Last Updated: 09/02/2026

Malaria: Optimising the mix of malaria interventions including malaria vaccines (OPTiMIX study)

Objectives

Objective 1: Measure the effectiveness, coverage, and safety of national co-implementation of combinations of MVac, PBO-LLINs and chemoprevention (PMC and SMC) at reducing the burden of malaria. This will be achieved through leveraging four large established infant and child cohorts at high risk of malaria. We will extend active and passive cohorts for 3 years to capture the individual and community impacts of various combinations of interventions. The main analysis will use Cox regression on the outcome of clinical malaria.

Objective 2: Identify sustainable and integrated supplementary delivery models to support improved co-implementation of MVac, PBO-LLINs and chemoprevention. This will be achieved by applying a process improvement intervention (the LEAD framework) that supports key stakeholders at different levels of the delivery continuum in co-production and feedback cycles to create sustainable and integrated supplementary delivery models. We will assess supplementary delivery methods and interventions mixes through measures of acceptability and implementation feasibility.

Objective 3: Develop and test a transferable process for assessing and optimising co-implementation of preventive malaria control interventions and elucidating the programme theories underpinning the process. Throughout the study we will build and test programme theories, ultimately deriving final programme theories underpinning MVac, PBO-LLINs and chemoprevention (PMC & SMC) co-implementation.

Principal Investigators / Focal Persons

Roly Gosling

Rationale and Abstract

The aim of this proposal is to evaluate the effectiveness of co-implementation of national strategies of malaria vaccines (MVac), piperonyl butoxide and pyrethroid-treated long-lasting insecticidal nets (PBO-LLINs), and malaria chemoprevention (Perennial Malarial Chemoprevention – PMC and Seaonal Malaria Chemoprevention – SMC) on malaria incidence, and to identify sustainable and integrated supplementary delivery models that optimise acceptability and feasibility to these strategies.
The OPTiMIX study team, a collaboration between the Fobang Institute of Innovation in Science and Technology (FINISTECH) Yaounde, Cameroon, The Institut Nacional de Sante Publique (INSP), Abidjan, Côte d’Ivoire and the London School of Hygiene and Tropical Medicine (LSHTM), London, UK have been working together since 2023 to monitor the roll-out of PMC in moderate-high malaria transmission study sites in Cameroon and Côte d’Ivoire. Each study site consists of a control district where the study population receives standard-of-care malaria prevention, and an intervention district where the population receives the new PMC intervention. The impact of PMC implementation is evaluated using active and passive cohorts to measure incidence of malaria and anaemia, intervention acceptability, feasibility and cost-effectiveness.
In 2024, PMC intervention sites started (or will start) to receive MVacs (RTS,S in Cameroon in March, and R21 in Côte d’Ivoire  in October). In 2025 all study districts will receive PBO-LLINs, and in 2025 our control study district in Côte d’Ivoire will receive SMC. The routine co-implementation of this mix of interventions provides an exciting opportunity to optimise and measure the impacts of combinations of malaria interventions including MVacs.

Date

Jun 2025 — Jan 2029

Total Project Funding

$6.79M

Funding Details
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