Wednesday, July 8, 2026

Drug profile · INN

mosunetuzumab-axgb

mosunetuzumab-axgb (LUNSUMIO) is a b-lymphocyte antigen cd20 binding agent. Route of administration: injection. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 2
News articles 0
Drug details — mosunetuzumab-axgb
US status
approved
Class
Route
INJECTION
Patents
0
Programs
2
Data quality
0.84

Quick answer

mosunetuzumab-axgb (LUNSUMIO) is a b-lymphocyte antigen cd20 binding agent. Route of administration: injection. Current US regulatory status: approved.

Key facts

INN mosunetuzumab-axgb
Brand LUNSUMIO
Mechanism B-lymphocyte antigen CD20 binding agent
Target B-lymphocyte antigen CD20
Route INJECTION
Formulation INJECTABLE

Mechanism of action

B-lymphocyte antigen CD20 binding agent

Primary target: B-lymphocyte antigen CD20

Approval history

Authority Status Date
FDA approved

Pipeline programs

  1. Mosunetuzumab Phase 2 · Adaptive Biotechnologies · Diffuse Large B-Cell Lymphoma (DLBCL)
  2. Mosunetuzumab Phase 2 · Chinese Academy of · Follicular Lymphoma

Related & competitor drugs

  1. odronextamab Nervous system (NOT)
  2. ublituximab-xiiy B-lymphocyte antigen CD20 binding agent
  3. epcoritamab-bysp B-lymphocyte antigen CD20 binding agent
  4. glofitamab-gxbm B-lymphocyte antigen CD20 binding agent
  5. obinutuzumab Antineoplastic and immunomodulating agents (L01)
  6. ocrelizumab Antineoplastic and immunomodulating agents (L04)

Frequently asked questions

What is mosunetuzumab-axgb?

mosunetuzumab-axgb (LUNSUMIO) is a b-lymphocyte antigen cd20 binding agent. Route of administration: injection. Current US regulatory status: approved.

What is the brand name for mosunetuzumab-axgb?

LUNSUMIO is a marketed brand name for mosunetuzumab-axgb. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of mosunetuzumab-axgb?

mosunetuzumab-axgb has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.