Drug intelligence / Profile preview

bintrafusp alfa + cisplatin

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

Overview

**Bintrafusp alfa + cisplatin** is an investigational combination therapy consisting of bintrafusp alfa—a recombinant bifunctional fusion protein that targets two key immunosuppressive pathways—and cisplatin, a platinum-based chemotherapeutic. Bintrafusp alfa functions by simultaneously blocking transforming growth factor beta (TGF-β) via receptor "trap" and programmed death-ligand 1 (PD-L1) via monoclonal antibody blockade, designed to enhance antitumor immune responses. Cisplatin crosslinks DNA, leading to apoptosis in cancer cells. This combination has been studied in the treatment of advanced biliary tract cancer and locally advanced, persistent, recurrent, or metastatic cervical cancer, primarily in first-line settings. The drug combination is under development by Merck KGaA (bintrafusp alfa) and is used in combination with standard platinum-based chemotherapy regimens[1][3].

02

Targets

DNACD274 (Programmed cell death protein 1 ligand 1)TGFB (GARP–latent transforming growth factor beta 1 complex)

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