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The first‑and‑only subcutaneous T‑Cell therapy

 

 

The first‑and‑only subcutaneous T‑Cell therapy

ADVERSE REACTIONS IN THE EPCORE™ NHL-1 TRIAL

CRS-related adverse reactions were predictable, manageable, and resolvable

Predictable:

95% of CRS events occurred in the first cycle

Manageable: 

6.6% adverse event–related discontinuation

  • Discontinuation due to CRS or ICANS occurred in 1 patient each (0.6%)
  • 1 patient (0.6%) experienced a fatal adverse reaction (ICANS)

Resolvable: 

CRS resolved in 100%

  • Median duration of CRS events was 2 days (range: 0.1-27 days)

Predictable:

95% of CRS events occurred in the first cycle

Manageable: 

6.6% adverse event–related discontinuation

  • Discontinuation due to CRS or ICANS occurred in 1 patient each (0.6%)
  • 1 patient (0.6%) experienced a fatal adverse reaction (ICANS)

Resolvable: 

CRS resolved in 100%

  • Median duration of CRS events was 2 days (range: 0.1-27 days)

 

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:

  1. Tepkinly prescribing information 
  2. 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
  3. Thieblemont et al abstract LB2364, EHA 2022

 

 

IL-EPCOR-240017. Date of preparation: July 2024.