Overview

Assessment of AMG 420 in Subjects With Relapsed and/or Refractory Multiple Myeloma

Status:
Active, not recruiting
Trial end date:
2022-06-29
Target enrollment:
Participant gender:
Summary
To confirm the maximum tolerated dose (MTD) from the BI 836909 trial of 400 mcg/d, given as 28-day continuous intravenous infusion in patients with relapsed and/or refractory multiple myeloma, to test the 600 mcg/d dose, given as a 28-day continuous iV infusion.
Phase:
Phase 1
Details
Lead Sponsor:
Amgen