Novel Patient‐Friendly Orodispersible Formulation of Ivermectin is Associated With Enhanced Palatability, Controlled Absorption, and Less Variability: High Potential for Pediatric Use

Author:

Dao Kim1,Buettcher Michael234ORCID,Golhen Klervi2,Kost Jonas5ORCID,Schittny Andreas5ORCID,Duthaler Urs67,Atkinson Andrew28,Haefliger David1,Guidi Monia19ORCID,Bardinet Carine1,Chtioui Haithem1,Boulekbache Abdelwahab1,Buclin Thierry1ORCID,Huwyler Jörg5ORCID,Pfister Marc2ORCID,Rothuizen Laura E.1

Affiliation:

1. Clinical Pharmacology Service Lausanne University Hospital and University of Lausanne Lausanne Switzerland

2. Pediatric Pharmacology and Pharmacometrics Research Center University Children's Hospital Basel (UKBB) Basel Switzerland

3. Pediatric Infectious Diseases Children's Hospital of Central Switzerland (KidZ) Lucerne Switzerland

4. Faculty of Health Sciences and Medicine University of Lucerne Lucerne Switzerland

5. Department of Pharmaceutical Sciences Division of Pharmaceutical Technology University of Basel Basel Switzerland

6. Division of Clinical Pharmacology & Toxicology Department of Biomedicine University and University Hospital Basel Basel Switzerland

7. Division of Clinical Pharmacology & Toxicology Department of Pharmaceutical Sciences University of Basel Basel Switzerland

8. Division of Infectious Diseases Washington University in St. Louis School of Medicine St. Louis MO USA

9. Center for Research and Innovation in Clinical Pharmaceutical Sciences Lausanne University Hospital and University of Lausanne Lausanne Switzerland

Abstract

AbstractIvermectin has been used since the 1980s as an anthelmintic and antiectoparasite agent worldwide. Currently, the only available oral formulation is tablets designed for adult patients. A patient‐friendly orodispersible tablet formulation designed for pediatric use (CHILD‐IVITAB) has been developed and is entering early phase clinical trials. To inform the pediatric program of CHILD‐IVITAB, 16 healthy adults were enrolled in a phase I, single‐center, open‐label, randomized, 2‐period, crossover, single‐dose trial which aimed to compare palatability, tolerability, and bioavailability and pharmacokinetics of CHILD‐IVITAB and their variability against the marketed ivermectin tablets (STROMECTOL) at a single dose of 12 mg in a fasting state. Palatability with CHILD‐IVITAB was considerably enhanced as compared to STROMECTOL. Both ivermectin formulations were well tolerated and safe. Relative bioavailability of CHILD‐IVITAB compared to STROMECTOL was estimated as the ratios of geometric means for Cmax, AUC 0‐∞, and AUC0‐last, which were 1.52 [90% CI: 1.13‐2.04], 1.27 [0.99‐1.62], and 1.29 [1.00‐1.66], respectively. Maximum drug concentrations occurred earlier with the CHILD‐IVITAB formulation, with a median Tmax at 3.0 h [range 2.0‐4.0 h] versus 4.0 h [range 2.0‐5.0 h] with STROMECTOL (P = .004). With CHILD‐IVITAB, variability in exposure was cut in half (coefficient of variation: 37% vs 70%) compared to STROMECTOL. Consistent with a more controlled absorption process, CHILD‐IVITAB was associated with reduced variability in drug exposure as compared to STROMECTOL. Together with a favorable palatability and tolerability profile, these findings motivate for further clinical studies to evaluate benefits of such a patient‐friendly ODT formulation in pediatric patients with a parasitic disease, including infants and young children <15 kg.

Publisher

Wiley

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