drugset / Trial / NCT03523390

Phase I/Ib Multiple Ascending Dose Study in China

NCT03523390

Phase 1 Completed 24 enrolled Merck KGaA, Darmstadt, Germany
Non-randomizedSequentialOpen-labelTreatment

Summary

The purpose of this study was to evaluate the maximum tolerated dose (MTD) and pharmacokinetics (PK) of Avelumab monotherapy in Chinese subjects.

Timeline

Start
2018-04-24
Primary completion
2019-07-29
Completion
2021-02-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Avelumab Monoclonal antibody 3 mg/kg Intravenous
Subject Avelumab Monoclonal antibody 10 mg/kg Intravenous
Subject Avelumab Monoclonal antibody 20 mg/kg Intravenous

Indications