CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 478 enrolled
Drug / intervention
PfSPZ Vaccine +2 morebiological
Likely dose
artemether 20mg/lumefantrine 120mg (AL)from record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03510481
NCT03510481Phase 1Completed

Randomized, Placebo-Controlled, Double-Blind Study to Assess Safety, Immunogenicity, and Protective Efficacy of Two Regimens of Radiation Attenuated Plasmodium Falciparum NF54 Sporozoites (PfSPZ Vaccine) During Natural Transmission Season in Healthy African Adults in Mali

National Institute of Allergy and Infectious Diseases (NIAID)·interventional·Posted Apr 27, 2018·Updated Aug 20, 2021

In Brief

A Phase 1 clinical trial evaluating PfSPZ Vaccine, Normal Saline, and 1 other intervention for Malaria. Completed, enrolled 478 participants across 1 site.

Detailed Summary

Background: The disease malaria affects many people in Mali and other parts of Africa and the world. It is caused by germs spread by mosquito bites. Malaria may be mild. But it can also be serious or lead to death if it is not treated promptly. Researchers want to find a safe vaccine that prevents malaria. Objective: To study how safe and tolerable the malaria vaccine called PfSPZ Vaccine is for healthy adults. Eligibility: Healthy adults: * ages 18-35 in Ouelessebougou, Mali * not infected with HIV, hepatitis B, or hepatitis C * for females, not pregnant or breastfeeding and must use reliable birth control during the study Design: Participants will be screened with questions about malaria and will undergo blood, urine, and heart tests. Participants will be randomly assigned to 1 of 4 groups. They will get injections of either the PfSPZ Vaccine or a salt-water placebo. They will not know which one they get. Vaccinations will occur leading into the malaria transmission each year with 3 injections leading into Year 1 (malaria transmission season in 2018) and 1 injection prior to Year 2 (malaria transmission season 2019). One vaccine group and one placebo group will get an injection 3 times over 4 weeks with an additional vaccination \~10 months later. The other two groups (vaccine group and placebo) will get an injection 3 times over 16 weeks with an additional vaccination \~10 months later. All participants will be treated with an antimalarial medication prior to the third injection and prior to fourth injection. They will be followed for approximately 6 months after third and fourth injection. At vaccine visits, female participants will have a pregnancy test before injection. All participants will have an arm cleaned and the vaccine injected in a vein. They will be watched for 30 minutes. At non-vaccine visits, participants will have a physical exam and be asked how they are feeling. They will usually have blood tests.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMalaria
CountriesMali

Timeline

Phase 1CompletedFinished
20192020202120222023202420252026
First PostedApr 27, 2018
Enrollment StartMay 14, 2018
Primary CompletionNov 23, 2019
Study CompletionFeb 13, 2020
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 8.2 years ago

Interventions

PfSPZ Vaccinebiological

PfSPZ Vaccine is Radiation attenuated, aseptic, purified, vialed, cryopreserved, NF54 P. falciparum sporozoites produced by Sanaria, Inc.

Normal Salinedrug

Clear liquid indistinguishable from the study product will be used as a placebo rather than a comparator vaccine.

artemether 20mg/lumefantrine 120mg (AL)drug

Licensed antimalarial in the US and Mali for use for uncomplicated malaria.