Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
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].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on IMA401 + pembrolizumab.