Drug intelligence / Profile preview

bintrafusp alfa + cisplatin + paclitaxel

Development stage
Phase 1
Lead developer
Merck KGaA
Modality
Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes, Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

bintrafusp alfa + cisplatin + paclitaxel is a combination therapy comprising bintrafusp alfa, a bifunctional fusion protein targeting both programmed death ligand 1 (PD-L1) and transforming growth factor beta (TGFβ); cisplatin, a platinum-based chemotherapy; and paclitaxel, a microtubule-stabilizing agent. Bintrafusp alfa functions as both an immune checkpoint inhibitor and a TGFβ "trap," enhancing antitumor immune responses and reversing immune resistance. Cisplatin and paclitaxel are cytotoxic chemotherapies commonly used in various solid tumors. This combination is being investigated mainly in the context of HPV-associated malignancies and other advanced cancers, aiming to exploit both immunotherapy and chemotherapy mechanisms for potentially synergistic effects, especially where TGFβ-mediated immunosuppression and chemoresistance are key issues[1].

02

Targets

DNACD274 (Programmed cell death protein 1 ligand 1)TGFB (GARP–latent transforming growth factor beta 1 complex)TUBB (Tubulin (alpha and beta subunits))

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