Drug intelligence / Profile preview

LEISH-F3 + GLA-SE

Development stage
Phase 1
Lead developer
Access to Advanced Health Institute
Modality
Recombinant Proteins and Enzymes, Vaccines & Immunotherapeutics
Administration
Intramuscular
01

Overview

LEISH-F3 + GLA-SE is a vaccine candidate developed for the prevention and treatment of visceral leishmaniasis (VL), a potentially fatal parasitic disease transmitted by sand flies. This vaccine combines recombinant Leishmania proteins with a powerful adjuvant to stimulate immune responses against the parasite. LEISH-F3 + GLA-SE is a recombinant vaccine candidate for the prevention and treatment of visceral leishmaniasis. It consists of the LEISH-F3 fusion protein (containing Leishmania infantum/donovani nonspecific nucleoside hydrolase and Leishmania infantum sterol 24-c-methyltransferase) combined with the GLA-SE adjuvant (glucopyranosyl lipid A formulated as stable emulsion). The vaccine stimulates both humoral and cell-mediated immune responses against Leishmania parasites.

Other names
LEISHMANIA NUCLEOSIDE HYDROLASE-STEROL 24-C-METHYLTRANSFERASE FUSION PROTEIN
02

Targets

Leish-F3 (Leishmania nucleoside hydrolase and sterol 24-c-methyltransferase)TLR4 (Toll-like receptor 4)

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