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Single- and Multiple-Dose Safety, Tolerability, and Pharmacokinetic Profiles of ASP8062: Results From 2 Phase 1 Studies.

Authors :
Walzer M
Marek GJ
Wu R
Nagata M
Han D
Source :
Clinical pharmacology in drug development [Clin Pharmacol Drug Dev] 2020 Apr; Vol. 9 (3), pp. 297-306. Date of Electronic Publication: 2020 Jan 11.
Publication Year :
2020

Abstract

ASP8062 is an orally active γ-amino-butyric acid type B (GABA <subscript>B</subscript> ) receptor positive allosteric modulator currently in phase 2 development. Safety and pharmacokinetic (PK) profiles of ASP8062 were evaluated in 2 studies in healthy subjects. The first study (a first-in-human study) evaluated single ascending doses (SAD) of ASP8062. The second study was composed of 2 parts: part 1 evaluated multiple ascending doses (MAD) of ASP8062 for 14 days, and part 2 was a single-dose arm to assess the PK of ASP8062 in cerebrospinal fluid (CSF). Fifty-six men (SAD) and 56 subjects (24 women and 32 men; MAD) were enrolled. Across the SAD dosing range, area under the concentration-time curve was dose proportional; increases in maximum plasma concentration appeared linear but were slightly less than dose proportional. Time to maximal concentration and half-life were 1-4 hours and ∼40-50 hours, respectively; no food effect was observed. ASP8062 PK properties at steady state were similar to those following a single dose. Steady state was achieved by ∼day 9 with ∼2-fold accumulation, and ASP8062 was detected in CSF. ASP8062 was well tolerated; no clear evidence of ASP8062's effects on safety, cognition, drug withdrawal, or suicidal ideation/behavior was observed. These data support the development of ASP8062 in indications where the GABA <subscript>B</subscript> receptor is a target.<br /> (© 2020, The American College of Clinical Pharmacology.)

Details

Language :
English
ISSN :
2160-7648
Volume :
9
Issue :
3
Database :
MEDLINE
Journal :
Clinical pharmacology in drug development
Publication Type :
Academic Journal
Accession number :
31926000
Full Text :
https://doi.org/10.1002/cpdd.766