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Trial · NCT05252845

Registered outcomes25

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryOccurrence of Unsolicited Adverse Events (AEs), According to the Medical Dictionary for Regulatory Activities (MedRA) Classification.From the date of the first vaccination to 28 days after the last vaccination (up to approximately 1 month)
PrimaryOccurrence of Serious Adverse Events (SAEs), According to the MedRA Classification.During the whole study period, i.e. during a 6-month follow-up period from the receipt of first vaccination
PrimaryOccurrence of Solicited Adverse Event Within 7 Days of Each VaccinationWithin 7 days of each vaccination.
SecondaryNumber of Participants With Seroconversions in C-Termat study Month 1Number of Participants with Seroconversions in C-Term
SecondaryNumber of Participants With Seroconversions in C-Termat study Month 2Number of Participants with Seroconversions in C-Term
SecondaryNumber of Participants With Seroconversions in C-Termat study Month 3Number of Participants with Seroconversions in C-Term
SecondaryNumber of Participants With Seroconversions in C-Termat study Month 6Number of Participants with Seroconversions in C-Term
SecondaryNumber of Participants With Seroconversions in NANPat study Month 1Number of Participants with Seroconversions in NANP
SecondaryNumber of Participants With Seroconversions in NANPat study Month2Number of Participants with Seroconversions in NANP
SecondaryNumber of Participants With Seroconversions in NANPat study Month 3Number of Participants with Seroconversions in NANP
SecondaryNumber of Participants With Seroconversions in NANPat study Month 6Number of Participants with Seroconversions in NANP
SecondaryNumber of Participants With Seroconversions in R21at study Month 1Number of Participants with Seroconversions in R21
SecondaryNumber of Participants With Seroconversions in R21at study Month 2Number of Participants with Seroconversions in R21
SecondaryNumber of Participants With Seroconversions in R21at study Month 3Number of Participants with Seroconversions in R21
SecondaryNumber of Participants With Seroconversions in R21at study Month 6Number of Participants With Seroconversions in R21
SecondaryNumber of Participants With Seroconversions in HBsAgat study Month 1Number of Participants with Seroconversions in HBsAg
SecondaryNumber of Participants With Seroconversions in HBsAgat study Month 2Number of Participants with Seroconversions in HBsAg
SecondaryNumber of Participants With Seroconversions in HBsAgat study Month 3Number of Participants with Seroconversions in HBsAg
SecondaryNumber of Participants With Seroconversions in HBsAgat study Month 6Number of Participants with Seroconversions in HBsAg
SecondaryFor Arms 1 and 3, Piperaquine Levels Following the Administration of the Antimalarials With or Without VaccineStudy month 0For Arms 1 and 3, Piperaquine levels (Cmax) following the administration of the antimalarials with or without vaccine

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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