drugset / Trial / NCT02013804

A Phase 1 Multicenter Open-label Study to Evaluate the Safety Tolerability and PK of MEDI0680 (AMP-514) in Subjects With Advanced Malignancies

NCT02013804

Phase 1 Completed 58 enrolled MedImmune LLC
NaSingle-groupOpen-labelTreatment

Summary

This is a multicenter, open label, first-in-human dose-escalation study of MEDI0680 (AMP-514) to evaluate the safety, tolerability, PK, immunogenicity (IM), and antitumor activity in adult subjects with solid tumors.

Timeline

Start
2013-12-19
Primary completion
2017-05-18
Completion
2017-05-18

Drugs

EvaluationDrugModalityDoseRoute
Subject MEDI0680 Monoclonal antibody 0.1 mg/kg Intravenous
Subject MEDI0680 Monoclonal antibody 0.5 mg/kg Intravenous
Subject MEDI0680 Monoclonal antibody 2.5 mg/kg Intravenous
Subject MEDI0680 Monoclonal antibody 10 mg/kg Intravenous
Subject MEDI0680 Monoclonal antibody 20 mg/kg Intravenous

Indications