drugset / Trial / NCT02587715

A Study of Allogeneic Human UC-MSC and Liberation Therapy (When Associated With CCSVI) in Patients With RRMS

NCT02587715 ↗

Phase 1/2 Unknown 69 enrolled Novo Cellular Medicine Institute LLP
NaSingle-groupOpen-labelTreatment

Summary

STUDY OBJECTIVES: Primary Objective: Assessment of treatment safety based on incidence of any treatment emergent/treatment associated adverse events prior to discharge and at 1, 3, 6 and 12 months post treatment. Secondary objective: Assessment of efficacy at baseline, prior to discharge, 1 month, 3 months, 6 months and 12 months after treatment based on the following: EDSS and 29-item Multiple Sclerosis Impact Scale (MSIS-29), MS Functional Composite (MSFC) consisting of (1) Timed 25-Foot Walk, (2) 9 Hole Peg Test, and (3) Paced Auditory Serial Addition Test and gadolinium-enhanced magnetic resonance imaging (MRI)

Timeline

Start
2015-02
Primary completion
2017-02
Completion
2017-02

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Allogeneic Human Umbilical Cord Tissue-Derived Mesenchymal Stem Cells Cell therapy 50 cells Intravenous
Subject Allogeneic Human Umbilical Cord Tissue-Derived Mesenchymal Stem Cells Cell therapy 100 cells Intravenous