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TAMAVAQ NeoVaccine + Poly-ICLC + cGAMP + granulocyte-macrophage colony stimulating factor + imiquimod + CpG oligodeoxynucleotides + saponins + monophosphoryl lipid A
- Development stage
- Unknown
- Lead developer
- Biogenea
- Modality
- Small Molecules, MicroRNA (miRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Cytokines & Interferons → Recombinant Proteins and Enzymes, Vaccines & Immunotherapeutics
- Administration
- Intradermal, Subcutaneous, Topical (imiquimod), Possibly Others Depending On Component
01
Overview
This investigational combination immunotherapy comprises TAMAVAQ NeoVaccine, a personalized cancer vaccine, co-administered with several innate immune system adjuvants and stimulators, including Poly-ICLC (a synthetic double-stranded RNA agonist), cGAMP (a STING agonist), granulocyte-macrophage colony stimulating factor (GM-CSF), imiquimod (a TLR7 agonist), CpG oligodeoxynucleotides (TLR9 agonists), saponins (plant-derived adjuvants), and monophosphoryl lipid A (TLR4 agonist). The aim is to elicit a robust anti-tumor immune response. The combination is under investigation primarily for glioblastoma, with a focus on safety and immunogenicity[1][2].
02
Targets
CSF2R (Granulocyte-macrophage colony-stimulating factor receptor)TLR7 (Toll-like receptor 7)TLR3 (Toll-like receptor 3)STING (Stimulator of interferon genes protein)Cell membrane cholesterol-rich microdomainγδ TCR (T-cell receptor)TLR9 (Toll-like receptor 9)TLR4 (Toll-like receptor 4)
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