drugset / Trial / NCT00381173

A Study of ZYC300 Administered With Cyclophosphamide Pre-Dosing

NCT00381173 ↗

Phase 1 Completed 22 enrolled Eisai Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the feasibility, safety, and tolerability of administering ZYC300 with Cyclophosphamide (Cytoxan).

Timeline

Start
2006-11
Primary completion
2008-10
Completion
2008-10

Drugs

EvaluationDrugModalityDoseRoute
Subject ZYC300 Unknown 400 ug —
Background Cyclophosphamide Other / unclassified 600 mg/m2 Intravenous