2024
P-057 Comparative Efficacy of Cilta-Cel vs Approved Comparator Treatments for Patients With Relapsed/Refractory Multiple Myeloma With 1–3 Prior Lines of Therapy: A Network Meta-Analysis
Mina R, Khan A, McClune B, Bar N, Caers J, Larsen J, Mendes J, Lee S, Benachour N, Chen D, Zhao M, Lonardi C, Slaughter A, Lengil T, Burnett H, Cichewicz A, Neupane B, Filho O, Dytfeld D, Sidana S. P-057 Comparative Efficacy of Cilta-Cel vs Approved Comparator Treatments for Patients With Relapsed/Refractory Multiple Myeloma With 1–3 Prior Lines of Therapy: A Network Meta-Analysis. Clinical Lymphoma Myeloma & Leukemia 2024, 24: s74. DOI: 10.1016/s2152-2650(24)01960-8.Peer-Reviewed Original Research
2023
Alnuctamab (ALNUC; BMS-986349; CC-93269), a 2+1 B-Cell Maturation Antigen (BCMA) × CD3 T-Cell Engager (TCE), Administered Subcutaneously (SC) in Patients (Pts) with Relapsed/Refractory Multiple Myeloma (RRMM): Updated Results from a Phase 1 First-in-Human Clinical Study
Bar N, Mateos M, Ribas P, Hansson M, Paris L, Hofmeister C, Otero P, Bermúdez M, Martin T, Santoro A, Yee A, Creignou M, Rodriguez C, Cerchione C, De La Rubia J, Oriol A, Waibel H, Besemer B, Thompson E, Kiesel B, Chen J, Chung A, Boss I, Gaudy A, Li S, Hsu K, Godwin C, Burgess M, San-Miguel J, Costa L. Alnuctamab (ALNUC; BMS-986349; CC-93269), a 2+1 B-Cell Maturation Antigen (BCMA) × CD3 T-Cell Engager (TCE), Administered Subcutaneously (SC) in Patients (Pts) with Relapsed/Refractory Multiple Myeloma (RRMM): Updated Results from a Phase 1 First-in-Human Clinical Study. Blood 2023, 142: 2011. DOI: 10.1182/blood-2023-180013.Peer-Reviewed Original ResearchRelapsed/Refractory Multiple MyelomaTreatment-emergent adverse eventsT-cell engagersLines of therapyOverall response ratePhase 1 studyTarget dosesTarget doseMedian PFSData cutoffMedian timeSafety profileCD3 T-cell engagerUpper respiratory tract infectionAnti-CD38 therapyAntitumor activityGrade 1 neurotoxicityTreatment-related deathsCytokine release syndromeRefractory multiple myelomaRespiratory tract infectionsPhase 1 trialPopulation pharmacokinetic analysisHuman clinical studiesObserved trough concentrations