensive induction chemotherapy.
• ECOG 0,1,2, or 3
• Life expectancy > 12 weeks.
• Adequate renal and hepatic function

Exclusion Criteria

• Uncontrolled central nervous system involvement by AML
• Active cardiovascular disease as defined by NYHA class III-IV categorization.
• Intercurrent illness or medical condition precluding safe administration of ribavirin.
• Received any previous therapy within 28 days prior to study entry.Hydrea is permitted but must be stopped 7 days prior to starting study drug.
• Known infection with HIV.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
I	ribavirin	Ribavirin

Primary Outcome Measures

Name	Time	Method
Measure: Overall response rate	6 months

Secondary Outcome Measures

Name	Time	Method
Measure: Safety and tolerability, correlative studies	6 months

Trial Locations

Locations (3)

Maisonneuve-Rosemont Hospital; 🇨🇦 Montreal, Quebec, Canada

McMaster Hospital; 🇨🇦 Hamilton, Ontario, Canada

Jewish General Hospital; 🇨🇦 Montreal, Quebec, Canada