drugset / Trial / NCT06232707

A Study to Evaluate Efficacy and Safety of Alnuctamab Compared to Standard of Care Regimens in Participants With Relapsed or Refractory Multiple Myeloma (RRMM)

NCT06232707 ↗

Phase 3 Withdrawn Celgene Corporation
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of alnuctamab compared to standard of care regimens in participants with relapsed or refractory multiple myeloma (RRMM).

Timeline

Start
2024-05-03
Primary completion
2025-11-16
Completion
2030-09-21

Outcome

Outcome not reported

Stopped (Business): “Business objectives have changed”

Drugs

EvaluationDrugModalityDoseRoute
Subject Alnuctamab Protein / enzyme biologic — —
Comparator Carfilzomib Other / unclassified — —
Comparator Daratumumab Monoclonal antibody — —
Comparator Dexamethasone Small molecule — —
Comparator Elotuzumab Monoclonal antibody — —
Comparator Pomalidomide Other / unclassified — —

Indications