drugset / Trial / NCT00061620

Phase I Study of Continuous Infusion Schedule of FMdC in Hematologic Malignancies

NCT00061620 ↗

Non-randomizedSingle-groupOpen-labelTreatment

Summary

The goal of this clinical research study is to find the highest dose of Tezacitabine (FMdC) which can be safely given as a continuous infusion by vein to patients with hematologic malignancies. The general safety and effectiveness of this drug will also be studied.

Timeline

Start
2001-09-06
Primary completion
2004-02-12
Completion
2004-02-12

Drugs

EvaluationDrugModalityDoseRoute
Subject TEZACITABINE ANHYDROUS Other / unclassified 7.5 mg/m2 Intravenous