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An Open Label, Randomized, Multicenter Study of Elafibranor in Children With Nonalcoholic Steatohepatitis.

Authors :
Goyal NP
Mencin A
Newton KP
Durelle J
Carrier C
Ugalde-Nicalo P
Noel B
Mouton J
Vargas D
Magrez D
Tadde B
Birman P
Best BM
Addy C
Schwimmer JB
Source :
Journal of pediatric gastroenterology and nutrition [J Pediatr Gastroenterol Nutr] 2023 Aug 01; Vol. 77 (2), pp. 160-165. Date of Electronic Publication: 2023 Apr 21.
Publication Year :
2023

Abstract

Objectives: Nonalcoholic fatty liver disease is the most common chronic liver disease in children. Elafibranor, a dual peroxisome proliferator-activated receptor α/δ agonist, has been proposed as a treatment for nonalcoholic steatohepatitis (NASH). The aims were to (1) describe pharmacokinetics (PK), safety, and tolerability of oral elafibranor at 2 doses (80 and 120 mg) in children 8-17 years and (2) assess changes in aminotransferases.<br />Methods: Children with NASH were randomized to open-label elafibranor 80 mg or 120 mg daily for 12 weeks. The intent-to-treat analysis included all participants who received at least 1 dose. Standard descriptive statistics and PK analyses were performed.<br />Results: Ten males [mean 15.1 years, standard deviation (SD) 2.2] with NASH were randomized to 80 mg (n = 5) or 120 mg (n = 5). Baseline mean alanine aminotransferase (ALT) was 82 U/L (SD 13) and 87 U/L (SD 20) for 80 mg and 120 mg groups, respectively. Elafibranor was rapidly absorbed and well tolerated. Elafibranor plasma exposure increased between the 80 mg and 120 mg dose with a 1.9- and 1.3-fold increase in median Cmax and AUC 0-24 , respectively. End of treatment mean ALT was 52 U/L (SD 20) for the 120 mg group, with a relative mean ALT change from baseline of -37.4% (SD 23.8%) at 12 weeks.<br />Conclusions: Once daily dosing of elafibranor was well tolerated in children with NASH. There was a 37.4% relative reduction from mean baseline ALT in the 120 mg group. Decreasing ALT may be associated with improvement in liver histology, thus could be considered a surrogate for histology in early phase trials. These results may support further exploration of elafibranor in children with NASH.<br />Competing Interests: B.N. and D.M. are shareholders of GENFIT. J.B.S. reports grants to UCSD from Intercept and Seraphina outside the submitted work. The remaining authors report no conflicts of interest.<br /> (Copyright © 2023 by European Society for European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition.)

Details

Language :
English
ISSN :
1536-4801
Volume :
77
Issue :
2
Database :
MEDLINE
Journal :
Journal of pediatric gastroenterology and nutrition
Publication Type :
Academic Journal
Accession number :
37084342
Full Text :
https://doi.org/10.1097/MPG.0000000000003796