Of Uganda's 20 confirmed cases, 15 were imported from the DRC and five were locally acquired through secondary transmission . Two Congolese nationals died, and one additional probable case also died . The last patient was discharged from a treatment center on July 16, 2026, triggering the 42-day countdown . No new cases were reported in Uganda after June 21, 2026 .
The DRC's Bundibugyo virus outbreak, first reported on May 14, 2026, in Ituri Province, has become one of the largest and fastest-growing Ebola outbreaks on record . The WHO Director-General warned on July 16, 2026, that the outbreak is "outpacing response" efforts despite major mobilization . By comparison, the 2018–2019 Ebola outbreak in the DRC took more than 10 months to reach 2,000 confirmed cases; this outbreak did so in roughly two months .
Key case numbers from official sources:
Beyond the DRC and Uganda, imported cases appeared in Europe: one case in France involved a physician returning from the DRC who fully recovered without secondary transmission, and a case was reported in Germany .
Uganda closed its border with the DRC on May 27, 2026, a temporary measure that permitted crossings only for outbreak response, humanitarian operations, essential cargo, and authorized travelers . All authorized entrants were subjected to strict health screening and monitoring .
The U.S. Centers for Disease Control and Prevention (CDC) issued a Level 4 "Do Not Travel" advisory for Uganda and the DRC on May 27, 2026, and restricted non-essential travel . The U.S. State Department matched the CDC with a Level 4 advisory . Canada also imposed travel restrictions on Uganda and the DRC due to the outbreak.
A critical factor in the outbreak's severity is the absence of any licensed vaccine or treatment specifically for the Bundibugyo virus species . Merck's Ervebo vaccine is licensed only for Zaire ebolavirus, not Bundibugyo . A specific Bundibugyo vaccine candidate (rVΔ/BDB-GP), using the same platform as Ervebo, showed survival benefits in non-human primates but has not been licensed . Animal model data suggest Ervebo may provide partial cross-protection against Bundibugyo, but no clinical evidence existed as of early July . The WHO has recommended that Ervebo should not be used outside carefully designed research settings .
In response, the Africa CDC and partners began organizing clinical trials in the DRC to test whether Merck's Ervebo vaccine can provide cross-protection against the Bundibugyo strain . A July 2026 human serology study published in the New England Journal of Medicine found that Ervebo may offer partial protection, supporting the rationale for the trial . The trials aim to protect frontline health workers in the DRC . However, the African Medicines Agency (AMA) has stated that existing countermeasures are "unlikely to provide adequate protection without adaptation," highlighting the uncertainty .
The response faces severe systemic obstacles:
The end result is a regional picture with two starkly different narratives. Uganda successfully contained its cross-border spillover through rapid border controls, surveillance, and treatment of all confirmed cases. Meanwhile, the DRC epidemic continues to accelerate with no licensed medical countermeasures and severe operational challenges.