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Clinical Trials associated with LEISH-F2 + MPL-SE Vaccine(Access To Advanced Health Institute)A Phase 2, Randomized, Open-Label, Controlled Study to Evaluate the Efficacy, Safety, and Immunogenicity of the LEISH-F2 + MPL-SE Vaccine in the Treatment of Patients With Cutaneous Leishmaniasis
The purpose of this study is to determine the efficacy, safety, and immunogenicity of an investigational vaccine being developed for the treatment of leishmaniasis, including cutaneous leishmaniasis (CL). The vaccine, identified as LEISH-F2 + MPL-SE, consists of a Leishmania protein (LEISH-F2) together with an adjuvant MPL-SE.
Phase 1, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety, Tolerability, and Immunogenicity of the LEISH-F2 + MPL-SE Vaccine in Combination With SSG in the Treatment of Patients With PKDL
A phase 1, randomized, double-blind, placebo-controlled study to evaluate the safety, tolerability, and immunogenicity of three injections of 10 µg LEISH-F2 + 25 µg MPL-SE given at 14-day intervals as an adjunct to standard chemotherapy with sodium stibogluconate (20 mg/kg/day for 40 days) in patients with PKDL.
100 Clinical Results associated with LEISH-F2 + MPL-SE Vaccine(Access To Advanced Health Institute)
100 Translational Medicine associated with LEISH-F2 + MPL-SE Vaccine(Access To Advanced Health Institute)
100 Patents (Medical) associated with LEISH-F2 + MPL-SE Vaccine(Access To Advanced Health Institute)
100 Deals associated with LEISH-F2 + MPL-SE Vaccine(Access To Advanced Health Institute)