Seasonal R21 Mass Vaccination for Malaria Elimination

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

This is a cluster randomized trial to determine the impact of seasonal R21/MM mass vaccination (all ages) on malaria transmission and morbidity. Fifty-four villages (30 in The Gambia and 24 in Burkina Faso) will be randomized to either mass vaccination with R21 or no mass vaccination. The primary objective is to compare in intervention and control clusters the prevalence of malaria (all age groups) at peak transmission after seasonal mass vaccination with R21 (3 monthly doses). Secondary objectives are: 1. To assess the safety and tolerability of R21 through spontaneously reported adverse events. 2. To compare in intervention and control clusters the incidence of malaria infection (all age groups) during the malaria transmission season following seasonal mass vaccination with R21 (3 monthly doses). 3. To compare in intervention and control clusters the incidence of clinical malaria (all age groups) after seasonal mass vaccination with R21 (3 monthly doses). 4. To compare in intervention and control clusters the prevalence of malaria (all age groups) at peak transmission after one booster dose of R21. 5. To compare in intervention and control clusters the incidence of malaria infection (all age groups) during the malaria transmission season following one booster dose of R21. 6. To compare in intervention and control clusters the incidence of clinical malaria (all age groups), after one booster dose of R21. 7. To determine the coverage of seasonal mass vaccination with R21 (primary series of three vaccinations and booster) in intervention clusters and related socio-cultural factors 8. To estimate the cost of seasonal mass vaccination with R21 administration. 9. To estimate the cost-effectiveness of seasonal mass vaccination with R21 compared to standard malaria control measures. The exploratory objective is to determine whether serological markers can detect changes in malaria transmission following mass vaccination with R21.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 5 months
Maximum Age: 99
Healthy Volunteers: t
View:

• Age≥ 5 months.

• Willingness to comply with trial procedures.

• Individual written informed consent obtained at the beginning of the study.

Locations
Other Locations
Burkina Faso
Clinical Research Unit of Nanoro, Burkina Faso
RECRUITING
Nanoro
Gambia
MRC Unit The Gambia at LSHTM
RECRUITING
Fajara
Contact Information
Primary
Umberto D'Alessandro, MD, DHTM, MSc, PhD
Umberto.Dalessandro@lshtm.ac.uk
+220449544
Backup
Anette Erhart, MD, MSs, PhD
Annette.Erhart@lshtm.ac.uk
Time Frame
Start Date: 2024-05-30
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 16200
Treatments
Experimental: Experimental Group
Three monthly doses of R21/MM will be administered to all eligible residents in the 27 intervention villages (15 in The Gambia and 12 in Burkina Faso), starting from May 2024, with the aim of having completed the vaccination schedule by end of July 2024, before the malaria transmission season starts. A booster vaccine dose will be administered in June 2025 to all eligible individuals who received at least one vaccine dose the previous year. Residents who are eligible but not vaccinated in the previous year, will be offered a complete vaccination schedule, i.e. 3 monthly doses, starting from April. After each vaccination, the first 100 vaccinated individuals will be visited at home daily, for 3 consecutive days, and then at day 7 after the vaccination to collect local and systemic adverse events (AE). Vaccinated individuals (or their parents) will be asked to report to the nurse based in their study village any illness occurring during the 28 days after vaccination.
No_intervention: Control Group
Only standard malaria control measures ( Malaria Chemoprevention (SMC), Intermittent Preventive Treatment during pregnancy (IPTp), Insecticide-Treated bed Nets (ITN), prompt diagnosis and treatment of patients with uncomplicated malaria and Indoor Residual Spraying (IRS)) will be implemented in control villages.
Related Therapeutic Areas
Sponsors
Leads: London School of Hygiene and Tropical Medicine
Collaborators: National Malaria Control Programme, The Gambia

This content was sourced from clinicaltrials.gov