A Study of Pembrolizumab Added to the Standard First-Line Therapy of Cyclophosphamide, Bortezomib, and Dexamethasone (CyBorD) for NDMM NTE

PHASE2WithdrawnINTERVENTIONAL
0
Timeline

Start Date

February 17, 2021

Primary Completion Date

October 31, 2022

Study Completion Date

October 31, 2022

Conditions
Multiple Myeloma
Interventions
DRUG

Pembrolizumab

Patients not progressing after 2 cycles of CyBorD treatment and achieving less than VGPR by IMWG criteria will be screened to receive pembrolizumab intravenously at 200mg at day 1 of every 3-week cycle for 8 cycles (24 weeks) starting Cycle 4 of CyBorD. CyBorD will be discontinued after 24 weeks and pembrolizumab will be administered as a single agent at the same dose for an additional 27 cycles (81 weeks).

Trial Locations (4)

R3E0V9

CancerCare Manitoba, Winnipeg

E1C6Z8

The Moncton Hospital, Moncton

J1H5N4

CIUSSS de l'Estrie-CHUS, Sherbrooke

S4T7T1

Allan Blair Cancer Centre, Regina

All Listed Sponsors
collaborator

Merck Sharp & Dohme LLC

INDUSTRY

lead

Canadian Myeloma Research Group

OTHER

NCT04258683 - A Study of Pembrolizumab Added to the Standard First-Line Therapy of Cyclophosphamide, Bortezomib, and Dexamethasone (CyBorD) for NDMM NTE | Biotech Hunter | Biotech Hunter