Drug intelligence / Profile preview

Brenetafusp + chemotherapy

Development stage
Unknown
Lead developer
Immunocore
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Nucleic Acid-Directed Small Molecules → Small Molecules, Recombinant Proteins and Enzymes, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Intravenous
01

Overview

Brenetafusp is a novel ImmTAC (Immune mobilizing monoclonal TCRs Against Cancer) bispecific protein that targets PRAME (PReferentially expressed Antigen in Melanoma), an antigen presented by HLA-A*02:01 on tumor cells. It works by forming a bridge between T-cells and cancer cells, triggering T-cell activation and the release of cytotoxic molecules such as perforin and granzymes, which induce apoptosis in the targeted cancer cells[1][8]. In clinical studies, brenetafusp has demonstrated activity both as monotherapy and in combination with chemotherapy for heavily pre-treated, platinum-resistant ovarian cancer patients[2][5]. The combination with chemotherapy may enhance clinical activity by increasing antigen presentation machinery expression in tumor cells. Brenetafusp is also being investigated for other solid tumors including cutaneous melanoma, non-small cell lung cancer, small cell lung cancer, synovial sarcoma, and endometrial cancers[3][4][8].

02

Targets

DNATUBB (Tubulin (alpha and beta subunits))CD3 (T-cell surface glycoprotein CD3)HLA-A*02 (Human leukocyte antigen A*02 complexed peptide)

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