2
项与 LEISH-F2 + MPL-SE Vaccine(Access To Advanced Health Institute) 相关的临床试验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 项与 LEISH-F2 + MPL-SE Vaccine(Access To Advanced Health Institute) 相关的临床结果
100 项与 LEISH-F2 + MPL-SE Vaccine(Access To Advanced Health Institute) 相关的转化医学
100 项与 LEISH-F2 + MPL-SE Vaccine(Access To Advanced Health Institute) 相关的专利(医药)
100 项与 LEISH-F2 + MPL-SE Vaccine(Access To Advanced Health Institute) 相关的药物交易