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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

Project: Research

Project Details

StatusFinished
Effective start/end date02/1/1006/1/23

Funding

  • Actelion Clinical Research Incorporated: $108,448.75