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Clinical Trial Summary

This is a Phase 1/2, multicenter, open-label study to evaluate the efficacy, and safety of various combinations with selinexor in participants with RR DLBCL. The study will be conducted in two phases: Phase 1 and 2. The Phase 1 of the study will be a standard 3 + 3 dose escalation to determine the maximal tolerated dose (MTD), recommended Phase 2 dose (RP2D) for each treatment arm, and assess the dose limiting toxicities (DLTs). The Phase 2 of the study will be a dose expansion study to assess the efficacy and safety of for RP2D selected at the end of Phase 1 of the study for each treatment arm.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04607772
Study type Interventional
Source Karyopharm Therapeutics Inc
Contact
Status Suspended
Phase Phase 1/Phase 2
Start date November 18, 2020
Completion date December 2025

See also
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