Sulfadoxine-pyrimethamine Plus Dihydroartemisinin-piperaquine for Intermittent Preventive Treatment in Pregnancy

Phase 3Active Not RecruitingNCT05426434

Menzies School of Health Research1,172 enrolled

Overview

This trial tests the hypothesis that intermittent preventive treatment in pregnancy (IPTp) with sulfadoxine-pyrimethamine (SP) plus dihydroartemisinin-piperaquine (DP) significantly reduces the risk of malaria infection (primary outcome) and adverse birth outcomes (key secondary outcome) in an endemic area of Papua New Guinea (PNG), compared to IPTp with SP alone (the current standard of care). To test this hypothesis a double-blinded, placebo-controlled, phase-III, superiority trial will individually randomize 1,172 HIV-uninfected pregnant women enrolled from 12-26 gestational weeks in equal proportions to one of two IPTp arms: 1) SP given every for weeks, or 2) SP+DP given every 4 weeks. DP placebos will be used to ensure adequate blinding is achieved in the study and follow-up will end 28 days after giving birth.

Plasmodium falciparum and P. vivax infections cause malaria, maternal anemia and interfere with the development of the fetus, thereby increasing the risks of adverse pregnancy outcomes such as miscarriage, stillbirth, premature birth, fetal growth restriction, low birth weight, and infant death. Infected pregnant women are frequently asymptomatic, and current point-of-care tests miss placental and low-density infections. Monthly intermittent preventive treatment in pregnancy (IPTp) with sulfadoxine-pyrimethamine (SP) is designed to clear asymptomatic infections and provide post-treatment prophylaxis. The World Health Organization recommends IPTp with SP and long-lasting insecticidal bed nets for the prevention of malaria in pregnancy in endemic areas of sub-Saharan Africa. However, the emergence and spread of high-grade parasite resistance to SP threatens to compromise this strategy. Dihydroartemisinin-piperaquine (DP) is a safe fixed-dose artemisinin-based combination therapy used for the management of uncomplicated P. falciparum and P. vivax malaria in pregnancy and has emerged as a potential candidate to replace SP for IPTp. In comparative trials conducted in high-transmission settings in sub-Saharan Africa IPTp with DP was safe and significantly reduced the risk of P. falciparum infection compared to IPTp with SP. IPTp with DP also reduced the risk of P. vivax parasitemia in Papua Indonesia when compared to a single screen and treat approach. However, DP's superior antimalarial efficacy in African studies did not translate to large reductions in adverse pregnancy outcomes in these trials. This suggests that SP, whilst failing as an antimalarial, may prevent adverse pregnancy events via potent non-malarial effects that are not inherent to DP. For example, SP may provide protection from pathogens other than malaria parasites that are directly or indirectly involved in the causation of adverse pregnancy outcomes. Papua New Guinea (PNG) is characterized by moderate intensity co-transmission of P. falciparum and P. vivax and a high burden of adverse pregnancy outcomes. PNG is the only country outside of Africa that has a policy of IPTp with SP. However, P. vivax resistance to SP is now common, high-grade P. falciparum resistance to SP may be emerging, and DP could provide enhanced antimalarial protection. However, given the high burden of adverse pregnancy outcomes from malaria- and non-malaria related causes, simply replacing SP with DP for IPTp in PNG may not lead to a reduction in adverse birth outcomes. Instead, combining DP with SP for IPTp has the potential to substantially improve health outcomes by reducing the risk of malaria infection whilst harnessing the non-malaria-related benefits of SP. A double-blinded randomized controlled clinical trial will (1) compare the risk of malaria infection among pregnant women randomized to receive monthly IPTp with SP vs. SP+DP; (2) compare the risk of adverse pregnancy outcomes among pregnant women randomized to receive monthly IPTp with SP vs. SP+DP; and (3) compare safety and tolerability of monthly IPTp with SP vs SP+DP. The findings of this trial may have important policy implications, and the evidence generated will inform practice for PNG and sub-Saharan Africa.

Eligibility

Sex: FEMALEMin age: 16 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Pregnant women between 12-26 weeks' gestation * 16 years of age or older * Viable singleton intrauterine pregnancy * Permanent resident of the study area * Willing to adhere to scheduled and unscheduled study visit procedures * Willing to birth in a study clinic or hospital * Able to provide written informed consent Exclusion Criteria: * Multiple pregnancy (i.e. twins/triplets) * Known heart ailment or other chronic medical condition requiring frequent hospital care * Active medical problem requiring inpatient evaluation at the time of screening * Severe malformations or non-viable pregnancy if observed by ultrasound * Antimalarial therapy in the prior two weeks * Unable to provide written informed consent * Known allergy or contraindication to any of the study drugs * Early or active labour * Known HIV-positive status

Outcomes

Primary Outcomes

Malaria infection in pregnancy

'Malaria infection in pregnancy' is a composite outcome, defined as one or more episode of P. falciparum and/or P. vivax infection, detected by microscopy and/or qPCR in peripheral blood or placental blood, or P. falciparum and/or P. vivax infection, detected as active infection on placental histology. The surveillance period will run from two weeks after the first dose of the first monthly treatment up until and including delivery (numerator) in women who attend at least one scheduled or unscheduled visit during the surveillance period (denominator). Proportion of women with 'malaria infection in pregnancy'

Time frame: Starting two weeks after initial dose until and including delivery

Secondary Outcomes

Adverse pregnancy outcome

Composite adverse birth outcome is defined as the occurrence of any of the following: * Spontaneous miscarriage: Fetal loss \<28 weeks of gestational age * Stillbirth: Infant born deceased at ≥28 weeks of gestational age * Low birth weight (LBW): Live birth with birth weight \<2,500 grams * Preterm birth (PTB): Live birth \<37 weeks gestational age * Small-for-gestational age (SGA): Live birth with birth weight-for-gestational-age \<10th percentile of the INTERGROWTH-21st reference * Neonatal death: Live birth with neonatal death within the first 28 days of life Prevalence of adverse pregnancy outcome

Time frame: Time of delivery up to 28 days postpartum

Clinical malaria during pregnancy

Incidence of new episodes of fever or history of fever plus positive RDT confirmed by microscopy and/or qPCR during pregnancy

Time frame: Starting two weeks after initial dose until and including delivery

Parasitemia during pregnancy

Proportion of samples with parasites detected in maternal peripheral blood samples by microscopy or qPCR

Time frame: Starting two weeks after initial dose until and including delivery

Composite placental malaria detected by microscopy, qPCR or by histology

Prevalence of placental parasites by microscopy, qPCR, or placental histology