drugset / Trial / NCT01007292

A Study of YM155 Plus Rituximab in Subjects With Non-Hodgkin's Lymphoma Who Have Received Prior Treatment

NCT01007292 ↗

Phase 2 Completed 43 enrolled Astellas Pharma Inc
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate response rate, survival, safety and tolerability of YM155 given in combination with rituximab in subjects with Non-Hodgkin's Lymphoma.

Timeline

Start
2009-11
Primary completion
2013-03
Completion
2015-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Rituximab Monoclonal antibody — Intravenous
Subject SEPANTRONIUM Small molecule — Intravenous

Indications