CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 54 enrolled
Drug / intervention
Intrathecal MSC-NP injection +1 morebiological
Likely dose
Not stated in 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/NCT03355365
NCT03355365Phase 2Completed

Autologous, Bone Marrow-Derived Mesenchymal Stem Cell-Derived Neural Progenitor Cells (MSC-NP), Expanded Ex Vivo; Administered Intrathecally

Tisch Multiple Sclerosis Research Center of New York·interventional·Posted Nov 28, 2017·Updated Jun 11, 2025

In Brief

A Phase 2 clinical trial evaluating Intrathecal MSC-NP injection and Intrathecal saline injection for Multiple Sclerosis. Completed, enrolled 54 participants across 1 site.

Detailed Summary

This is a phase II, double-blinded, placebo-controlled, randomized, cross-over Study designed to determine the efficacy of multiple intrathecal administrations of autologous mesenchymal stem cell-derived neural progenitor cells (MSC-NP) compared to placebo in patients with progressive multiple sclerosis. Efficacy will be measured through assessment of disability outcomes. Study participants will receive six intrathecal injections of culture-expanded autologous MSC-NPs at two month intervals in one year and six lumbar punctures as placebo treatments in a second year.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedNov 28, 2017
Enrollment StartSep 21, 2018
Primary CompletionFeb 9, 2023
Study CompletionApr 17, 2023
TodayJul 2, 2026
Enrollment to primary: 4.4 yearsPosted 8.6 years ago

Interventions

Intrathecal MSC-NP injectionbiological

MSC-NPs represent a neural subpopulation of MSCs from bone marrow with reduced pluripotency and minimized risk of ectopic differentiation, thus are likely to be more suitable for CNS delivery. Importantly, characterization of MSC-NPs demonstrated their immunoregulatory and trophic properties, and MSC-NPs derived from MS and non-MS patients alike were therapeutically viable.

Intrathecal saline injectionother

Placebo