Safety, Immunogenicity and Efficacy of R21 Matrix-M in 5-17 Month Old Children in Nanoro, Burkina Faso

University of Oxford450 enrolled

Overview

This is a double blind randomised controlled clinical trial to evaluate the efficacy of R21 adjuvanted with Matrix-M in healthy 5-17 month old children in a malaria endemic area.

In this double-blind, randomised, controlled, phase 2b trial, the low-dose circumsporozoite protein-based vaccine R21, with two different doses of adjuvant Matrix-M (MM), was given to children aged 5-17 months in Nanoro, Burkina Faso-a highly seasonal malaria transmission setting. Three vaccinations were administered at 4-week intervals before the malaria season, with a fourth dose 1 year later. All vaccines were administered intramuscularly into the thigh. Group 1 received 5 μg R21 plus 25 μg MM, group 2 received 5 μg R21 plus 50 μg MM, and group 3, the control group, received rabies vaccinations. Children were randomly assigned (1:1:1) to groups 1-3. An independent statistician generated a random allocation list, using block randomisation with variable block sizes, which was used to assign participants. Participants, their families, and the local study team were all masked to group allocation. Only the pharmacists preparing the vaccine were unmasked to group allocation. Vaccine safety, immunogenicity, and efficacy were evaluated over 1 year. The primary objective assessed protective efficacy of R21 plus MM (R21/MM) from 14 days after the third vaccination to 6 months. From May 7 to June 13, 2019, 498 children aged 5-17 months were screened, and 48 were excluded. 450 children were enrolled and received at least one vaccination. 150 children were allocated to group 1, 150 children were allocated to group 2, and 150 children were allocated to group 3. The final vaccination of the primary series was administered on Aug 7, 2019. R21/MM had a favourable safety profile and was well tolerated. Please see publication for more details: Lancet. 2021 May 15;397(10287):1809-1818. doi: 10.1016/S0140-6736(21)00943-0 After the first booster vaccination, participants in Groups 1 and 2 were further randomised 2:1 to receive R21 with Matrix-M: control. The trial was extended by a further two years with yearly boosters of R21/MM or rabies vaccine. Groups 1 and 2 were subdivided and randomized 2:1 to receive R21/MM or rabies vaccine as the second booster. Group 3 received control rabies vaccine as they had done previously. The second boosting occurred between June and July 2021 where 368 participants were boosted. In May 2022 it was decided to amend the protocol to allow for groups 1a and 2a (malaria vaccine groups) to be randomised 1:1 to receive either the R21/Matrix-M vaccine or a control rabies vaccine a year after the previous booster vaccine. The third boosting occurred between June and July 2022 where 357 participants were boosted. Between June 2, and July 2, 2020, 409 children returned to receive a booster vaccine. Each child received the same vaccination for the booster as they received in the primary series of vaccinations; 132 participants received 5 μg R21 adjuvanted with 25 μg Matrix-M, 137 received 5 μg R21 adjuvanted with 50 μg Matrix-M, and 140 received the control vaccine. A booster dose of R21/Matrix-M at 1 year following the primary three-dose regimen was administered. The trial is ongoing to assess long-term follow-up of these participants and the value of further booster Please see publication for more details of results of two year follow up: Lancet Infect Dis. 2022 Dec;22(12):1728-1736. doi: 10.1016/S1473-3099(22)00442-X. VAC076 is complete, with the last volunteer last visit occurring in July 2023. This trial was funded by the European and Developing Countries Clinical Trials Partnership (reference: RIA2016V-1649 MMVC).

