Clinical trial

Enhancing Immunity to Malaria in Young Children With Effective Chemoprevention

Name
MIC-DroP
Description
The MIC-DroP trial will test the hypothesis that preventing early life blood-stage malaria antigenic exposure with intermittent preventive therapy (IPT) enhances protective immunity to malaria. This study will take advantage of a unique opportunity to study infants born to mothers followed in a NIH-funded randomized controlled trial of novel intermittent preventive therapy in pregnancy (IPTp) regimens (NCT04336189). MIC-DroP will leverage the parent IPTp study to enroll 924 children who will be randomized at 8 weeks of age to receive no intermittent preventive therapy in childhood (IPTc), monthly DP from 8 weeks to 1 year of age, or monthly DP from 8 weeks to 2 years of age, and then follow children to 4 years of age. The primary outcome of this study will be to compare the incidence of malaria from 2 to 4 years of age among children randomized to receive no IPTc, monthly DP for the first year of life, or monthly DP for the first two years of life. Investigators will also leverage this trial to evaluate immune development during early childhood.
Trial arms
Trial start
2022-02-08
Estimated PCD
2026-08-31
Trial end
2026-08-31
Status
Active (not recruiting)
Phase
Early phase I
Treatment
Dihydroartemisinin-piperaquine (DP)
Duo-Cotecxin 20mg/160mg tabs by Holley-Cotec, Beijing, China Each treatment with DP will consist of half-strength tablets given once a day for 3 consecutive days according to weight-based guidelines.
Arms:
IPTc DP 1 year, IPTc DP 2 years
Other names:
Duo-Cotecxin
DP Placebo
Placebos will be identical appearance to DP.
Arms:
IPTc DP 1 year, No IPTc
Size
924
Primary endpoint
Incidence of symptomatic malaria following cessation of IPTc
2 years to 4 years of age
Eligibility criteria
Inclusion Criteria: 1. Born to HIV-uninfected mother enrolled in parent clinical trial of intermittent preventative treatment of malaria in pregnancy (IPTp-SP vs. IPTp-DP vs. IPTp-SP+DP, NCT 04336189) 2. Resident of Busia District 3. Provision of informed consent by parent/guardian 4. Agreement to present for any illness and avoid, where possible, medications outside the study protocol. Exclusion Criteria: 1. Intention of moving outside Busia district during the study period 2. Active medical problem requiring in-patient evaluation or chronic medical condition requiring frequent medical attention
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE3'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'SEQUENTIAL', 'interventionModelDescription': 'Double blinded randomized controlled trial', 'primaryPurpose': 'PREVENTION', 'maskingInfo': {'masking': 'TRIPLE', 'maskingDescription': "Administration of all study drugs will be double blinded. All doses of study drugs will be prepackaged by a study pharmacist and administered by a study nurse blinded to the study participant's treatment regimen. All 3 daily doses will be directly observed in the clinic. If a study participant vomits the study drug within 30 minutes of administration, the drug will be re-administered. All doses of study drugs will be given between 8 and 104 weeks (2 years) of age.", 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR']}}, 'enrollmentInfo': {'count': 924, 'type': 'ACTUAL'}}
Updated at
2024-03-08

1 organization

1 product

1 indication

Indication
Malaria