ClinConnect ClinConnect Logo
Search / Trial NCT06841614

EBOla Post-Exposure Prophylaxis

Launched by ANRS, EMERGING INFECTIOUS DISEASES · Feb 18, 2025

Trial Information

Current as of July 24, 2025

Not yet recruiting

Keywords

Ebola Virus Disease Ebov High Risk Contact Post Exposure Prophylaxis

ClinConnect Summary

The EBO-PEP trial is a study designed to test new ways to prevent Ebola Virus Disease (EVD) in people who are at high risk of getting the virus after being in contact with someone who has it. This trial will include individuals who have had direct contact with someone showing symptoms of EVD, like diarrhea or vomiting, or with the body fluids of someone infected. To participate, individuals must be at least 6 months old, have had their last contact within the last 5 days, and show no signs of EVD.

Participants will be divided into two groups: one will receive a vaccine called Ervebo, while the other will receive Ervebo along with another treatment called Inmazeb, followed by a second dose of the vaccine later. Throughout the trial, participants will be closely monitored for at least 21 days, with regular visits to a health center and daily check-ins to ensure their health and safety. If any symptoms of EVD develop, participants will be assessed and treated at a specialized Ebola Treatment Center. This study aims to find the best way to protect those who are most vulnerable to this serious disease.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Last high-risk contact within the last 5 days
  • No signs or symptoms of EVD
  • Age ≥ 6 months
  • Signed and dated informed consent (by a representative of parental authority for minors).
  • Exclusion Criteria:
  • Previous vaccination with Ervebo or any other EVD vaccine less than 5 years ago (declared by the participant)
  • History of confirmed EVD less than 5 years ago (declared by the participant);
  • Hypersensitivity to one of the investigational medicinal products (IMP) or to their excipients (declared by the participant)
  • Participation in another therapeutic or vaccination trial for EVD
  • Any other reason which, at the investigator's discretion, would compromise the participant's safety and cooperation in the trial.

About Anrs, Emerging Infectious Diseases

ANRS, the French National Agency for Research on AIDS and Viral Hepatitis, is a prominent research organization dedicated to advancing scientific knowledge and public health responses to emerging infectious diseases. With a focus on enhancing understanding, prevention, and treatment of viral infections, ANRS conducts and supports innovative clinical trials that address urgent health challenges. By fostering collaboration among researchers, healthcare professionals, and institutions, ANRS aims to translate research findings into effective strategies that improve patient outcomes and inform public health policies. Their commitment to addressing the dynamic landscape of infectious diseases positions them as a leader in global health research.

Locations

Kinshasa, , Congo, The Democratic Republic Of The

Conakry, , Guinea

Monrovia, , Liberia

Freetown, , Sierra Leone

Patients applied

0 patients applied

Trial Officials

Placide MBALA, MD, MSPH, PhD

Study Chair

INRB

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported