Active, not recruitingPHASE1, PHASE2NCT06549257
Assessing the Safety, Immunogenicity and Ex-vivo Efficacy of Two Candidate Malaria Transmission Blocking Vaccines, Pfs25-IMX313 and Pfs45/48 Administered Alone and in Combination, in Matrix-M Adjuvant
Studying Malaria
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University of Oxford
- Principal Investigator
- Paola Cicconi, PhDUniversity of Oxford
- Intervention
- Pfs25-IMX313, Pfs48/45(biological)
- Enrollment
- 56 target
- Eligibility
- 5-45 years · All sexes
- Timeline
- 2025 – 2026
Study locations (1)
- Institut des Sciences et Techniques (INSTech), Bobo-Dioulasso, Burkina Faso
Collaborators
European and Developing Countries Clinical Trials Partnership (EDCTP)
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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