drugset / Trial / NCT02318394

A Phase 1 Study of MEDI0562 in Adult Subjects With Selected Advanced Solid Tumors

NCT02318394

Phase 1 Completed 56 enrolled MedImmune LLC
NaSingle-groupOpen-labelTreatment

Summary

To evaluate the safety and tolerability of MEDI0562 in adult subjects with selected advanced solid tumors

Timeline

Start
2015-03-02
Primary completion
2018-01-09
Completion
2018-01-09

Drugs

EvaluationDrugModalityDoseRoute
Subject TAVOLIMAB Monoclonal antibody 0.03 mg/kg Intravenous
Subject TAVOLIMAB Monoclonal antibody 0.1 mg/kg Intravenous
Subject TAVOLIMAB Monoclonal antibody 0.3 mg/kg Intravenous
Subject TAVOLIMAB Monoclonal antibody 1 mg/kg Intravenous
Subject TAVOLIMAB Monoclonal antibody 3 mg/kg Intravenous
Subject TAVOLIMAB Monoclonal antibody 10 mg/kg Intravenous

Indications