Drug intelligence / Profile preview

IMA401 + pembrolizumab

Development stage
Phase 1
Lead developer
Immatics US, Inc.
Modality
T-cell Engagers → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

IMA401 + pembrolizumab is an investigational combination therapy evaluated for patients with recurrent and/or refractory solid tumors. IMA401 is a bispecific T cell engaging receptor molecule (TCER) designed to target cancer cells expressing the antigens MAGEA4 and MAGEA8, redirecting T cells to kill these tumor cells. Pembrolizumab is a humanized IgG4 monoclonal antibody targeting programmed cell death protein 1 (PD-1), functioning as an immune checkpoint inhibitor to reactivate T cell-mediated antitumor immunity. The combination aims to harness IMA401’s specific T-cell redirection and pembrolizumab’s checkpoint blockade to enhance anti-tumor responses, particularly in tumors with high MAGEA4/8 expression such as head and neck, lung, and bladder cancers. IMA401 is developed by Immatics. Pembrolizumab is developed and manufactured by Merck. The combination is in Phase 1 clinical evaluation for safety, tolerability, initial efficacy, and dose optimization[1][2][3].

Other names
IMA401 TCERIMA-401 TCERIMA 401 TCER
02

Targets

CD3 (T-cell surface glycoprotein CD3)MAGE-A4 peptide-HLA-A*02:01 complexPDCD1 (Programmed cell death protein 1 receptor)MAGEA4 (Melanoma-associated antigen A4)MAGEA8 (Melanoma-associated antigen 8)

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