Mass Vaccine and Drug Administration, Bangladesh
Recruiting now · Phase 4
Conditions studied: Plasmodium Falciparum Malaria
In brief
This is an open i.e. not blinded, cluster-randomised, controlled intervention study. The study will use a factorial design to estimate the protective effectiveness of mass drug administrations, mass vaccinations, combined mass vaccinations and drug administrations versus the current standard of care.
Key facts
- Study ID
- NCT06068530
- Run by
- University of Oxford
- People needed
- 10000
- Starts
- 2025-02-15
- Expected to finish
- 2028-02-01
- Last updated by the study team
- 2025-12-18
Who can join
Age: 1 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Current residence in a study village irrespective of permanence
- Age 6 months and above (no upper age limit)
- Written informed consent provided by participants (or a parent/guardian in case the participant is under 18 years old)
You may not qualify if…
- Pregnancy, plan to get pregnant, or breastfeeding.
- Acute illness requiring intervention
- A history of an adverse reaction to study drugs/vaccine and prior receipt of any other malaria vaccine or enrolment in another intervention trial.
Where it is running
- Alikadam Upazila Health Complex — Bāndarban, Bangladesh (enrolling)
- Lama Upazila Health Complex — Lāma, Bangladesh (enrolling)
Full record on ClinicalTrials.gov
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