drugset / Trial / NCT02773732
Clinical Trial of Oral Ciprofloxacin and Etoposide in Subjects With Resistant Acute Myeloid Leukemia (AML)(UF-AML-CE-101)
Non-randomizedSequentialOpen-labelTreatment
Summary
The purpose of the first part of this study is to establish the maximum tolerated dose (MTD) of oral ciprofloxacin when given in combination with a fixed dose of oral etoposide in patients with resistant acute myeloid leukemia (AML). The purpose of the second part of this study is to determine if the established dose of oral ciprofloxacin in combination with oral etoposide is effective in the treatment of patients with resistant AML.
Timeline
- Start
- 2016-12-16
- Primary completion
- 2021-09-07
- Completion
- 2021-11-15
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ciprofloxacin | Small molecule | 500 mg | Oral |
| Subject | Ciprofloxacin | Small molecule | 750 mg | Oral |
| Subject | Ciprofloxacin | Small molecule | 1000 mg | Oral |
| Subject | Etoposide | Small molecule | 200 mg | Oral |