Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Yu‐Luan Chen"'
Publikováno v:
Pharmacology Research & Perspectives, Vol 12, Iss 2, Pp n/a-n/a (2024)
Abstract Ulotaront (SEP‐363856) is a TAAR1 agonist, with 5‐HT1A agonist activity, currently in clinical development for the treatment of schizophrenia. In vitro studies indicate ulotaront is an OCT2‐specific inhibitor with IC50 of 1.27 μM. The
Externí odkaz:
https://doaj.org/article/6ab6e839dc2b4529b1b2f4f221971a6c
Autor:
Yu-Luan Chen, Hironobu Tsukada, Snezana Milanovic, Lei Shi, Yan Li, Yongcai Mao, Kenneth S. Koblan, Gerald R. Galluppi
Publikováno v:
Neurology and Therapy, Vol 12, Iss 3, Pp 815-832 (2023)
Abstract Introduction Ulotaront (SEP-363856), a dual trace animeassociated receptor 1 (TAAR1) and 5-HT1A receptor agonist, is in phase 3 clinical development for the treatment of schizophrenia. This study evaluated the comparative bioequivalence (BE)
Externí odkaz:
https://doaj.org/article/e6aa69b4bb0544e5afb9f1d477d9b8a5
Autor:
Siqing Fu, David E. Piccioni, Hongtao Liu, Rimas V. Lukas, Santosh Kesari, Dawit Aregawi, David S. Hong, Kenichiro Yamaguchi, Kate Whicher, Yi Zhang, Yu-Luan Chen, Nagaraju Poola, John Eddy, David Blum
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract WT2725 is a Wilms’ tumor gene 1 (WT1)-derived-oligopeptide vaccine designed to induce WT1-specific cytotoxic T-lymphocytes against WT1+ tumors in human leukocyte antigen (HLA)-A*0201+ and/or HLA-A*0206+ patients. Here, we report the result
Externí odkaz:
https://doaj.org/article/60746137df784b578782dc3342f39baf
Autor:
Guangqing Xiao, Yu-Luan Chen, Nina Dedic, Linghong Xie, Kenneth S. Koblan, Gerald R. Galluppi
Publikováno v:
Pharmaceutical Research. 39:837-850
Purpose Ulotaront (SEP-363856) is a TAAR1 agonist with 5-HT1A agonist activity currently in clinical development for the treatment of schizophrenia. The objectives of the current study were to characterize the in vitro ADME properties, preclinical PK
Publikováno v:
Drug Metabolism and Bioanalysis Letters. 15:38-50
Objective: The study aims to explore the human in vivo metabolism of SEP-227900 (4H-furo[3, 2-b] pyrrole-carboxylic acid, m.w 151.03), a D-amino-acid oxidase (DAAO) inhibitor, by using plasma and urine samples from first-in-human study. Methods: The
Publikováno v:
Bioanalysis. 13:959-968
Aim: Glycopyrrolate (GLY) has been widely used to treat chronic obstructive pulmonary disease (COPD). Recent technical advancement significantly improves the drug delivery efficiency. In a clinical dose-range determination study via electronic nebuli
Autor:
Lei Shi, Zhong-Ping John Lin, Soujanya Sunkaraneni, Yu-Luan Chen, John Eddy, Armand Gatien Ngounou Wetie, Weimin Wang
Publikováno v:
The Journal of Applied Laboratory Medicine. 5:41-53
BackgroundThe development of more efficient drug delivery devices for ciclesonide inhalation products requires an ultrasensitive bioanalytical method to measure systematic exposure of ciclesonide (CIC) and its active metabolite desisobutyryl-cicleson
Autor:
Kate Whicher, Santosh Kesari, Hongtao Liu, Rimas V. Lukas, David S. Hong, Dawit Aregawi, Siqing Fu, David Piccioni, David Blum, Kenichiro Yamaguchi, Yi Zhang, John Eddy, Yu-Luan Chen, Nagaraju Poola
Publikováno v:
Scientific Reports
Scientific reports, vol 11, iss 1
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Scientific reports, vol 11, iss 1
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
WT2725 is a Wilms’ tumor gene 1 (WT1)-derived-oligopeptide vaccine designed to induce WT1-specific cytotoxic T-lymphocytes against WT1+ tumors in human leukocyte antigen (HLA)-A*0201+ and/or HLA-A*0206+ patients. Here, we report the results of a ph
Publikováno v:
Drug metabolism and bioanalysis letters. 15(1)
The study aims to explore the human in vivo metabolism of SEP-227900 (4H-furo[3, 2-b] pyrrole-carboxylic acid, m.w 151.03), a D-amino-acid oxidase (DAAO) inhibitor, by using plasma and urine samples from first-in-human study.The human plasma and urin
Publikováno v:
Journal of Applied Bioanalysis, Vol 5, Iss 2, Pp 20-33 (2019)
OBJECTIVES: Develop and validate a simple and rapid LC-MS/MS method for plasma D-serine measurement to support clinical development of a potential D-amino-acid oxidase (DAAO) inhibitor. METHODS: Calibration standards in phosphate buffered saline (PBS