Drug intelligence / Profile preview

ALLO-329

Development stage
Phase 1
Lead developer
Allogene Therapeutics
Modality
CRISPR-Cas9 → CRISPR Systems → Programmable Nucleases → Gene Editing → Gene Therapies, CAR-T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies
Administration
Intravenous
01

Overview

ALLO-329 is an investigational allogeneic chimeric antigen receptor T-cell (CAR-T) therapy developed for the treatment of autoimmune diseases. It is a dual-targeting CAR-T product that utilizes CRISPR-based site-specific integration to express two chimeric antigen receptors targeting both CD19+ B cells and CD70+ activated T cells. This approach aims to address immune dysregulation by eliminating pathogenic B cells and activated T cells involved in the pathogenesis of autoimmune diseases. The therapy incorporates Allogene’s proprietary Dagger technology, which is designed to reduce or eliminate the need for lymphodepletion prior to cell infusion, potentially simplifying treatment protocols and expanding patient access. ALLO-329 has received FDA fast track designation for several rheumatologic indications and is being evaluated in a phase 1 basket study (RESOLUTION trial) across multiple autoimmune conditions including systemic lupus erythematosus (SLE), idiopathic inflammatory myopathies (IIM), scleroderma/systemic sclerosis (SSc), and lupus nephritis[1][3][4][5][6].

Other names
dual CD19-CD70 CAR-TCD19/CD70 dual AlloCAR T
02

Targets

CD70 (Cluster of Differentiation 70)CD19 (B lymphocyte antigen CD19)

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