Drug intelligence / Profile preview

VCL-CT02

Development stage
Phase 1
Lead developer
Vical
Modality
DNA Vaccines → Plasmid DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Prophylactic Vaccines → Vaccines & Immunotherapeutics
Administration
Intradermal, Intramuscular
01

Overview

**VCL-CT02** is an investigational trivalent plasmid DNA vaccine developed by Vical for prevention of human cytomegalovirus infection. The vaccine contains three codon-optimized plasmid DNA constructs in phosphate-buffered saline that encode the human cytomegalovirus antigens pp65, glycoprotein B, and immediate-early protein 1, derived from the AD169 strain. Following administration, host-cell expression of these viral antigens is intended to induce CMV-specific cellular and humoral immune responses. VCL-CT02 was evaluated in Phase 1 studies in healthy CMV-seronegative adults by intramuscular and intradermal administration, including studies in which it primed subjects before challenge with the live-attenuated Towne CMV vaccine. ([clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00373412))

Other names
VCL CT02 pDNA vaccinetrivalent pDNA CMV vaccine
02

Targets

pp65 (Cytomegalovirus phosphoprotein 65)gB (Human cytomegalovirus glycoprotein B)IE1 (HCMV immediate-early protein 1)

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