drugset / Trial / NCT00548769
Firategrast (SB683699) Surface Area Study in Multiple Sclerosis Patients
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Firategrast | Small molecule | 900 mg | Oral |