Clinical Trials Directory

Trials / Completed

CompletedNCT01246622

Lenalidomide and Cytarabine in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia

Phase I Trial of Cytarabine and Lenalidomide in Relapsed or Refractory Acute Myeloid Leukemia Patients

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
32 (actual)
Sponsor
Roswell Park Cancer Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This phase I trial is studying the side effects and best dose of lenalidomide when given together with cytarabine in treating patients with relapsed or refractory acute myeloid leukemia (AML). Biological therapies, such as lenalidomide, may stimulate the immune system in different ways and stop cancer cells from growing. Drugs used in chemotherapy, such as cytarabine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving lenalidomide together with cytarabine may kill more cancer cells

Detailed description

PRIMARY OBJECTIVES: I. Determine the maximum tolerated dose (MTD) of lenalidomide following intermediate dose ARA-C (cytarabine) in relapsed/refractory AML. SECONDARY OBJECTIVES: I. Evaluate immune reconstitution in patients in complete remission (CR) treated at the MTD. II. Evaluate the efficacy of the regimen in the expanded group treated at the MTD. OUTLINE: This is a dose-escalation study of lenalidomide. Patients receive lenalidomide orally (PO) on days 6-26 and cytarabine intravenously (IV) over 3 hours on days 1-5. Treatment repeats every 28 days for up to 2 courses in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up at 2 weeks and then every 3 months thereafter.

Conditions

Interventions

TypeNameDescription
DRUGcytarabineGiven IV
DRUGlenalidomideGiven PO

Timeline

Start date
2011-02-07
Primary completion
2014-05-15
Completion
2019-06-05
First posted
2010-11-23
Last updated
2020-09-24

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01246622. Inclusion in this directory is not an endorsement.