drugset / Trial / NCT06225310

A Trial of Selinexor, Ruxolitinib and Methylprednisolone

NCT06225310

Phase 1 Recruiting 30 enrolled Oncotherapeutics
NaSingle-groupOpen-labelTreatment

Summary

Selinexor, a first-in-class, oral selective exportin 1 (XPO1) inhibitor, has shown promise in pre-clinical and clinical studies. It functions by inhibiting the nuclear export protein XPO1, resulting in the accumulation of tumor suppressor proteins and inhibition of oncoprotein mRNAs, which is selectively lethal to myeloma cells. Selinexor has demonstrated activity in combination with various drugs, including glucocorticoids and proteasome inhibitors, leading to its FDA approval for the treatment of relapsed or refractory multiple myeloma.

Timeline

Start
2024-08-06
Primary completion
2027-04-01
Completion
2027-05-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Ruxolitinib Small molecule 10 mg Oral
Subject Ruxolitinib Small molecule 15 mg Oral
Subject Selinexor Other / unclassified 40 mg Oral
Subject Selinexor Other / unclassified 60 mg Oral
Background Methylprednisolone Other / unclassified 40 mg Oral

Indications