The purpose of this study is: a) to assess adverse maternal/fetal outcomes in pregnant women randomized to receive the 2- dose Ebola vaccine regimen (Ad26.ZEBOV, MVA-BN-Filo \[Group A\]) and in control women (unvaccinated pregnant women \[Group B\]); and b) to assess adverse neonatal/infant outcomes in neonates/infants born to women randomized to receive the 2-dose Ebola vaccine regimen (Ad26.ZEBOV, MVA-BN-Filo \[Group A\]) and in neonates/infants born to control women (unvaccinated during pregnancy \[Group B\]).
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Percentage of Participants with Maternal Deaths
Timeframe: Up to 6 weeks post-completion/termination of pregnancy
Percentage of Participants with Spontaneous Abortion
Timeframe: Up to 6 weeks post-completion/termination of pregnancy
Percentage of Participants with Stillbirth
Timeframe: Up to 6 weeks post-completion/termination of pregnancy
Percentage of Participants on the Pathways to Preterm Birth
Timeframe: Up to 6 weeks post-completion/termination of pregnancy
Percentage of Participants with Pre-eclampsia/ eclampsia
Timeframe: Up to 6 weeks post-completion/termination of pregnancy
Percentage of Participants with Antenatal Bleeding
Timeframe: Up to 6 weeks post-completion/termination of pregnancy
Percentage of Participants with Postpartum Hemorrhage
Timeframe: Up to 6 weeks post-completion/termination of pregnancy
Percentage of Newborns with Major Congenital Malformations born to Participants
Timeframe: At birth
Percentage of Newborns Small for Gestational age (SGA) born to Participants
Timeframe: At birth
Percentage of Newborns with Low Birth Weight born to Participants
Timeframe: At birth
Percentage of Newborns with Preterm Birth born to Participants
Timeframe: At birth
Percentage of Neonatal Deaths in Neonates Born to Participants
Timeframe: Up to 28 days
Percentage of Infants (of Participants) who Fail to Thrive
Timeframe: From birth up to 14 weeks of age