Genmab A/S (Nasdaq: GMAB) today announced the results from multiple clinical trials evaluating epcoritamab (DuoBody®-CD3xCD20), an investigational subcutaneous bispecific antibody, alone or in combination with other therapies for the treatment of patients with relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL
Epcoritamab BLA accepted for FDA Priority review; FDA action date is May 21, 2023
Epcoritamab could become the first subcutaneous bispecific antibody approved for the treatment of LBCL
BLA submission supported by
Epcoritamab BLA accepted for FDA Priority review; FDA action date is May 21, 2023