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Malaria InfectionPhase 4COSAV-R21NCT07038837

Comparison of Two Strategies for Administering the R21-Matrix M Vaccine in a Context of Seasonal Malaria Transmission in Chad

A Phase 4 study testing "Synchronised" arm (intervention) in people with Malaria Infection and Malaria Vaccines, run by Epicentre at 1 site in Chad.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This is a two-arm, cluster-randomised, phase IV trial conducted in Chad to assess the protective efficacy and impact in real-life conditions of a new strategy for administering the R21/MM malaria vaccine, synchronized within a seasonal malaria chemoprevention (SMC) campaign, among children living in areas of high… Read more about this study

Who is it for?
Ages 6 to 59 monthsHealthy volunteers can take part
Conditions the study is for
Malaria Infection, Malaria Vaccines
What is being tested?
"Synchronised" arm (intervention)
Type of treatment
Vaccines
Could I receive a placebo?
No, everyone receives an active treatment
How many people
70,000 participants
Where
1 siteChad
Study dates
16 Jun 2025to Jun 2028
Phase
Phase 4
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 59 months
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • • Routine arm
  • Aged 6 to 11 months at the time of the first R21/MM vaccination (dose 1).
  • Residing in a village participating in the study and randomized to the routine arm.
  • Oral consent provided by the child's parent/guardian.
  • Synchronised arm
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  • Aged 6 to 59 months at the time of the first R21/MM vaccination (dose 1) during the first 3 rounds of SMC (2025).
  • Residing in a village participating in the study and randomized to the synchronized arm.
  • Oral consent provided by the child's parent/guardian.

Who cannot join

  • Exclusion criteria for both arms according to Chad national EPI guidelines
  • Malaria vaccine is not recommended for children with known severe hypersensitivity:
  • To a previous dose of a malaria vaccine
  • To a previous dose of hepatitis B vaccine
  • One of the components of the R21/MM vaccine
  • Mild illness - including respiratory tract infections, mild diarrhoea and fever below 38.5° C - is not a contraindication to R21/MM vaccination. Malnutrition and being HIV-seropositive are also not contraindications to R21/MM vaccination.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Chad1 site, 1 recruiting
  • Medecin sans Frontières

    Moïssala, Mandoul Region

    Ouattara San Maurice, +235 85 15 76 18, San-Maurice.OUATTARA@epicentre.msf.org

    Jessica Sayyad Hilario

    Recruiting

About this study

Official title: Cluster Randomised Non-inferiority Trial Comparing Malaria Incidence When Implementing R21/Matrix-M Synchronized With Seasonal Malaria Chemoprevention Distribution Versus R21/Matrix-M Given Routinely Through the EPI in Two Health Districts in Chad (CoSAV-R21)

This is a two-arm, cluster-randomised, phase IV trial conducted in Chad to assess the protective efficacy and impact in real-life conditions of a new strategy for administering the R21/MM malaria vaccine, synchronized within a seasonal malaria chemoprevention (SMC) campaign, among children living in areas of high seasonal malaria transmission.

In this study, a cluster is defined as the catchment area of a primary care health centre. In Chad, each catchment area is known as a 'zone of responsibility' (French: Zone de Responsibilité' [ZR]).

Read more

Twenty-six (26) of the total 27 ZRs in the districts of Moïssala and Dembo will be randomized in a 1:1 ratio to receive a 4-dose (3 primary doses + 1 booster) R21/MM schedule either (1) integrated into the routine EPI vaccination program (the "Routine" control arm), or (2) synchronized with an annual seasonal malaria chemoprevention (SMC) campaign (the "Synchronized" intervention arm).

Malaria incidence: R21/MM effectiveness will be assessed using the incidence of biologically confirmed clinical malaria (trial primary endpoint). The incidence of clinical malaria will be determined through enhanced surveillance of malaria cases in health centres and hospitals over a 17-month period (August 2025 - December 2026).

Coverage surveys: Cross-sectional surveys (cluster sampling) will be carried out to measure R21/MM vaccine coverage, SMC coverage, coverage of other malaria prevention measures, and coverage of other EPI vaccines.

Nested case-control study: A sub-sample of children admitted to Moïssala District Hospital with severe clinical malaria will be offered the opportunity to participate in a nested case-control study designed to estimate the individual protective efficacy of R21/MM against severe malaria.

Aditionnaly, the INTEGREVAC ancillary study's objective is to evaluate the cost-effectiveness, acceptability and feasibility of the synchronised vaccination strategy in the context of the ongoing COSAV-R21 trial, to inform policy decisions for the effective deployment of malaria vaccines in SMC implementation areas.

Methodology and planned work:

(i) A qualitative study using in-depth interviews (IDIs) and group discussions with key stakeholders at the national, health facility, and community levels, including caregivers of children eligible for vaccination, in Chad, at several points during the trial. We will explore stakeholders' and beneficiaries' perceptions and experiences of the synchronised SMC vaccination strategy (trial intervention arm) compared to age-based vaccine administration under the routine immunisation programme (trial control arm), as well as considerations for implementing these strategies. Interviews with healthcare providers, including those administering R21 and SMC, and community members will assess the feasibility of implementing the integrated vaccination strategy via SMC.

