drugset / Trial / NCT06862453

Safety, Tolerability and Efficacy of PfSPZ-LARC2 Vaccine Against CHMI in Malaria-Naïve Adults

NCT06862453 ↗

RandomizedSequentialQuadruple-blindPrevention

Summary

This is a randomized, double-blind, placebo-controlled Phase 1 trial of Plasmodium falciparum (Pf) sporozoite (SPZ) late-arresting replication-competent (LARC) malaria vaccine (PfSPZ-LARC2 Vaccine) administered to healthy, malaria-naive study participants in Germany by direct venous inoculation (DVI) to determine safety, tolerability, and vaccine efficacy (VE) against controlled human malaria infection (CHMI). PfSPZ-LARC2 Vaccine contains a deletion of two genes, the Mei2 and LINUP genes, and undergoes developmental arrest in the late liver stages without releasing merozoites into the blood stream (blood stage parasites). The primary objective of the study is to assess the safety and tolerability of administration of PfSPZ-LARC2 Vaccine, with special attention to the adequacy of attenuation, in the intention-to-treat (ITT) population.

Timeline

Start
2026-03-12
Primary completion
2026-09-30
Completion
2026-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject PfSPZ-LARC2 Vaccine Vaccine 200000 unknown Intravenous
Subject PfSPZ-LARC2 Vaccine Vaccine 400000 unknown Intravenous