drugset / Trial / NCT01779843

Alisertib for Acute Myeloid Leukemia

NCT01779843

Phase 1 Completed 22 enrolled Massachusetts General Hospital
NaSingle-groupOpen-labelTreatment

Summary

This research study is a Phase I clinical trial. Phase I trials test the safety of an investigational drug or combination of drugs. Phase I studies also try to define the appropriate dose of the investigational drug to use for further studies. "Investigational" means that the combination of drugs is still being studied and that research doctors are trying to find out more about it. As part of this research study, you will take alisertib in combination with idarubicin and cytarabine. Alisertib has not been approved by the FDA for your cancer. However, cytarabine and idarubicin have both been approved by the FDA for treatment of AML. It also means that the FDA has not approved giving alisertib with idarubicin and cytarabine for use in patients, including patients with your type of cancer. Idarubicin and cytarabine are chemotherapy agents that are commonly used to treat individuals diagnosed with AML. Alisertib has been used in laboratory studies and those studies suggest that alisertib may slow down the spread of your cancer. It does this by blocking certain substances needed by the cancer cells to spread. In this study, researchers would like to combine alisertib with standard chemotherapy (cytarabine and idarubicin) in order to see if it can be given safely with chemotherapy in individuals with AML. The primary purpose of this research study is to determine the highest dose that alisertib can be given with idarubicin and cytarabine without severe or unmanageable side effects. The dose identified in this study will be used in future research studies.

Timeline

Start
2013-04
Primary completion
2015-11
Completion
2016-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Alisertib Small molecule 10 mg Oral
Subject Alisertib Small molecule 30 mg Oral
Background Cytarabine Small molecule 100 mg/m2 Intravenous
Background Cytarabine Small molecule 2000 mg/m2 Intravenous
Background Cytarabine Small molecule 3000 mg/m2 Intravenous
Background Idarubicin Small molecule 12 mg/m2 Intravenous