(ii) An economic evaluation including a cost-effectiveness analysis and a nested equity analysis will be conducted. The economic evaluation will include a cost analysis to carefully identify and measure the additional costs associated with adding malaria vaccination to the EPI delivery platform and, separately, to the SMC delivery channel. Analysis of key cost drivers will enable us to identify potential efficiency savings, provide evidence for country funding requests (e.g., to GAVI and the Global Fund) and for the malaria vaccine strategy budgeting/planning process. Cost-effectiveness and equity analyses of each vaccine delivery strategy will provide evidence to help national programmes plan future malaria vaccine delivery and inform global guidance and on methods of delivering these vaccines, while providing valuable evidence on the real-world cost-effectiveness of malaria vaccination.

(iii) Impact modelling will estimate the costs, impact, and cost-effectiveness of scaling up the intervention approach to the whole of Chad, under different temporal and spatial scenarios.

Being tested
"Synchronised" arm (intervention)
Keywords
Vaccine, Malaria, Implementation strategy, Children, Pediatric, synchronized, coverage, prevention, incidence, prevalence, qualitative, mixed methods, cost effectiveness, Seasonal Malaria Chemoprevention
Medical subject headings
Malaria

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • "Synchronised" arm (intervention)Other

    Vaccines received together with CPS

Study groups in NCT07038837
Study groupRoleWhat they receive
"Routine" arm (control)No interventionprimary series (3 doses) of R21/Matrix M administered throughout the year as part of the routine Expanded Programme on Immunisation (EPI), followed by a single booster six months after the 3rd dose.
"Synchronised" arm (intervention)Experimentalprimary series (3 doses) of R21/MatrixM synchronized with a seasonal malaria chemoprevention (SMC) campaign, followed by a single booster 12 months after 1st dose was introduced.
Receives: Other: "Synchronised" arm (intervention)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Malaria incidence in children who were aged 6-11 months when receiving their first dose R21/MM

    To assess whether the R21/MM vaccine synchronized with SMC is non-inferior in preventing malaria (based on malaria incidence) compared to R21/MM administered as part of routine EPI in children who were aged 6-11 months when receiving their first dose R21

    Measured: From enrollment to Month 17 (Aug 2025- december 2026)

Secondary outcomes (8)
  1. Malaria incidence

    Incidence of clinical malaria (biologically confirmed by RDT) in each study arm among children aged 6-59 months, irrespective of R21/MM vaccination status

    Measured: from enrolment to Month 17 (Aug 2025- Dec 2026)

  2. R21/MM vaccination coverage

    Proportion of children having received the appropriate number of doses for their age

    Measured: from enrolment to Month 17 (Aug 2025- Dec 2026)

  3. Coverage of other malaria prevention measures

    SMC coverage: average number of doses received per child and proportion of children receiving 0 and 5 doses

    Measured: From enrolment to month 17 (Aug 2025- Dec 2026)

  4. Coverage of other malaria prevention measures

    Proportion of children possessing, and proportion of children using, a long-lasting insecticidal net (LLIN) on the day before completing the coverage survey questionnaire

    Measured: from enrolment to Month 17 (Aug 2025- Dec 2026)

  5. Coverage of other EPI antigens

    • Proportion of age-eligible children vaccinated against measles-1 and measles-2.

    Measured: from enrolment to Month 17 (Aug 2025- Dec 2026)

  6. Protective efficacy against severe malaria

    Protective efficacy of vaccination with R21/MM will be measured at the individual level against severe malaria confirmed by RDT and microscopy. The protective efficacy will be calculated from the relative risk (RR) of developing severe malaria in vaccinated and unvaccinated children.

    Measured: From enrollment to Month 17 (Aug 2025- december 2026)

  7. Proportional morbidity

    • Proportion of all-cause morbidity registered at health centres attributed to uncomplicated malaria

    Measured: From enrollment to Month 17 (Aug 2025- december 2026)

  8. R21/MM safety

    Frequency of reported serious adverse events (SAEs), adverse events following immunization (AEFI), Serious AEFIs and reported adverse events of special interest (AESIs) following R21/MM vaccination

    Measured: From enrollment to Month 17 (Aug 2025- december 2026)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Jun 2025
  2. Study start16 Jun 2025
  3. Primary completionDec 2026 (estimated)
  4. Study completionJun 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Model description
Synchronization of R21 vaccination with SMC distribution
Masking
None (open label)
Enrolment
70,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07038837
Sponsor's protocol ID
COSAV-R21
Acronym
COSAV-R21
Status last verified
Apr 2026
First submitted
3 Jun 2025
Last updated
15 Apr 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing "Synchronised" arm (intervention) in people with Malaria Infection and Malaria Vaccines, run by Epicentre at 1 site in Chad.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 9 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 15 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Chad. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Jessica SAYYAD, Dr (+331 40 21 55 55, jessica.sayyad@epicentre.msf.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Malaria incidence in children who were aged 6-11 months when receiving their first dose R21/MM (time frame: From enrollment to Month 17 (Aug 2025- december 2026)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Apr 2026.

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