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Single‑Dose Pharmacokinetics and Safety of the Oral Galectin‑3 Inhibitor, Selvigaltin (GB1211), in Participants with Hepatic Impairment.

Authors :
Aslanis V
Gray M
Slack RJ
Zetterberg FR
Tonev D
Phung
Smith B
Jacoby B
Schambye H
Krastev Z
Ungell AL
Lindmark B
Source :
Clinical drug investigation [Clin Drug Investig] 2024 Oct; Vol. 44 (10), pp. 773-787. Date of Electronic Publication: 2024 Oct 02.
Publication Year :
2024

Abstract

Background and Objectives: Selvigaltin (GB1211), an orally available small molecule galectin-3 inhibitor developed as a treatment for liver fibrosis and cirrhosis, was evaluated to assess the effect of hepatic impairment on its pharmacokinetics and safety to address regulatory requirements.<br />Methods: GULLIVER-2 was a Phase Ib/IIa three-part study. Parts 1 and 3 had single-dose, open-label designs assessing pharmacokinetics (plasma [total and unbound] and urine), safety, and tolerability of 100 mg oral selvigaltin in participants with moderate (Child-Pugh B, Part 1) or severe (Child-Pugh C, Part 3) hepatic impairment, compared with healthy-matched participants (n = 6 each).<br />Results: All participants received selvigaltin and completed the study. No adverse events were reported. The median time to reach maximum total plasma concentration following drug administration was of 3.49 and 4.00 h post-dose for Child-Pugh B and C participants, respectively; comparable with controls. Total plasma exposure was higher for participants with hepatic impairment compared with controls. Whilst maximum plasma concentration (C <subscript>max</subscript> ) was unaffected in Child-Pugh B participants, area under the plasma concentration-time curve from time zero to infinity (AUC <subscript>∞</subscript> ) increased by ~ 1.7-fold compared with controls, and half-life was prolonged (geometric mean 28.15 vs 16.38 h). In Child-Pugh C participants, C <subscript>max</subscript> increased by ~ 1.3-fold, AUC <subscript>∞</subscript> increased by ~ 1.5-fold, and half-life was prolonged (21.05 vs 16.14 h). No trend was observed in plasma unbound fractions or urinary excretion of unchanged selvigaltin in either group.<br />Conclusion: Hepatic impairment increased selvigaltin exposure without safety concerns. These data can inform dose recommendations for future clinical programmes.<br />Trial Registration: Clinicaltrials.gov NCT05009680.<br /> (© 2024. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)

Details

Language :
English
ISSN :
1179-1918
Volume :
44
Issue :
10
Database :
MEDLINE
Journal :
Clinical drug investigation
Publication Type :
Academic Journal
Accession number :
39358661
Full Text :
https://doi.org/10.1007/s40261-024-01395-7