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Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Dose-Finding Study to Evaluate the Efficacy, Safety, and Tolerability of Three Doses of ACT-128800, an Oral S1P1 Receptor Agonist, Administered for Twenty-Four Weeks
Coyle, Patricia K
(PI)
Krupp, Lauren
(CoPI)
Melville, Patricia
(CoPI)
Stony Brook University
Project
:
Research
Overview
Project Details
Status
Finished
Effective start/end date
02/1/10
→
06/1/23
Funding
Actelion Clinical Research Incorporated:
$108,448.75
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