Challenge Trial of PfSPZ-LARC2 Vaccine in Burkina Faso

Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-50
SponsorSanaria Inc.

About this trial

This is a randomized, double-blind, placebo-controlled, Phase 1 trial of Plasmodium falciparum (Pf) late liver stage-arresting replication-competent (LARC) sporozoite (SPZ) malaria vaccine (Sanaria® PfSPZ-LARC2 Vaccine) administered to healthy, malaria-exposed adults by direct venous inoculation (DVI) to determine safety, immunogenicity, and efficacy against controlled human malaria infection (CHMI).

The PfSPZ comprising PfSPZ-LARC2 Vaccine contain a double deletion of the genes encoding the Mei2 and LINUP proteins, both of which are required for transition from liver to blood stage malaria. As a result, mei2-/linup- parasites undergo developmental arrest in the late liver stages without releasing merozoites into the blood stream. No blood stage parasites are produced, either asexual or sexual, and the parasite life cycle does not progress.

CHMI will be performed using PfSPZ Challenge (NF54), composed of PfSPZ that are genetically intact and fully infectious. Because PfSPZ-LARC2 vaccine is also based on the Pf strain NF54, CHMI using PfSPZ Challenge (NF54) is considered homologous to the vaccine. It will be performed 6 weeks after the single administration of PfSPZ-LARC2 Vaccine or normal saline placebo (with an option to shorten the interval to 4 weeks if logistical issues arise, such as a risk that CHMI follow-up will overlap with the rainy season).

Eligibility criteria

Qualifiers

Healthy males and females, based on clinical and laboratory findings (note: an effort will be made to recruit roughly equal numbers of males and females, although a balanced sex ratio is not required)

From 18 to 50 years of age

Adults with a Body Mass Index (BMI) 18 to 30 Kg/m²

Residence in the study area for the duration of the study

Disqualifiers

Unable to provide informed consent including inability to pass the test of understanding

Receipt of a malaria vaccine in a prior clinical trial

History of a splenectomy or sickle cell disease.

History of a neurologic disorder (including non-febrile seizures or complex febrile seizures) or formal history of migraine headache

Trial design

Treatments tested in this trial

  • PfSPZ-LARC2 Vaccine
  • PfSPZ Challenge
  • Normal Saline

Treatment groups

45 Participants
are divided into 3 treatment groups

Sponsors and collaborators

Sanaria Inc.

Lead sponsor

University of Maryland, Baltimore

Collaborator

Seattle Children's Hospital

Collaborator

University of California, Los Angeles

Collaborator

Groupe de Recherche Action en Sante

Collaborator