Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
IMA402 + chemotherapy + monoclonal antibody is an investigational combination regimen being evaluated for the treatment of PRAME-positive solid tumors. The primary component, IMA402, is a next-generation, half-life extended bispecific T cell engaging receptor (TCER®) molecule developed by Immatics. It is designed to target a peptide derived from the Preferentially Expressed Antigen in Melanoma (PRAME) presented by HLA-A*02:01. By binding both the PRAME-HLA complex on tumor cells and the CD3 receptor on T cells, IMA402 redirects T cell cytotoxicity toward the cancer cells. The combination with chemotherapy and a monoclonal antibody is being investigated in Phase Ib/II clinical trials (NCT05958121) to potentially enhance anti-tumor activity in patients with recurrent or refractory solid tumors, including cutaneous and uveal melanoma, ovarian cancer, lung cancer, uterine cancer, and synovial sarcoma.
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 IMA402 + chemotherapy + monoclonal antibody.