Drug intelligence / Profile preview

atezolizumab + bevacizumab + cyclophosphamide

Development stage
Unknown
Lead developer
Genentech
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral (cyclophosphamide, Optional), Intravenous (standard For All Three In Oncology Settings)
01

Overview

**Atezolizumab + bevacizumab + cyclophosphamide** is an investigational combination regimen used primarily in the context of clinical trials for cancer therapy. - **Atezolizumab** is a monoclonal antibody targeting the immune checkpoint protein PD-L1, inhibiting the interaction with PD-1 and B7.1 to activate antitumor immune responses (checkpoint inhibitor, immunotherapy)[1][3]. - **Bevacizumab** is a monoclonal antibody that binds to vascular endothelial growth factor A (VEGF-A), inhibiting angiogenesis and tumor blood vessel formation (targeted therapy)[1][3]. - **Cyclophosphamide** is a small molecule alkylating agent that crosslinks DNA, causing cell death and immunosuppression; it is used in numerous regimens against various cancers[2][4]. This three-drug combination has potential applications in solid tumors, especially those where atezolizumab + bevacizumab is already established (e.g., hepatocellular carcinoma), and cyclophosphamide is added to enhance antitumor efficacy or modulate the immune microenvironment.

02

Targets

DNAVEGFA (Vascular endothelial growth factor A)CD274 (Programmed cell death protein 1 ligand 1)

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