Odronextamab is a hinge-stabilized, fully human immunoglobulin G4 (IgG4)-based CD20×CD3 bispecific antibody currently evaluated for the treatment of relapsed/refractory (R/R) B-Cell non-Hodgkin lymphoma (NHL). Preliminary studies have shown that in patients with R/R NHL, the use of odronextamab does not lead to the development of neurologic toxicity; however, it can lead to the development of cytokine release syndrome (CRS), a serious condition associated with the use of immunotherapy. In December 2020, the FDA placed a partial clinical hold and requested the drug developer, Regeneron Pharmaceuticals, to amend clinical protocols to reduce the incidence of CRS. The partial clinical hold was later lifted in May 2021.
A phase I clinical study (NCT02290951) showed that in heavily pre-treated patients with B-cell non-Hodgkin lymphoma, odronextamab elicited a durable response with a manageable safety profile.
Liverpool Hospital, Liverpool, New South Wales, Australia
Zonguldak Bulent Ecevit Univesity, Zonguldak, Turkey
Princess Alexandra Hospital, Woolloongabba, Queensland, Australia
The Hillingdon Hospitals NHS Foundation Trust, Uxbridge, London, United Kingdom
Investigative Clinical Research of Indiana, Noblesville, Indiana, United States
University of Kentucky, Lexington, Kentucky, United States
City of Hope, Duarte, California, United States
Norton Cancer Institute, Louisville, Kentucky, United States
Massachusetts General Hospital, Boston, Massachusetts, United States
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