Drug intelligence / Profile preview

SPARK

Development stage
Preclinical
Lead developer
University of Pennsylvania
Modality
Gene Therapies, Plasmid DNA → DNA Therapeutics → Nucleic Acid Therapeutics
Administration
Intratumoral
01

Overview

SPARK (Systemic Plasmid-Activated Response Kit) is an experimental intratumoral gene therapy designed to overcome the immunosuppressive tumor microenvironment and induce a systemic anti-tumor response. It consists of plasmids encoding the pro-inflammatory cytokine Interleukin-12 (IL-12), the T-cell-recruiting chemokine CXCL9, and a membrane-bound single-chain variable fragment (scFv) against CD3 (specifically clone 145-2C11 in preclinical models). Delivered via in vivo electroporation, SPARK aims to locally "inflame" the tumor lesion, recruit effector T cells, and provide a potent TCR-mimetic stimulus. This sequential activation leads to the expansion of tumor-specific T cells that can circulate and target distal, untreated lesions, a phenomenon known as the abscopal effect. Preclinical studies have demonstrated its efficacy in inducing regression of both treated and untreated tumors in various cancer models.

Other names
plasmid IL-12 + CXCL9 + anti-CD3IL-12/CXCL9/anti-CD3 plasmid combinationSystemic Plasmid-Activated Response Kit
02

Targets

CXCL9 (C-X-C motif chemokine ligand 9)CD3 (T-cell surface glycoprotein CD3)IL12 (Interleukin-12)

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