Drug intelligence / Profile preview

durvalumab + tremelimumab + vinorelbine

Development stage
Unknown
Lead developer
AstraZeneca
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Intravenous
01

Overview

This is a combination therapy consisting of three drugs: durvalumab, tremelimumab, and vinorelbine. Durvalumab is a human monoclonal antibody targeting programmed death-ligand 1 (PD-L1), acting as an immune checkpoint inhibitor to enhance anti-tumor immune responses. Tremelimumab is a fully human IgG2 monoclonal antibody that targets cytotoxic T lymphocyte-associated antigen 4 (CTLA-4), another immune checkpoint, further promoting T cell-mediated tumor destruction. Vinorelbine is a semi-synthetic vinca alkaloid chemotherapy agent that inhibits microtubule assembly, disrupting mitosis in cancer cells. This combination has been investigated in phase I/II clinical trials for advanced solid tumors, including advanced cervical cancer and breast cancer, showing promising antitumor activity and manageable safety profiles[1][2][8]. The regimen leverages both immunotherapy and chemotherapy mechanisms to improve outcomes in patients with refractory or recurrent cancers.

Other names
MEDI4736MEDI-4736MEDI 4736ticilimumab
02

Targets

CTLA-4 (Cytotoxic t-lymphocyte–associated protein 4)CD274 (Programmed cell death protein 1 ligand 1)TUBB (Tubulin (alpha and beta subunits))

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