Back to Search Start Over

A pilot study of golexanolone, a new GABA-A receptor-modulating steroid antagonist, in patients with covert hepatic encephalopathy

Authors :
Montagnese, Sara
Lauridsen, Mette
Vilstrup, Hendrik
Zarantonello, Lisa
Lakner, Geza
Fitilev, Sergey
Zupanets, Igor
Kozlova, Irina
Bunkova, Elena
Tomasiewicz, Krzysztof
Berglund, Jan Erik
Rorsman, Fredrik
Hagström, Hannes
Kechagias, Stergios
Ocklind, Carin Edmark
Mauney, Joe
Thunarf, Fredrik
Mokhatarani, Masoud
Bäckström, Torbjörn
Doverskog, Magnus
Lins, Lars-Erik
Månsson, Maria
Samuelson, Per
Nilsson, Dag
Schalling, Martin
Johansson, Maja
Arlander, Eva
Scharschmidt, Bruce F.
Montagnese, Sara
Lauridsen, Mette
Vilstrup, Hendrik
Zarantonello, Lisa
Lakner, Geza
Fitilev, Sergey
Zupanets, Igor
Kozlova, Irina
Bunkova, Elena
Tomasiewicz, Krzysztof
Berglund, Jan Erik
Rorsman, Fredrik
Hagström, Hannes
Kechagias, Stergios
Ocklind, Carin Edmark
Mauney, Joe
Thunarf, Fredrik
Mokhatarani, Masoud
Bäckström, Torbjörn
Doverskog, Magnus
Lins, Lars-Erik
Månsson, Maria
Samuelson, Per
Nilsson, Dag
Schalling, Martin
Johansson, Maja
Arlander, Eva
Scharschmidt, Bruce F.
Publication Year :
2021

Abstract

Background & Aims: Golexanolone is a novel small molecule GABA-A receptor-modulating steroid antagonist under development for the treatment of cognitive and vigilance disorders caused by allosteric over-activation of GABA-A receptors by neurosteroids. It restored spatial learning and motor coordination in animal models of hepatic encephalopathy (HE) and mitigated the effects of intravenous allopregnanolone in healthy adults in a dose-dependent fashion. Herein, we report data on the safety, pharmacokinetics (PK) and efficacy of golexanolone in adult patients with cirrhosis. Methods: Following single/multiple ascending dose studies, adults with Child-Pugh A/B cirrhosis and abnormal continuous reaction time (CRT) on screening were randomized to 3 weeks dosing with golexanolone (10, 40 or 80 mg BID) or placebo. CRT, psychometric hepatic encephalopathy score (PHES), animal naming test (ANT), Epworth sleepiness scale (ESS) and electroencephalogram (mean dominant frequency [MDF]; delta+theta/alpha+beta ratio [DT/AB]) were obtained at baseline, 10, and 21 days. Results: Golexanolone exhibited satisfactory safety and PK. Baseline characteristics were similar between the 12 and 33 patients randomized to placebo or golexanolone, respectively. By prespecified analyses, golexanolone was associated with directionally favourable changes vs. placebo in ESS (p = 0.047), MDF (p = 0.142) and DT/AB (p = 0.021). All patients also showed directionally favourable changes in CRT, PHES and ANT, but with no statistical difference between golexanolone and placebo. Post hoc analyses taking into account the variability and improvement in CRT, PHES and ANT observed between screening and baseline suggested an efficacy signal by cognitive measures as well. Conclusion: Golexanolone was well tolerated and associated with improvement in cognitive performance. These results implicate GABA-A receptor-modulating neurosteroids in the pathogenesis of HE and support the therapeutic potential of golexan<br />Funding Agencies|Umecrine Cognition AB

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1269610158
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1016.j.jhep.2021.03.012