Drug intelligence / Profile preview

TAR-200 + cetrelimab

Development stage
Unknown
Lead developer
Johnson & Johnson
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravesical (TAR-200 - Device Placed In Bladder), Intravenous (cetrelimab - Infusion)
01

Overview

TAR-200 + cetrelimab is an investigational combination therapy for bladder cancer, currently in clinical development. **TAR-200** is a novel intravesical drug delivery system enabling sustained local release of gemcitabine directly into the bladder via minitablets in an osmotic device. **Cetrelimab** is a fully human monoclonal antibody of the IgG4 subclass targeting the programmed cell death receptor-1 (**PD-1**), acting as an immune checkpoint inhibitor. Combined, TAR-200 provides localized chemotherapy while cetrelimab potentiates immune-mediated anti-tumor activity by blocking the PD-1 axis, enhancing T cell responses and reversing immunosuppressive signaling in the tumor microenvironment. The combination is being evaluated for its safety and efficacy in neoadjuvant and non-muscle invasive bladder cancer settings, especially in patients who are ineligible for or refuse platinum-based chemotherapy or radical cystectomy. Both components are developed and investigated by Janssen (Johnson & Johnson)[1][3][5][7].

Other names
TAR-200 and cetrelimabTAR200 and cetrelimabTAR 200 and cetrelimabTAR-200 + CET
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)

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