drugset / Trial / NCT03144245

Study of AMV564 in Patients With AML

NCT03144245 ↗

Phase 1 Completed 53 enrolled Amphivena Therapeutics, Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This is a first in human, non randomized, open-label, dose escalation study to investigate the safety, tolerability and preliminary efficacy of AMV564.

Timeline

Start
2017-03-20
Primary completion
2020-07-21
Completion
2020-11-05

Drugs

EvaluationDrugModalityDoseRoute
Subject AMV564 Protein / enzyme biologic — Intravenous
Subject Pembrolizumab Monoclonal antibody — Intravenous