drugset / Trial / NCT03145181

Dose Escalation Study of Teclistamab, a Humanized BCMA*CD3 Bispecific Antibody, in Participants With Relapsed or Refractory Multiple Myeloma

NCT03145181

Phase 1 Active not recruiting 302 enrolled Janssen Research & Development, LLC
Non-randomizedSequentialOpen-labelTreatment

Summary

The purpose of this study is to identify the recommended Phase 2 dose(s) (RP2Ds) and schedule assessed to be safe for Teclistamab and to characterize the safety and tolerability of Teclistamab at the RP2Ds.

Timeline

Start
2017-05-16
Primary completion
2025-09-25
Completion
2027-05-28

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Teclistamab Monoclonal antibody 0.27 mg/kg Intravenous
Subject Teclistamab Monoclonal antibody 0.72 mg/kg Intravenous
Subject Teclistamab Monoclonal antibody 1.5 mg/kg Intravenous