CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 56 enrolled
Drug / intervention
MEDI-551 30 MG-IV +5 moredrug
Likely dose
MEDI-551 30 MG-IVfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01585766
NCT01585766Phase 1Completed

A Phase 1 Randomized Study of MEDI-551 in Subjects With Relapsing Forms of Multiple Sclerosis

MedImmune LLC·interventional·Posted Apr 26, 2012·Updated Oct 29, 2018

In Brief

A Phase 1 clinical trial evaluating MEDI-551 30 MG-IV, MEDI-551 60 MG-SC, and 4 other interventions for Multiple Sclerosis, Relapsing Forms. Completed, enrolled 56 participants across 16 sites in 4 countries.

Detailed Summary

The purpose of this study is to evaluate the safety and tolerability of ascending intravenous (IV) and subcutaneous (SC) doses of MEDI-551 in adult subjects with relapsing forms of multiple sclerosis (MS).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesPoland, Spain, Ukraine, United States
Collaborators--

Timeline

Phase 1CompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedApr 26, 2012
Enrollment StartApr 24, 2012
Primary CompletionJan 2, 2015
Study CompletionJun 20, 2016
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 14.2 years ago

Interventions

MEDI-551 30 MG-IVdrug

Participants received a fixed IV dose of 30 milligram (mg) MEDI-551 infused on Days 1 and 15.

MEDI-551 60 MG-SCdrug

Participants received SC injection of 60 mg MEDI-551 on Day 1.

PLACEBO-IV-SCdrug

Participants received either a fixed IV dose of placebo matching with MEDI- 551 on Days 1 and 15 or SC injection on Day 1

MEDI-551 100 MG-IVdrug

Participants received a fixed IV dose of 100 mg MEDI-551 infused on Days 1 and 15.

MEDI-551 300 MG-SCdrug

Participants received SC injection of 300 mg MEDI-551 on Day 1.

MEDI-551 600 MG-IVdrug

Participants received a fixed IV dose of 600 mg MEDI-551 infused on Days 1 and 15.