drugset / Trial / NCT05556616

A Study of Modakafusp Alfa in Adult Participants With Multiple Myeloma

NCT05556616

Phase 1 Terminated 15 enrolled Teva Branded Pharmaceutical Products R&D, Inc.
RandomizedSequentialOpen-labelTreatment

Summary

The main aims of this study are to test for any side effects from modakafusp alfa in combination therapy and to determine the recommended dose of combination therapy with modakafusp alfa. The dose of modakafusp alfa will be increased a little at a time until the highest dose that does not cause harmful side effects is found. Participants will be given modakafusp alfa through a vein.

Timeline

Start
2023-01-12
Primary completion
2024-06-04
Completion
2024-06-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Bortezomib Small molecule Subcutaneous
Subject Carfilzomib Other / unclassified 70 mg/m2 Intravenous
Subject Daratumumab Monoclonal antibody Subcutaneous
Subject Lenalidomide Other / unclassified 10 mg Oral
Subject Modakafusp alfa Protein / enzyme biologic 80 mg Intravenous
Subject Pomalidomide Other / unclassified 2 mg Oral
Subject Pomalidomide Other / unclassified 4 mg Oral

Indications