Friday, July 10, 2026

Drug profile · INN

mogamulizumab

mogamulizumab (POTELIGEO) is a c-c chemokine receptor type 4 cross-linking agent. Associated with KYOWA KIRIN AUSTRALIA PTY LTD.

EMA: approved TGA: approved PMDA: approved Antineoplastic and immunomodulating agents (L01) L01XC25
Patents linked 0
Pipeline programs 2
News articles 0
Drug details — mogamulizumab
Class
Antineoplastic and immunomodulating agents (L01)
Route
Patents
0
Programs
2
Data quality
0.83

Quick answer

mogamulizumab (POTELIGEO) is a c-c chemokine receptor type 4 cross-linking agent. Associated with KYOWA KIRIN AUSTRALIA PTY LTD.

Key facts

INN mogamulizumab
Brand POTELIGEO
Mechanism C-C chemokine receptor type 4 cross-linking agent
Target C-C chemokine receptor type 4
Therapeutic class Antineoplastic and immunomodulating agents (L01)
ATC code L01XC25

Mechanism of action

C-C chemokine receptor type 4 cross-linking agent

Primary target: C-C chemokine receptor type 4

Approval history

Authority Status Date
EMA approved
TGA approved
PMDA approved

Pipeline programs

  1. MOGAMULIZUMAB Phase 2 · Ningbo Cancer Hospital · Cutaneous T-cell lymphoma, a category of cancers of lymphocy
  2. POTELIGEO 4 mg/mL concentrate for solution for infusion Phase 2 · Kyowa Kirin International · Mycosis fungoides/Sezary syndrome recurrent

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 mogamulizumab?

mogamulizumab (POTELIGEO) is a c-c chemokine receptor type 4 cross-linking agent. Associated with KYOWA KIRIN AUSTRALIA PTY LTD.

What is the brand name for mogamulizumab?

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