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Trials / Completed

CompletedNCT02933931

Immune Durability After VSV-EBOV Vaccination

Long-term Immune Durability After Vaccination With the Vesicular Stomatitis Virus-vectored Zaire Ebola Candidate Vaccine (VSV-EBOV): a Prospective Observational Cohort Study

Status
Completed
Phase
Study type
Observational
Enrollment
95 (actual)
Sponsor
University Hospital, Geneva · Academic / Other
Sex
All
Age
18 Years – 68 Years
Healthy volunteers
Not accepted

Summary

This prospective observational cohort study will follow the roughly 100 adults who received the VSV-ZEBOV vaccine in the Geneva phase 1 randomized controlled trial in 2014-2015 in order to determine their long-term (5-year) immune response to vaccination.

Detailed description

Background: During the Ebola epidemic of 2014-5, there was no proven therapy or prevention available beyond horizontal infection control measures. After the Canadian government donated 800 vials of the vaccine candidate VSV-EBOV to World Health Organization (WHO), the University Hospitals of Geneva agreed to perform a WHO-coordinated phase I/II double-blind, placebo-controlled randomized trial to assess the candidate's safety and immunogenicity healthy adult volunteers. The doses of 10 E7 pfu and 5 x 10 E7 pfu were tested in 35 and 16 volunteers, respectively, before a safety-driven study hold in late 2014. At trial resumption in early 2015, the remaining volunteers (n=51) received 3 x 10 E5 pfu. Thirteen volunteers received placebo. Among vaccinees, early immune responses were impressive, even at the lowest dose of 3 x 10 E5 pfu, and persisted well up to 6 months (last time point assessed). The trial successfully ended 12 months after injection. This prospective observational study will assess immune durability in this group of vaccinees at yearly time points up to five years post-vaccination.

Conditions

Timeline

Start date
2016-11-01
Primary completion
2020-01-01
Completion
2020-01-01
First posted
2016-10-14
Last updated
2021-05-26

Source: ClinicalTrials.gov record NCT02933931. Inclusion in this directory is not an endorsement.