Funding request for EBO-PEP response to Bundibugyo outbreak in DRC

Grant number: 356800/Z/26/Z

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Key facts

  • Disease

    Ebola
  • Start & end year

    2026
    2028
  • Known Financial Commitments (USD)

    $8,674,388.68
  • Funder

    Wellcome Trust
  • Principal Investigator

    Lara Pandya
  • Research Location

    Belgium
  • Lead Research Institution

    Global Health EDCTP3
  • Research Priority Alignment

    N/A
  • Research Category

    Therapeutics research, development and implementation
  • Research Subcategory

    Phase 3 clinical trial
  • Special Interest Tags

    N/A
  • Study Type

    Clinical
  • Clinical Trial Details

    Clinical Trial, Phase III
  • Broad Policy Alignment

    Pending
  • Age Group

    Children (1 year to 12 years)
  • Vulnerable Population

    Pregnant women, Other
  • Occupations of Interest

    Unspecified

Abstract

EDCTP funded the EBO-PEP project in 2024 to evaluate a post-exposure prophylaxis (PEP) strategy against Ebola virus disease, establishing a robust outbreak research platform rapidly activatable across filovirus species. To respond to the current Bundibugyo (BVD) outbreak in Eastern Democratic Republic of Congo (DRC), the consortium seeks to mobilise the infrastructure, partnerships, and operational capacities already in place. Obeldesivir (ODV), an orally administered broad-spectrum antiviral prioritized by the WHO R&D Blueprint, is evaluated as PEP in a randomized trial. Remdesivir (RDV) is proposed for vulnerable populations excluded from the randomized trial. EBO- PEP brings together African and European institutions with complementary expertise in filovirus research and clinical trial implementation in outbreak settings. The overall objective of this project is to increase the portfolio of therapeutic tools against BVD by evaluating a PEP strategy for high-risk contacts in Eastern DRC. The two specific objectives are: (i) to set up a randomised, placebo-controlled phase III trial in Eastern DRC to test the efficacy of ODV used as PEP for high-risk contacts; ii) to set up a parallel prospective interventional cohort to generate evidence on the safety, feasibility, and effectiveness of RDV as PEP in children under 12 years and pregnant or breastfeeding women.