drugset / Trial / NCT05170789

Elotuzumab, Selinexor, and Dexamethasone for Relapsed Refractory Multiple Myeloma

NCT05170789

NaSingle-groupOpen-labelTreatment

Summary

The food and drug administration (FDA) has approved the use of Selinexor, an oral, first-in class, exportin 1 (XPO1) inhibitor, in combination with low-dose dexamethasone in patients with triple-refractory (disease refractory to proteasome inhibitors (PI), immunomodulatory imid agents (IMiD), and anti-Cluster of Differentiation 38 (CD38) monoclonal antibodies (mAb)), or relapsed refractory multiple myeloma (RRMM). SLAMF7 (human Signaling Lymphocyte Activation Molecule Family 7) is a receptor that is present on immune cells, NK (Natural Killer) cells, and plasma cells. Elotuzumab, a mAb directed against the extracellular domain of SLAMF7, is used in combination with an IMiD and dexamethasone to treat RRMM. In this clinical trial, the investigators are proposing the addition of Elotuzumab to Selinexor and low-dose dexamethasone (ESd) in RRMM, previously treated with one or a combination of PI's, IMiD's, and anti-CD38 mAb.

Timeline

Start
2022-04-27
Primary completion
2022-04-27
Completion
2022-04-27

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Dexamethasone Small molecule
Subject Elotuzumab Monoclonal antibody
Subject Selinexor Other / unclassified Oral

Indications