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Clinical Trials associated with SpFN_1B-06-PL adjuvanted with QS21(WRAIR)A PHASE 1, Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Immunogenicity of Ranging Doses of SARS-COV-2-Spike-Ferritin-Nanoparticle (SPFN_1B-06-PL) Vaccine With Army Liposomal Formulation QS21 (ALFQ) for Prevention of COVID-19 in Healthy Adults.
The purpose of this study is to evaluate the safety, reactogenicity, and immune response of the SpFN COVID-19 vaccine with Army Liposomal Formulation QS21 (ALFQ) adjuvant in healthy adults ages 18-55.
100 Clinical Results associated with SpFN_1B-06-PL adjuvanted with QS21(WRAIR)
100 Translational Medicine associated with SpFN_1B-06-PL adjuvanted with QS21(WRAIR)
100 Patents (Medical) associated with SpFN_1B-06-PL adjuvanted with QS21(WRAIR)
100 Deals associated with SpFN_1B-06-PL adjuvanted with QS21(WRAIR)