Regeneron makes Libtayo and has a large portfolio of CD3 bispecifics (odronextamab, linvoseltamab).
Regeneron, based in Tarrytown, New York, and listed as REGN, makes Libtayo, or cemiplimab, and has a large portfolio of CD3 bispecific antibodies including odronextamab and linvoseltamab. Odronextamab targets CD20 by CD3 in lymphoma, linvoseltamab, a BCMA by CD3 bispecific, was approved in 2025 for myeloma, fianlimab is a LAG-3 antibody in a phase 3 with cemiplimab in first-line melanoma, and costimulatory bispecifics follow. OnCo links it to cutaneous squamous cell carcinoma, basal cell carcinoma and cervical cancer through the EMPOWER-Cervical 1 trial, to lymphoma pages, to MUC16 as a target and to Arsenal Biosciences. Whether costimulatory bispecifics can make T-cell engagers work in solid tumours is the open question its pipeline is built to answer. Cemiplimab has its own page.
A PD-1 blocker that is the standard for advanced skin squamous cell carcinoma, and in 2025 became the first adjuvant immunotherapy for it.
Fianlimab is Regeneron's LAG-3 blocking antibody, paired with the PD-1 blocker cemiplimab. A 60% phase 1 response rate in untreated melanoma prompted phase 3 trials, but the metastatic trial against pembrolizumab missed its progression endpoint in 2026.
Linvoseltamab is Regeneron's BCMA bispecific, approved in July 2025 with the highest complete-response rate of the class in its pivotal study.
Odronextamab is Regeneron's CD20 bispecific, approved in Europe for lymphoma and in the US for follicular lymphoma after earlier FDA rejections over confirmatory-trial enrolment.
REGN7075 is a bispecific antibody from Regeneron Pharmaceuticals, in registered phase 2 trials for non-small-cell lung cancer, small-cell lung cancer.
Ubamatamab (REGN4018) is Regeneron's investigational MUC16×CD3 bispecific antibody, in phase 1/2 and phase 2 trials for ovarian and endometrial cancer.
Ziv-aflibercept (Zaltrap) is a decoy receptor that soaks up the blood-vessel growth signal VEGF. It is added to the FOLFIRI chemotherapy combination for bowel cancer that has spread and progressed after oxaliplatin.
Shares A Window of Opportunity Trial to Learn if Linvoseltamab is Safe and Well Tolerated, and How Well it Works in Adult Participants With Recently Diagnose, A Proof-of-Concept Study to Learn Whether Linvoseltamab Can Eliminate Abnormal Plasma Cells That May Lead to Multiple Myeloma in Adult Patients With H, A Proof-of-Concept Trial to Study the Safety and Activity of Linvoseltamab in Adult Participants With Smoldering Multiple Myeloma at High Risk of Deve, A Study to Assess the Safety and Anti-Tumor Activity of REGN7945 in Combination With Linvoseltamab in Adult Participants With Relapsed/Refractory Mult.
Shares EMPOWER-Cervical 1 / GOG-3016 / ENGOT-cx9, Ziv-aflibercept, Neoadjuvant cemiplimab for resectable stage II to IV skin squamous cell carcinoma, Cemiplimab in basal cell carcinoma after a hedgehog inhibitor.
Shares Study of Intralesional Cemiplimab in Adult Patients With Early Stage Cutaneous Squamous Cell Carcinoma, Cemiplimab for kidney transplant recipients with advanced skin squamous cell carcinoma, Neoadjuvant cemiplimab for resectable stage II to IV skin squamous cell carcinoma, C-POST (cemiplimab after surgery and radiotherapy for high-risk skin squamous cell carcinoma).
Shares A Proof-of-Concept Study to Learn Whether Linvoseltamab Can Eliminate Abnormal Plasma Cells That May Lead to Multiple Myeloma in Adult Patients With H, A Proof-of-Concept Trial to Study the Safety and Activity of Linvoseltamab in Adult Participants With Smoldering Multiple Myeloma at High Risk of Deve, A Study to Compare Linvoseltamab and Daratumumab Treatment in High-Risk Smoldering Multiple Myeloma (HR-SMM), Linvoseltamab.
Shares Ubamatamab, A Study to Assess the Anti-Tumor Activity and Safety of Odronextamab in Adult Patients With B-cell Non-Hodgkin Lymphoma Who Have Been Previously Treat, Safety and efficacy of odronextamab in patients with relapsed or refractory follicular lymphoma, Linvoseltamab.