Efficacy, Safety and Immunogenicity Evaluation of MTBVAC in Newborns in Sub-Saharan Africa

Recruiting now · Phase 3

Conditions studied: Tuberculosis

In brief

The objective of this project is to demonstrate safety, immunogenicity and improved efficacy of the new live attenuated M. tuberculosis vaccine called MTBVAC in a Phase 3 efficacy trial in HIV-uninfected infants born to HIV-infected and HIV-uninfected mothers as compared to standard of care BCG vaccination. The proposal builds upon a group of TB vaccine development partners in Europe and sub-Saharan Africa established in a previous EDCTP-supported project. It creates an expanded consortium of clinical trial partners for the optimal implementation of a large infant efficacy trial of MTBVAC in high TB incidence settings. New capacity for efficacy trials in infants will be a valuable resource for the TB vaccine development community. The proposal will create a network of institutions in three TB endemic African countries with enhanced laboratory capacity to conduct TB vaccine immunology studies and to bio-bank samples to discover immune correlates of vaccine-mediated protection.

Key facts

Study ID

NCT04975178

Run by

Biofabri, S.L

People needed

7120

Starts

2022-10-17

Expected to finish

2029-02-01

Last updated by the study team

2025-02-10

Who can join

Age: any, up to 0. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Male or female newborns within seven days of birth.
• Written informed maternal consent, including permission to access maternal antenatal, postnatal, and infant medical records.
• Infant participants and their caregivers available for trial follow-up and display the willingness and capacity to comply with trial procedures.
• Newborns must be in good general health during pregnancy and delivery, as assessed by medical history and targeted physical examination.
• Birth weight ≥ 2450 grams.
• Apgar score at 5 minutes ≥ 7.
• A maternal HIV test result (rapid test, enzyme-linked immunosorbent assay (ELISA), or Polymerase chain reaction (PCR)) taken within 30 days of delivery, or within seven days post-partum must be available and documented if HIV uninfected. If the mother is HIV infected, then she must be on antiretroviral (ARV) therapy as per in-country guidelines with a viral load of <50 copies/mL (within six months of labour).
• Estimated gestational age ≥ 37 weeks.
• Mother has not participated in a clinical trial within three months prior to the infant's birth.
• Mother has never participated in a TB vaccine trial before.
• Infant may not participate in any other clinical trials.

You may not qualify if…

• Receipt of BCG vaccination prior to enrolment.
• Significant antenatal, intrapartum, or postpartum complications that may affect the health of the newborn.
• Skin condition, bruising or birth mark at the intended injection site.
• Maternal HIV test (rapid test, ELISA, or PCR) result not available.
• HIV exposed Newborn's HIV PCR result positive or not available.
• Maternal history of TB during pregnancy.
• History of close/household contact with a TB patient, antenatal or postnatal, whether maternal, other family member or another household member who has not yet completed TB treatment.
• Clinically suspected neonatal sepsis.
• Any severe congenital malformation.
• History or evidence of any systemic disease on examination, or any illness that in the opinion of the Investigator may interfere with the evaluation of the safety and immunogenicity of the vaccine. Neonatal jaundice not considered clinically significant is not an exclusion.

Where it is running

• South African Tuberculosis Initiative, Brewelskloof Hospital — Worcester, Western Cape, South Africa (enrolling)

Full record on ClinicalTrials.gov

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