PET clinical study of novel antipsychotic LB-102 demonstrates unexpectedly prolonged dopamine receptor target engagement.

Autor: Wong DF; Mallinckrodt Institute of Radiology, and Department of Radiology, Washington University in Saint Louis, St. Louis, MO, USA. dfwong@wustl.edu.; Department of Psychiatry, Washington University in Saint Louis, St. Louis, MO, USA. dfwong@wustl.edu.; Department of Neurology, Washington University in Saint Louis, St. Louis, MO, USA. dfwong@wustl.edu.; Department of Neuroscience, Washington University in Saint Louis, St. Louis, MO, USA. dfwong@wustl.edu., Chand GB; Mallinckrodt Institute of Radiology, and Department of Radiology, Washington University in Saint Louis, St. Louis, MO, USA., Caito N; Mallinckrodt Institute of Radiology, and Department of Radiology, Washington University in Saint Louis, St. Louis, MO, USA., Eramo A; LB Pharmaceuticals Inc., New York, NY, USA., Grattan VT; LB Pharmaceuticals Inc., New York, NY, USA., Hixon MS; Mark S. Hixon Consulting LLC, San Diego, CA, USA., Nicol G; Department of Psychiatry, Washington University in Saint Louis, St. Louis, MO, USA., Lessie E; Mallinckrodt Institute of Radiology, and Department of Radiology, Washington University in Saint Louis, St. Louis, MO, USA., Prensky Z; LB Pharmaceuticals Inc., New York, NY, USA., Kuwabara H; Johns Hopkins University Department of Radiology, Baltimore, MD, USA., Tian L; Mallinckrodt Institute of Radiology, and Department of Radiology, Washington University in Saint Louis, St. Louis, MO, USA., Valenta I; Mallinckrodt Institute of Radiology, and Department of Radiology, Washington University in Saint Louis, St. Louis, MO, USA., Schindler TH; Mallinckrodt Institute of Radiology, and Department of Radiology, Washington University in Saint Louis, St. Louis, MO, USA., Gründer G; Central Institute of Mental Health, Department of Molecular Neuroimaging, Medical Faculty Mannheim, University of Heidelberg, Mannheim, Germany., Vaino AR; LB Pharmaceuticals Inc., New York, NY, USA. andrew@lbpharma.us.
Jazyk: angličtina
Zdroj: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology [Neuropsychopharmacology] 2024 Oct 16. Date of Electronic Publication: 2024 Oct 16.
DOI: 10.1038/s41386-024-01951-x
Abstrakt: Regulation of dopamine activity has important clinical consequences, most notably in schizophrenia. LB-102, N-methyl amisulpride, is a novel dopamine D 2/3 /5-HT 7 inhibitor being developed as a treatment for schizophrenia and other psychiatric disorders. The characteristic that is common to all current antipsychotics is their engagement of D 2 dopamine receptors. The goal of this study was to measure the dopamine receptor occupancy of orally administered LB-102 at three different doses (50, 75, and 100 mg as single doses and 50 and 100 mg as multiple doses) and at different timepoints in healthy volunteers using positron emission tomography (PET) with 11 C raclopride as a radiotracer. Results of this study (NCT04588129) showed that steady-state once daily oral dosing of 50 mg LB-102 afforded striatal dopamine occupancy (RO) in the desired 60-80% range consistently over the course of 24 h. Contrary to the often observed relationship between RO vs plasma concentrations, maximum dopamine RO significantly lagged maximum plasma concentration and showed little variability under steady state conditions. A similar phenomenon has recently been reported with a non-racemic version of amisulpride [1]. LB-102 was generally safe and well-tolerated at all doses. Results of this study were used to inform dosing in a subsequent Phase 2 clinical study in schizophrenia patients.
(© 2024. The Author(s).)
Databáze: MEDLINE
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