Ad26.ZEBOV
Sponsors
Crucell Holland BV, Janssen Vaccines & Prevention B.V., University of Oxford, National Institute of Allergy and Infectious Diseases (NIAID), London School of Hygiene and Tropical Medicine
Conditions
EbolaEbola Viral DiseaseEbola Virus DiseaseHealthyHemorrhagic Fever, EbolaHiv
Phase 1
A Study to Assess the Safety and Immunogenicity of Heterologous Prime-Boost Ebola Vaccine Regimens in Healthy Participants
CompletedNCT02376400
Start: 2015-04-30End: 2016-09-30Updated: 2016-12-08
A Study to Evaluate the Safety and Immunogenicity of Heterologous Prime-Boost Ebola Vaccine Regimens in Healthy Participants
CompletedNCT02376426
Start: 2015-03-31End: 2016-06-30Updated: 2016-12-08
A Study to Assess Ebola Vaccines ChAd3-EBO-Z and Ad26.ZEBOV
CompletedNCT02495246
Start: 2015-09-21End: 2017-08-22Updated: 2018-04-11
A Study to Evaluate Safety, Tolerability, and Immunogenicity of Heterologous Prime-boost Regimens Using the Multivalent Filovirus Vaccines Ad26.Filo and MVA-BN-Filo Administered in Different Sequences and Schedules in Healthy Adults
CompletedNCT02860650
Start: 2016-08-31End: 2018-01-31Updated: 2018-02-05
Phase 2
A Study to Assess Safety, Tolerability, and Immunogenicity of Three Heterologus 2-dose Regimens of the Candidate Prophylactic Vaccines for Ebola in Healthy Adults
CompletedNCT02416453
Start: 2015-06-15End: 2018-01-19Updated: 2021-02-08
Safety, Tolerability and Immunogenicity Study of 3 Prime-boost Regimens for Ebola Vaccines Ad26.ZEBOV/MVA-BN-Filo in Healthy Adults, Children and Human Immunodeficiency Virus Positive (HIV+) Adults
CompletedNCT02564523
Start: 2015-11-06End: 2019-02-12Updated: 2022-03-07
Safety, Tolerability and Immunogenicity Study of 2-dose Heterologous Regimens for Ebola Vaccines Ad26.ZEBOV/MVA-BN-Filo
CompletedNCT02598388
Start: 2015-12-10End: 2018-12-12Updated: 2025-02-04
Partnership for Research on Ebola VACcinations
CompletedNCT02876328
Start: 2017-03-27End: 2023-12-20Updated: 2024-06-26
A Study of 2-dose Vaccination Regimen of Ad26.ZEBOV and MVA-BN-Filo in Infants
CompletedNCT03929757
Start: 2019-08-19End: 2022-09-28Updated: 2025-05-25
An open label, phase 2 study to evaluate the safety and immunogenicity of an Ad26.ZEBOV booster dose in Human Immunodeficiency Virus Positive (HIV+) adults previously vaccinated with the Ad26.ZEBOV, MVA-BN-Filo vaccine regimen
Active, not recruitingPACTR202102747294430
Start: 2021-03-15Target: 50Updated: 2026-01-27
Ad26.ZEBOV Booster in HIV+ Adults Previously Vaccinated With Ad26.ZEBOV/MVA-BN-Filo (EBOVAC HIV+ Booster Study)
CompletedNCT05064956
Start: 2021-10-06End: 2022-10-24Updated: 2023-02-21
Phase 3
Staged Phase 3 Study to Assess the Safety and Immunogenicity of Ebola Candidate Vaccines Ad26.ZEBOV and MVA-BN-Filo
CompletedNCT02509494
Start: 2015-09-30End: 2019-07-03Updated: 2022-07-18
Long-term Safety Follow-up of Participants Exposed to the Candidate Ebola Vaccines Ad26.ZEBOV and/or MVA-BN-Filo
TerminatedNCT02661464
Start: 2016-05-31End: 2021-12-13Updated: 2024-01-02
A Study of 2-dose Vaccine Regimen Using 3 Consecutive Lots of Ad26.ZEBOV and MVA-BN-Filo in Adult Participants
CompletedNCT04228783
Start: 2020-02-18End: 2022-04-25Updated: 2025-05-25
A Study of a 2-dose Ebola Vaccine Regimen of Ad26.ZEBOV Followed by MVA-BN-Filo in Healthy Pregnant Women
CompletedNCT04556526
Start: 2020-10-05End: 2023-03-02Updated: 2025-02-03
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