Stopped: A business decision was made to discontinue further enrollment. There were no safety concerns that contributed to this decision.
The purpose of this single-arm, open-label, Phase 1b/2a, multicenter basket study is to evaluate whether tafasitamab and parsaclisib can be safely combined at the recommended Phase 2 dose (RP2D) and dosing regimen that was established for each of the 2 compounds as a treatment option for adult participants with R/R B-cell malignancies.
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Number of Participants With Any Treatment-emergent Adverse Event (TEAE )
Timeframe: up to 1092 days
Number of Participants With Any ≥Grade 3 TEAE
Timeframe: up to 1092 days
Number of Participants With Dose-limiting Toxicities (DLTs)
Timeframe: up to 28 days
Objective Response Rate Based on Investigator Assessment: Percentage of Participants With CR/CMR or PR/PMR According to Lugano Criteria for NHL and International Working Group for Chronic Lymphocytic Leukemia (iwCLL) Criteria for CLL
Timeframe: up to 1002 days