drugset / Trial / NCT04883957

Study of BGB-11417 in Adult Participants With Mature B-cell Malignancies

NCT04883957

Phase 1 Active not recruiting 64 enrolled BeiGene
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of BGB-11417 monotherapy, define the maximum tolerated dose (MTD) or maximum administered dose and the recommended Phase 2 dose (RP2D) of BGB-11417 monotherapy for the selected B-cell malignancy dose finding cohorts, and evaluate the safety and tolerability of the ramp-up dosing schedule in the evaluated disease types.

Timeline

Start
2021-07-05
Primary completion
2026-08-31
Completion
2026-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Sonrotoclax Other / unclassified Oral