drugset / Trial / NCT02048358

Safety, Pharmacokinetics and Pharmacodynamics Study With 2B3-201 in Healthy Subjects and Multiple Sclerosis(MS) Patients

NCT02048358 ↗

Phase 1 Terminated 47 enrolled BBB-Therapeutics B.V.

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

EvaluationDrugModalityDoseRoute
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

Indications