drugset / Trial / NCT00861874
A Study of Decitabine in Combination With Escalating Doses of Rapamycin in Patients With Relapsed or Refractory Acute Myeloid Leukemia
Non-randomizedSingle-groupOpen-labelTreatment
Summary
The purpose of this study is to determine the safety and feasibility of the combination of decitabine given at a fixed dose with escalating doses of rapamycin in patients with relapsed or refractory acute myeloid leukemia.
Timeline
- Start
- 2010-01
- Primary completion
- 2012-09
- Completion
- —
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Decitabine | Small molecule | 20 mg/m2 | Intravenous |
| Subject | Sirolimus | Small molecule | 2 mg | Oral |
| Subject | Sirolimus | Small molecule | 4 mg | Oral |
| Subject | Sirolimus | Small molecule | 6 mg | Oral |