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. Author manuscript; available in PMC: 2021 Jun 17.
Published in final edited form as: Curr Issues Mol Biol. 2020 Sep 23;41:469–508. doi: 10.21775/cimb.041.469

Table 1.

Summary of clinical trial results with HSV vaccine candidates

Name Platform Antigens Immune
Response
Clinical Results
gB/gD/MF59 (Chiron) Subunit MF59 adjuvant gD and gB Neutralizing Abs Phase 3 Prophylaxis 9% (95% CI: −29%, 36%)
gD/AS04 (GSK) Subunit AS04 adjuvant gD Neutralizing Abs CD4+ T cells Phase 3 Prophylaxis 20% (95% CI: −29%, 50%)
gH-null (Cantab Pharmaceuticals) Single-cycle live Multiple Neutralizing Abs Phase 3 therapeutic No difference in recurrences or shedding
HSV529 (Sanofi-Pasteur) Replication-defective Multiple Neutralizing Abs CD4, CD8 T cells Phase 1 Safe but immunogenic in doubly-seronegatives only
Gen-003 (Genocea) Subunit Saponin adjuvant gD, ICP4 Neutralizing Abs Cytolytic T cells Phase 2 therapeutic Dose variable decrease shedding
HerpV (Agenus) Heat shock protein 70-HSV peptides QS-21 adjuvant 32 HSV peptides (gD, additional envelope, tegument, and other) Cytotoxic T cells Phase 2 therapeutic 17% reduction in shedding frequency
Vaxfectin (Vical) DNA Vaxfectin adjuvant gD, UL46/47 Neutralizing Abs Phase 1/2 therapeutic Failed to reduce shedding
COR-1 (Admedus) Codon optimized DNA Codon optimized gD2 and ubiquitin-fused truncated gD2 to target the antigen to the proteasome gD-specific Abs Cytotoxic T cells Phase 2 therapeutic No difference in recurrences
ΔNLS (Rational Vaccines) Deleted in ICP0 Replication competent Attenuated for latency Multiple targets Neutralizing Abs gD-specific Abs Phase 1 non-FDA approved therapeutic study Self-reported reduction in recurrences