Drug intelligence / Profile preview

LVgp120duoCAR

Development stage
Unknown
Lead developer
University of California, San Francisco
Modality
CAR-T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies
Administration
Intravenous
01

Overview

**LVgp120duoCAR** is a lentiviral vector (LV) encoding a bispecific duoCAR architecture for engineering autologous T cells into **LVgp120duoCAR-T cells**, an investigational cell therapy targeting HIV-infected cells. It expresses two distinct chimeric antigen receptors (CARs): one with the mD1.22 domain (engineered CD4 D1 variant) binding the conserved CD4-binding site on HIV-1 gp120, and the other with the m36.4 heavy chain-only antibody domain targeting a CD4-induced (CD4i) epitope near the co-receptor binding site on gp120, linked to 4-1BB costimulatory and CD3ζ signaling domains for enhanced persistence and activation. Developed using HIV-1 lentiviral vectors for efficient T cell transduction, it enables sequential gp120 engagement, potent cytotoxicity (>99% in vitro HIV suppression), cytokine release (IFN-γ, IL-2), and resistance to diverse HIV-1 strains; primary indication is HIV infection management via reservoir reduction, tested in a phase I/IIa dose-escalation trial (NCT04648046) with cyclophosphamide conditioning options and analytic treatment interruption.

02

Targets

HIV-1 gp120 CD4-induced conformationgp120 (HIV-1 envelope glycoprotein (gp120/gp41) epitopes)

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