As of September 2, the outbreak had recorded 6,342 cases and 3,072 deaths, making it the second largest Ebola outbreak ever reported in the country and the fastest growing to date.
The guidance recommends that Ervebo® should currently be used against Bundibugyo virus (BDBV) only within a research protocol.
The mobile laboratory forms part of efforts to strengthen Uganda’s public health emergency preparedness following lessons from recent Ebola outbreaks.
Uganda completed the monitoring period without detecting further transmission, providing an additional safeguard that no transmission chains linked to the imported case had been missed.
The ICG will allocate 20,000 doses to a Phase 3 clinical trial designed to assess whether Ervebo can protect people against Bundibugyo virus.
Following a review of the latest epidemiological data, the ECG noted that the DRC had recorded 4,449 confirmed Ebola cases and 2,061 confirmed deaths, representing a case-fatality rate of 46.3%.
The Phase 1 study forms part of an expanded collaboration between Moderna and the Coalition for Epidemic Preparedness Innovations (CEPI).
The initiative comes as scientists intensify efforts to address a major Bundibugyo ebolavirus outbreak, with cases rising rapidly in the Democratic Republic of the Congo (DRC).
Throughout the 42-day period, health authorities maintained enhanced nationwide surveillance and found no evidence of further transmission.
The experimental vaccine was developed by scientists at the University of Oxford using the same vaccine technology employed in the Oxford-AstraZeneca COVID-19 vaccine.