ADVERSE REACTIONS IN THE EPCORE™ NHL-1 TRIAL
CRS-related adverse reactions were predictable, manageable, and resolvable
Manageable safety profile
Only 6.6% of patients discontinued subcutaneous TEPKINLY due to adverse reactions.
Patient experienced ICANS after intermediate dose with multiple confounders, including extensive opioid use for Gr3 pancreatitis, hyperammonemia, multifocal cerebral infarcts in setting of possible microangiopathy, and tocilizumab administration3
Download the Dosing and Administration Guide for more information on how TEPKINLY is administered.
References:
- Tepkinly prescribing information
- Thieblemont C, Phillips T, Ghesquieres H, et al. Epcoritamab, a novel, subcutaneous CD3xCD20 bispecific T-cell-engaging antibody, in relapsed or refractory large B-cell lymphoma: dose expansion in a phase I/II trial. J Clin Oncol. 2023;41(12):2238-2247. doi:10.1200/JCO.22.01725
- Thieblemont et al abstract LB2364, EHA 2022
IL-EPCOR-240017. Date of preparation: July 2024.