Friday, July 10, 2026

Drug profile · INN

rituximab

rituximab (RIXIMYO) is a b-lymphocyte antigen cd20 binding agent. Associated with Pfizer Australia Pty Ltd. Route of administration: subcutaneous. Current US regulatory status: approved.

FDA: approved EMA: approved TGA: approved PMDA: approved NMPA: clinical trials Antineoplastic and immunomodulating agents (L01) L01FA01
US status approved
Patents linked 5
Pipeline programs 119
News articles 3
Drug details — rituximab

Quick answer

rituximab (RIXIMYO) is a b-lymphocyte antigen cd20 binding agent. Associated with Pfizer Australia Pty Ltd. Route of administration: subcutaneous. Current US regulatory status: approved.

Key facts

INN rituximab
Brand RIXIMYO
Mechanism B-lymphocyte antigen CD20 binding agent
Target B-lymphocyte antigen CD20
Therapeutic class Antineoplastic and immunomodulating agents (L01)
Route SUBCUTANEOUS
Formulation SOLUTION
ATC code L01FA01

Mechanism of action

B-lymphocyte antigen CD20 binding agent

Primary target: B-lymphocyte antigen CD20

Approval history

Authority Status Date
FDA approved
EMA approved
TGA approved
PMDA approved
NMPA clinical trials

Recent coverage

Pipeline programs

  1. 20190360 Phase 3 · Amgen · Newly diagnosed Philadelphia-negative B-cell precursor Acute
  2. ACE-CL-311 (AMPLIFY) Phase 3 · Anaxis Pharma · Previously untreated Chronic Lymphocytic Leukemia Without de
  3. ACE-LY-308 Phase 3 · Anaxis Pharma · Mantle Cell Lymphoma
  4. APG2575CC301 Phase 3 · Anaxis Pharma · Newly Diagnosed Chronic Lymphocytic Leukemia/Small Lymphocyt
  5. APHP200026 Phase 3 · PARItec · Patients with GPA and inadequate response to standard of car
  6. APHP211057 Phase 3 · PARItec · myelin oligodendrocytes glycoprotein antibody associated dis
  7. APHP240909 Phase 3 · PARItec · Patient with stabilized SSc-ILD (as defined by a decline of
  8. BGB-11417-303CLL-RR1 Phase 3 · BEONE MEDICINES AUS · Relapsed/Refractory Chronic Lymphocytic Leukemia/Small Lymph

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)
  1. US 11896617

    Polynucleotides encoding rituximab-resistant chimeric antigen receptors

    Expires Mon Feb 08 2044 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  2. US 11352426

    CD3 binding polypeptides

    Expires Mon Jun 02 2042 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  3. US 10307481

    CD37 immunotherapeutics and uses thereof

    Expires Mon May 30 2039 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  4. US 10202452

    CD3 binding polypeptides

    Expires Mon Feb 07 2039 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  5. US 10143748

    B-cell reduction using CD37-specific and CD20-specific binding molecules

    Expires Mon Nov 29 2038 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

Frequently asked questions

What is rituximab?

rituximab (RIXIMYO) is a b-lymphocyte antigen cd20 binding agent. Associated with Pfizer Australia Pty Ltd. Route of administration: subcutaneous. Current US regulatory status: approved.

What is the brand name for rituximab?

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

What is the US approval status of rituximab?

rituximab 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.