drugset / Trial / NCT00616733

12-week Safety Evaluation of Oral CS-0777 in Multiple Sclerosis Patients

NCT00616733 ↗

Phase 1 Completed 25 enrolled Daiichi Sankyo
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a 12-week study to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of oral CS-0777 in patients with Multiple Sclerosis.

Timeline

Start
2008-03
Primary completion
2010-09
Completion
2010-09

Drugs

EvaluationDrugModalityDoseRoute
Subject CS-0777 Unknown 0.1 mg Oral
Subject CS-0777 Unknown 0.3 mg Oral
Subject CS-0777 Unknown 0.6 mg Oral

Indications