drugset / Trial / NCT00375453

Dose Escalation Study of SH U04722 in Solid Tumors

NCT00375453 ↗

Phase 1 Terminated 10 enrolled Bayer
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study will evaluate the safety and tolerability of SH U04722 in patients with solid tumor cancers. In addition, this study will identify the recommended dose and administration schedule of SH U04722 for phase II development in Japanese cancer patients, evaluate the pharmacokinetic profile of SH U04722 and gather preliminary data on the effectiveness of SH U04722 in patients with solid tumors.

Timeline

Start
2007-01
Primary completion
2007-10
Completion
2007-10

Drugs

EvaluationDrugModalityDoseRoute
Subject SH U04722 Unknown — —

Indications