Evaluation of sunobinop for next-day residual effects in healthy participants

• Published in: Frontiers in pharmacology Vol. 15; p. 1432902
• Main Authors: Cipriano, Alessandra, Kapil, Ram P, Zhou, Mingyan, Shet, Manjunath S, Harris, Stephen C, Apseloff, Glen, Whiteside, Garth T
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 19.08.2024
• Subjects: healthy participants; insomnia; next-day residual effects; nociceptin/orphanin FQ; Pharmacology; sunobinop; sunobinop; nociceptin/orphanin FQ; healthy participants; next-day residual effects; insomnia
• ISSN: 1663-9812; 1663-9812
• DOI: 10.3389/fphar.2024.1432902

Sunobinop is a novel, potent, selective partial agonist at nociceptin/orphanin FQ peptide (NOP) receptors. The primary objective of this randomized, double-blind, placebo-controlled study was to assess the next-day residual effects of an evening dose of sunobinop in healthy participants. Participants were randomized into 1 of 5 treatment sequences. Treatment consisted of 1 dose each of sunobinop 0.2, 0.6, 2, and 6 mg suspension and placebo suspension. Key pharmacodynamic (PD) measures included the digit symbol substitution test (DSST), Karolinska sleepiness scale (KSS), and body sway. The randomized safety population consisted of 25 participants. The DSST, KSS, and body sway showed dose-dependent effects following the administration of sunobinop, with no significant differences versus placebo at sunobinop doses <2 mg. At sunobinop 2 mg, PD effects were relatively small in magnitude and inconsistent. The last timepoint where significant differences between sunobinop 2 mg and placebo on the DSST, KSS, and body sway were observed was at 12 h, 16.5 h, and 13.5 h postdose, respectively. Sunobinop 6 mg resulted in larger and consistent PD effects, with significant differences from placebo at all timepoints up to 16.5-18 h postdose. Somnolence was the most frequently reported adverse event (AE), and all AEs were mild-to-moderate. No deaths occurred during the study or discontinuations due to an AE. Overall, a nighttime oral dose of sunobinop up to 2 mg was safe and generally well tolerated in healthy participants with limited next-day residual effects that were consistent with other sedative/hypnotic drugs.