drugset / Trial / NCT00412789

Efficacy and Safety of Patupilone in Patients With Advanced Solid Tumors in Japan

NCT00412789 ↗

Phase 1 Completed 15 enrolled Novartis Pharmaceuticals
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The study will evaluate the safety and efficacy of Patupilone in adult patients with advanced solid tumors.

Timeline

Start
2006-08
Primary completion
2008-01
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject Patupilone Small molecule — Intravenous

Indications