drugset / Trial / NCT03340883

Safety and Tolerability of BION-1301 in Adults With Relapsed or Refractory Multiple Myeloma (MM)

NCT03340883

Phase 1/2 Terminated 21 enrolled Chinook Therapeutics, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a Phase 1/2 study designed to evaluate the safety and tolerability of BION-1301 in adults with relapsed or refractory multiple myeloma whose disease has progressed after 3 or more prior systemic therapies.

Timeline

Start
2017-11-15
Primary completion
2019-06-13
Completion
2019-07-09

Drugs

EvaluationDrugModalityDoseRoute
Subject zigakibart Monoclonal antibody

Indications