drugset / Trial / NCT02696642

Phase I Study of Anetumab Ravtansine in Hepatic or Renal Impairment

NCT02696642

Phase 1 Completed 54 enrolled Bayer
Non-randomizedParallel-groupOpen-labelTreatment

Summary

To characterize the safety, tolerability, pharmacokinetics and immunogenicity of anetumab ravtansine in subjects with advanced solid cancers and with different degrees of hepatic or renal impairment

Timeline

Start
2016-04-14
Primary completion
2018-07-31
Completion
2019-08-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Anetumab Ravtansine Monoclonal antibody 6.5 mg/kg Intravenous

Indications