Pharmacological effects of CS-0777, a selective sphingosine 1-phosphate receptor-1 modulator: Results from a 12-week, open-label pilot study in multiple sclerosis patients

被引:28
作者
Moberly, James B. [1 ]
Ford, Daniel M. [1 ]
Zahir, Hamim [1 ]
Chen, Shuquan [1 ]
Mochizuki, Takashi [1 ]
Truitt, Kenneth E. [1 ]
Vollmer, Timothy L. [2 ]
机构
[1] Daiichi Sankyo Pharma Dev, Edison, NJ 08837 USA
[2] Univ Colorado, Hlth Sci Ctr, Dept Neurol, Sch Med,Acad Off, Aurora, CO 80045 USA
关键词
S1PR1; Lymphopenia; CD8 T cell subsets; Bradycardia; Fingolimod; Autoimmune disease; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; ORAL FINGOLIMOD; LYMPHOCYTE EGRESS; HEALTHY-SUBJECTS; HEART-RATE; FTY720; EFFICACY; AGONISTS; S1P(1); RATS;
D O I
10.1016/j.jneuroim.2012.03.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CS-0777 is a selective sphingosine 1-phosphate receptor-1 modulator under investigation for treatment of multiple sclerosis (MS). We conducted an open-label, pilot study in 25 MS patients to assess the safety, pharmacokinetics, pharmacodynamics and exploratory efficacy of oral CS-0777 (0.1, 0.3 and 0.6 mg), administered once weekly or every other week for 12 weeks. CS-0777 resulted in a pronounced, dose-dependent decrease in lymphocytes and CD4 T cell subsets, which returned to baseline within 4 weeks after the last dose. Overall, CS-0777 was safe and well-tolerated. These results require confirmation in a double-blind, placebo-controlled and adequately powered phase 2 study in MS. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:100 / 107
页数:8
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