drugset / Trial / NCT01199640

Study of the Safety and Efficacy of MLN1202 in Patients in Multiple Sclerosis

NCT01199640

Phase 2 Completed 50 enrolled Millennium Pharmaceuticals, Inc.
RandomizedSingle-groupSingle-blindTreatment

Summary

This was a phase 2a study of MLN1202 to determine safety, tolerability and initial efficacy in patients with relapsing-remitting multiple sclerosis (RRMS). It was conducted in 2 dose cohorts enrolling a total of 50 patients. Efficacy was assessed by comparing the numbers of new gadolinium-enhancing brain lesions during the screening and treatment periods.

Timeline

Start
2005-05
Primary completion
2007-07
Completion
2007-10

Drugs

EvaluationDrugModalityDoseRoute
Subject PLOZALIZUMAB Monoclonal antibody 4 mg/kg Intravenous
Subject PLOZALIZUMAB Monoclonal antibody 8 mg/kg Intravenous

Indications