Drug intelligence / Profile preview

VALO-D102

Development stage
Unknown
Lead developer
Valo Therapeutics
Modality
Viral Vector Vaccines → Recombinant Vaccines → Prophylactic Vaccines → Vaccines & Immunotherapeutics, Cancer Vaccines → Therapeutic Vaccines → Vaccines & Immunotherapeutics, Oncolytic Viruses → Oncolytic Therapeutics
Administration
Intratumoral, Intravenous
01

Overview

VALO-D102 is a genetically modified oncolytic adenovirus developed by Valo Therapeutics. It serves as the viral backbone for the company’s lead immunotherapy product, PeptiCRAd-1. The virus is coated with tumor-specific peptides derived from MAGE-A3 and NY-ESO-1 neoantigens. This design enables selective infection and lysis of cancer cells while simultaneously stimulating both innate and adaptive immune responses against tumors. Mechanistically, VALO-D102 expresses immune-stimulatory molecules CD40L (CD40 ligand) and OX40L (tumor necrosis factor ligand superfamily member 4), which further enhance anti-tumor cytotoxic T-cell immunity by activating antigen-presenting cells and promoting T-cell proliferation. The platform aims to generate robust tumor-specific cytotoxic T-cell responses without requiring multiple genetically engineered viruses for different antigens. VALO-D102/PeptiCRAd-1 is being investigated in combination with pembrolizumab (a checkpoint inhibitor) in Phase I clinical trials for several solid tumors including melanoma, triple negative breast cancer, non-small cell lung cancer, and sarcoma subtypes such as synovial sarcoma and myxoid round cell sarcoma[1][2][3][6][7][9].

Other names
PeptiCRAd-1PeptiCRAd1PeptiCRAd 1Peptide-coated Conditionally Replicating Adenovirus
02

Targets

CD40 (Cluster of differentiation 40 receptor)CD28 (Cluster of Differentiation 28)CD40LG (CD40 ligand extracellular domain)TNFSF4 (Tumor necrosis factor ligand superfamily member 4)

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