drugset / Trial / NCT01214642

A Dose-Escalation Study for Patients With Advanced Cancer

NCT01214642

Phase 1 Completed 63 enrolled Eli Lilly and Company
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study is being conducted to determine the safety of LY2523355 for the treatment of advanced and/or metastatic cancer (including Non-Hodgkin's lymphoma).

Timeline

Start
2008-05
Primary completion
2011-12
Completion
2012-06

Drugs

EvaluationDrugModalityDoseRoute
Subject litronesib Small molecule 2 mg/m2 Intravenous
Subject litronesib Small molecule 8 mg/m2 Intravenous
Subject litronesib Small molecule 12 mg/m2 Intravenous
Background Pegfilgrastim Protein / enzyme biologic 6 mg Subcutaneous

Indications

No indication recorded.