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VAC-SIP-YF (Vaccination- Safety & Immunogenicity During Pregnancy- Yellow Fever)

Study acronym: VAC-SIP-YF
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Re-verified, no change to tracked fieldsv4
  2. Trial status: Not Yet Recruiting to Recruitingv3 Show 4 more changesShow less
    • Primary completion date: Dec 2027 to Mar 2028
    • Study completion date: Dec 2029 to Mar 2030
    • Start date changed from estimate of Dec 2024 to Mar 24, 2025
    • Site details revised
  3. Primary completion date: Nov 2027 to Dec 2027
    • Study completion date: Nov 2029 to Dec 2029
    • Start date: Nov 2024 to Dec 2024
    v2
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The aim of this study is to compare the immunogenicity induced by yellow fever vaccination administered during pregnancy with that induced by vaccination outside pregnancy, and to assess the maternal and fetal tolerance of this vaccination.
Trial Details
NCT Number NCT06694766
Lead Sponsor Institut Pasteur
Collaborators: Cerballiance
Conditions
(from sponsor)		 Yellow Fever Vaccine
Enrollment 270 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov