drugset / Trial / NCT02048358
Safety, Pharmacokinetics and Pharmacodynamics Study With 2B3-201 in Healthy Subjects and Multiple Sclerosis(MS) Patients
Summary
In this first in human study the aim is to assess the safety, pharmacokinetics and pharmacodynamics of 2B3-201 in a randomized, first in human, double-blind, placebo- and active comparator- controlled 3-way crossover study in 18 healthy male subjects (part 1). Furthermore, the findings obtained from part 1 will be extended and confirmed in a subsequent parallel open label study in 18 healthy male and 12 MS patients and an open label study with methylprednisolone as comparator in 12 female volunteers (part 2).
Timeline
- Start
- 2013-11
- Primary completion
- 2015-01
- Completion
- 2015-02
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | 2B3-201 | Unknown | 150 mg | Intravenous |
| Subject | 2B3-201 | Unknown | 300 mg | Intravenous |
| Subject | 2B3-201 | Unknown | 450 mg | Intravenous |
| Subject | Methylprednisolone hemisuccinate | Unknown | 300 mg | Intravenous |
| Subject | Methylprednisolone hemisuccinate | Unknown | 1000 mg | Intravenous |