Evidence based optimal dosing of intravenous artesunate in children with severe falciparum malaria

Journal article

The majority of deaths from malaria are in young African children. Parenteral artesunate (ARS) is the first-line treatment for severe falciparum malaria. Since 2015, the World Health Organization has recommended individual doses of 3 mg/kg for children weighing < 20 kg. Recently, the US Food and Drug Administration (FDA) has challenged this recommendation, based on a simulated pediatric population, and argued for a lower dose in younger children (2.4 mg/kg). In this study, we performed population pharmacokinetic (PK) modeling of plasma concentration data from 80 children with severe falciparum malaria in the Democratic Republic of Congo who were given 2.4 mg/kg of ARS intravenously. Bayesian hierarchical modeling and a two-compartment parent drug-metabolite PK model for ARS were used to describe the population PKs of ARS and its main biologically active metabolite dihydroartemisinin. We then generated a virtual population representative of the target population in which the drug is used and simulated the total first-dose exposures. Our study shows that the majority of younger children given the lower 2.4 mg/kg dose of intravenous ARS do not reach the same drug exposures as older children above 20 kg. This finding supports withdrawal of the FDA's recent lower ARS dose recommendation as parenteral ARS is an extremely safe and well-tolerated drug and there is potential for harm from underdosing in this rapidly lethal infection.

Authors: Haghiri, A; Price, DJ; Fitzpatrick, P; Dini, S; Rajasekhar, M

• Publication status: Published
• Peer review status: Peer reviewed
• Publisher: Wiley
• Journal: Clinical Pharmacology and Therapeutics
• Publication date: 2023-09-15
• Acceptance date: 2023-08-26
• DOI: 10.1002/cpt.3041
• EISSN: 1532-6535
• ISSN: 0009-9236
• Pmid: 37666798
• Language: English
• Keywords: pharmaceuticals; pediatric; vector-borne diseases; rare diseases; biomedical and clinical sciences; medical microbiology; good health and well being; infectious diseases; malaria; infection; development of treatments and therapeutic interventions; FFR; clinical sciences; clinical research; evaluation of treatments and therapeutic interventions; orphan drug