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Last Updated: 27/10/2022
A study to determine if a new Malaria vaccine is safe and induces immunity among Kenyan adults, young children and infants.
Objectives
To evaluate the safety and immunogenicity of different doses of a candidate Malaria vaccine; adjuvanted R21(R21/MM) in adults, young children and infants in Kilifi, Kenya.
Principal Institution
Principal Investigators / Focal Persons
Rationale and Abstract
This is a clinical trial to evaluate the safety and immunogenicity of R21/MM in healthy Kenyan participants from the different age groups.
The study includes three age groups:
Group 1: healthy adults (18-45 years)
Group 2: young children (aged 1-5 years)
Group 3: infants (aged 5- <12 months of age)
Each group will receive 3 vaccine doses which will be 4-weeks apart.
NCT number: NCT03580824
Study Design
Study type: Interventional
Enrollment: 91 participants
Allocation: Non-Randomized
Intervention model: Parallel Assignment
Masking: None (Open Label)
Primary purpose: Treatment
External reference
Thematic Categories
Date
Apr 2019 — Jun 2022
Funding Details
Project Site
Related Resources