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

450

Conditions

Malaria,Falciparum

Interventions

R21 adjuvanted with 25mcg Matrix-MBIOLOGICAL

Vaccine

Rabies VaccineBIOLOGICAL

Vaccine

R21 adjuvanted with 50mcg Matrix-MBIOLOGICAL

vaccine

Eligibility

Sex: ALLMin age: 5 MonthsMax age: 17 MonthsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Healthy child aged 5-17 months at the time of first study vaccination * Provide written Informed consent of parent/guardian * Child and parent/guardian resident in the study area villages and anticipated to be available for vaccination and follow-up for 2 years following last dose of vaccination Exclusion Criteria: * Clinically significant skin disorder (psoriasis, contact dermatitis etc.), immunodeficiency, cardiovascular disease, respiratory disease, endocrine disorder, liver disease, renal disease, gastrointestinal disease, neurological illness. * Weight-for-age Z score of less than -3 or other clinical signs of malnutrition. * History of allergic reaction, significant IgE-mediated event, or anaphylaxis to immunisation. * History of allergic disease or reactions likely to be exacerbated by any component of the vaccines, e.g. neomycin. * Sickle cell disease. * Clinically significant laboratory abnormality as judged by the study clinician. * Blood transfusion within one month of enrolment. * Administration of immunoglobulins and/or any blood products within the three months preceding the planned administration of the vaccine candidate. * Previous vaccination with experimental malaria vaccines. * Participation in another research study involving receipt of an investigational product in the 30 days preceding enrolment, or planned use during the study period. * Current participation in another clinical trial, or within 12 weeks of this study. * Known maternal HIV infection (No testing will be done by the study team). * Any confirmed or suspected immunosuppressive or immunodeficient state, including HIV infection; asplenia; recurrent, severe infections and chronic (more than 14 days) immunosuppressant medication within the past 6 months (For corticosteroids, this will mean prednisone, or equivalent, \>= 0.5 mg/kg/day. Inhaled and topical steroids are allowed). * Any significant disease, disorder or situation which, in the opinion of the Investigator, may either put the participants at risk because of participation in the trial, or may influence the result of the trial, or the participant's ability to participate in the trial.

Locations (1)

Institut de Recherche en Sciences de la Sante - Clinical Research Unit of Nanoro (IRSS-URCN)

Nanoro, Burkina Faso

Outcomes

Primary Outcomes

The protective efficacy (number of cases) against clinical malaria of R21 adjuvanted with Matrix-M in 5-17 month old children living in a malaria-endemic area

We will look for the presence of axillary temperature ≥37.5°C AND P. falciparum parasites density \> 5000 asexual forms/µL as a primary case definition of clinical malaria. \- We will look for the presence of axillary temperature ≥37.5°C and/ or history of fever within the last 24 hours AND P. falciparum parasites density \> 0 for a secondary case definition of clinical malaria.

Time frame: for 6 months after the last vaccination

Secondary Outcomes

Duration of Protective efficacy (number of cases) against clinical malaria

To assess the protective efficacy (number of cases) against clinical malaria of R21 adjuvanted with Matrix-M in 5-17 months old children living in a malaria-endemic area

Time frame: for 12 months after administration of the third dose of vaccine, and for 6 and 12 months after each booster vaccination

Efficacy (number of cases) against asymptomatic P. falciparum infection

Primary case definition of asymptomatic P. falciparum infection: Presence of axillary temperature \< 37.5°C and absence of history of fever within the last 24 hours; AND P. falciparum parasites density \> 0 asexual forms/µL

Time frame: at 6 and 12 months after administration of the third dose of vaccine, and for 12 months after each booster vaccination

The safety and reactogenicity (number of adverse events) of R21 adjuvanted with Matrix-M in 5-17 month olds living in a malaria-endemic area in the month following each vaccination and at 12 months after administration of the final dose of vaccine

* Occurrence of solicited local and/or systemic reactogenicity signs and symptoms for 7 days following the vaccination * Occurrence of unsolicited adverse events for 28 days following the vaccination * Occurrence of serious adverse events for the duration of the trial

Time frame: for 6 and 12 months after administration of the third dose of vaccine, and for 12 months after each booster vaccination

Data from ClinicalTrials.gov

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