drugset / Trial / NCT00548769

Firategrast (SB683699) Surface Area Study in Multiple Sclerosis Patients

NCT00548769 ↗

Phase 1 Completed 37 enrolled GlaxoSmithKline
RandomizedCrossoverOpen-labelTreatment

Summary

Sufficient subjects with a confirmed diagnosis of MS (EDSS score of 6.5 or below), will be recruited to ensure that 30 subjects (approx. equal numbers of each gender) complete the study. Subjects will undergo a screening visit, then four study days, each separated by a washout period of at least 7 days, when the different firategrast batches of drug substance will be administered, and a follow-up visit.

Timeline

Start
2007-04-21
Primary completion
2007-11-26
Completion
2007-11-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Firategrast Small molecule 900 mg Oral

Indications