Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

OBJECTIVES: When malaria vectors consume ivermectin in a blood meal, their survival probability decreases, potentially reducing malaria transmission during mass drug administrations (MDA). However, questions remain regarding the optimal dosing. This study aimed at comparing the mosquitocidal effect and pharmacokinetics of two dose regimens of ivermectin for malaria vector control. DESIGN: We conducted an open-label randomized control trial in Kenya staggered in blocks with sequential intervention groups and parallel controls. Participants were randomly assigned (2:1:1:1) using computer random sequence generation, unstratified, with one block of six pharmacokinetic only participants (single-dose ivermectin) and six blocks of four participants (3:1 intervention vs control), to receive single-dose ivermectin (400 mcg/kg, n=12), three daily doses (three-day regimen 300 mcg/kg, n=6), albendazole (400 mg, n=6), or no treatment (negative control, n=6).Our primary outcome was Anopheles gambiae survival (time-to-event (days)) post blood feeding up to 10-days after drug administration. We also evaluated pharmacokinetics (Cmax, AUC, Tmax, Thalf) up to 7 days post treatment. RESULTS: A total of 36 healthy volunteers aged 21-32 years were recruited into the study and followed up to completion with 2 participants not attending visit on day 28. All drug regimens were well tolerated. Both regimens showed significant mosquitocidal effect in the first 7 days. At 10-days post treatment single dose presented superior longevity of effect (aHR(adjusted hazard ratio)=3.91; 95% CI=1.93- 7.93; p<0.001) compared to triple dose (aHR=1.79; 95% CI=0.88-3.62; p=0.0.11). Albendazole had overall no mosquitocidal effect. CONCLUSIONS: It is unclear why a single dose led to increased bio-efficacy compared to triple dose. We recommend trials investigating ivermectin MDA for malaria control to consider single-dose ivermectin. A single-dose regimen is also expected to present additional operational advantages compared to a three-day regimen leading to improved programmatic suitability.

Original publication

DOI

10.1016/j.ijid.2024.107236

Type

Journal article

Journal

Int J Infect Dis

Publication Date

06/09/2024

Keywords

Anopheles gambiae, endectocides, ivermectin, malaria, pharmacokinetics, vector control