drugset / Trial / NCT00866970

Safety, Efficacy and Pharmacokinetics of ALD518 in Patients With Non-Small Cell Lung Cancer-related Fatigue and Cachexia

NCT00866970

Phase 2 Completed 124 enrolled CSL Behring
RandomizedSingle-groupQuadruple-blindTreatment

Summary

The purpose of this study is to asses the safety and efficacy of ALD518 in patients with Non-Small Cell Lung Cancer-Related Fatigue and cachexia (weight-loss).

Timeline

Start
2008-09
Primary completion
2009-08
Completion
2009-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Clazakizumab Monoclonal antibody 80 mg Intravenous
Subject Clazakizumab Monoclonal antibody 160 mg Intravenous
Subject Clazakizumab Monoclonal antibody 360 mg Intravenous