Pharmacokinetics of Generic Pediatric Dolutegravir Dispersible Tablet in Thai Young Children Living With HIV Weighing Below Twenty Kilograms

Author:

Rungsapphaiboon Athiporn12,Wacharachaisurapol Noppadol34,Anugulruengkitt Suvaporn13ORCID,Sirikutt Pugpen5ORCID,Phasomsap Chayapa3ORCID,Tawan Monta3ORCID,Saisaengjan Chutima3ORCID,Na Nakorn Yossawadee5,Paiboon Nantika1ORCID,Songtaweesin Wipaporn Natalie13,Tawon Yardpiroon6,Cressey Tim R.6,Puthanakit Thanyawee13ORCID,

Affiliation:

1. From the Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand

2. Department of Pediatrics, Khon Kaen Hospital, Khon Kaen, Thailand

3. Center of Excellence for Pediatric Infectious Diseases and Vaccines, Faculty of Medicine, Chulalongkorn University

4. Department of Pharmacology, Center of Excellence in Clinical Pharmacokinetics and Pharmacogenomics, Faculty of Medicine, Chulalongkorn University

5. Department of Pediatrics, Queen Sirikit National Institute of Child Health, Bangkok, Thailand

6. PK Laboratory Department, AMS-PHPT Research Collaboration, Faculty of Associated Medical Science, Chiang Mai University, Chiang Mai, Thailand.

Abstract

Introduction: Dolutegravir (DTG) dispersible tablet (DTG-DT) is a pediatric-friendly formulation. We aimed to describe the pharmacokinetics and virologic responses of generic DTG-DT in children weighing <20 kg. Methods: Children living with HIV-1 and <7 years of age weighing 6 to <20 kg were eligible. A generic 10-mg scored DTG-DT was administered to children using 3 weight bands (WB): WB1 (6 to <10 kg), WB2 (10 to <14 kg) and WB3 (14 to <20 kg), at doses of 20 mg (higher than World Health Organization recommendation of 15 mg), 20 mg and 25 mg, respectively. Steady-state intensive pharmacokinetics (PK) was performed in fasting condition with blood sampling at predose and 1, 2, 3, 4, 6 and 24 hours postdose. DTG PK parameters were estimated using a noncompartmental analysis, and DTG trough concentrations (C24) and 24-hour area under the concentration-time curve were calculated. Comparisons were made with ODYSSEY and IMPAACT 2019. And 90% effective concentration of 0.32 mg/L was used as a reference individual DTG C24 concentration. Results: From August 2021 to March 2023, 29 Thai children with a median (interquartile range) age of 3.2 (1.5–4.8) years were enrolled; 8 in WB1, 9 in WB2 and 12 in WB3. All children were treatment experienced and 59% had HIV RNA <200 copies/mL. Overall geometric mean (coefficient of variation percentage) DTG C24 was 1.0 (46%) mg/L [WB1, 0.9 (53%); WB2, 0.9 (27%); WB3, 1.2 (51%)]. Geometric mean (coefficient of variation percentage) 24-hour area under the concentration-time curve was 83.2 (24%) mg h/L [WB1, 84.3 (31%); WB2, 76.9 (16%); WB3, 87.6 (25%)]. At weeks 24 and 48, 90% and 92% of participants had plasma HIV RNA <200 copies/mL. Conclusions: Generic DTG-DT provided adequate drug exposure in children weighing 6 to <20 kg. The exploratory dose of DTG 20 mg for children weighing 6 to <10 kg showed similar PK parameters to World Health Organization doses in the other WB.

Funder

Ratchadapiseksompotch Fund, Faculty of Medicine, Chulalongkorn University

Research Fund for HIV in Children and Youth, Faculty of Medicine, Chulalongkorn University

Publisher

Ovid Technologies (Wolters Kluwer Health)

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