Friday, July 10, 2026

Drug profile · INN

linvoseltamab

linvoseltamab (LYNOZYFIC) is an FDA-listed pharmaceutical active ingredient. Associated with Regeneron UK Limited.

EMA: approved Antineoplastic and immunomodulating agents (L01) L01FX
Patents linked 0
Pipeline programs 16
News articles 4
Drug details — linvoseltamab

Quick answer

linvoseltamab (LYNOZYFIC) is an FDA-listed pharmaceutical active ingredient. Associated with Regeneron UK Limited.

Key facts

INN linvoseltamab
Brand LYNOZYFIC
Therapeutic class Antineoplastic and immunomodulating agents (L01)
ATC code L01FX

Approval history

Authority Status Date
EMA approved

Recent coverage

Pipeline programs

  1. Linvoseltamab Phase 3 · Regeneron UK · High Risk Smoldering Multiple Myeloma (HR-SMM)
  2. Linvoseltamab Phase 3 · Regeneron UK · Relapsed Refractory Multiple Myeloma (RRMM)
  3. Linvoseltamab Phase 3 · Regeneron UK · Relapsed and/or Refractory Multiple Myeloma (RRMM)
  4. Linvoseltamab Phase 3 · Regeneron UK · Multiple Myeloma (MM)
  5. Linvoseltamab Phase 3 · Regeneron UK · Multiple Myeloma
  6. Linvoseltamab Phase 2 · Regeneron UK · Smoldering Multiple Myeloma (SMM)
  7. Linvoseltamab Phase 2 · Regeneron UK · Monoclonal Gammopathy of Undetermined Significance (MGUS)
  8. Linvoseltamab Phase 2 · Regeneron UK · Recurrent Multiple Myeloma

Related & competitor drugs

  1. abiraterone acetate Antineoplastic and immunomodulating agents (L02)
  2. anagrelide Antineoplastic and immunomodulating agents (L01)
  3. apremilast Antineoplastic and immunomodulating agents (L04)
  4. arsenic trioxide Antineoplastic and immunomodulating agents (L01)
  5. axitinib Antineoplastic and immunomodulating agents (L01)
  6. azacitidine Antineoplastic and immunomodulating agents (L01)

Frequently asked questions

What is linvoseltamab?

linvoseltamab (LYNOZYFIC) is an FDA-listed pharmaceutical active ingredient. Associated with Regeneron UK Limited.

What is the brand name for linvoseltamab?

LYNOZYFIC is a marketed brand name for linvoseltamab. Check FDA Drugs@FDA for the current US label holder and prescribing information.