Drug intelligence / Profile preview

loncastuximab tesirine + durvalumab

Development stage
Unknown
Lead developer
ADC Therapeutics
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

Loncastuximab tesirine + durvalumab is an investigational combination therapy being evaluated for the treatment of relapsed or refractory B-cell lymphomas, including diffuse large B-cell lymphoma (DLBCL), mantle cell lymphoma (MCL), and follicular lymphoma (FL). Loncastuximab tesirine is an antibody-drug conjugate targeting CD19 on B cells; it consists of a humanized monoclonal antibody linked to a pyrrolobenzodiazepine (PBD) dimer cytotoxin. Upon binding to CD19, the conjugate is internalized and releases the PBD toxin, which induces DNA interstrand cross-links leading to cell death. Durvalumab is a monoclonal antibody that inhibits programmed death-ligand 1 (PD-L1), thereby enhancing anti-tumor immune responses. The combination aims to leverage direct cytotoxicity against malignant B cells with immune checkpoint blockade to improve therapeutic outcomes[2][8][1].

Other names
loncastuximab tesirine-lpyl
02

Targets

CD19 (B lymphocyte antigen CD19)DNACD274 (Programmed cell death protein 1 ligand 1)

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