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Clinical Trial Summary

The purpose of this study is to determine the maximum tolerated dose (MTD) of mesenchymal stem cells (IT-MSC) in patients with active, advanced cerebral adrenoleukodystrophy (cALD).


Clinical Trial Description

This is a single-institution dose escalation study to determine the maximum tolerated dose (MTD) of intrathecally administered allogeneic, 3rd party mesenchymal stem cells (IT-MSC) in patients with active, advanced cerebral adrenoleukodystrophy (cALD). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02410239
Study type Interventional
Source Masonic Cancer Center, University of Minnesota
Contact
Status Withdrawn
Phase Phase 1
Start date June 2015
Completion date July 2022

See also
  Status Clinical Trial Phase
Active, not recruiting NCT04528706 - A Clinical Study in Male Pediatric Patients With Cerebral X-linked Adrenoleukodystrophy (Cald) to Assess the Effects of MIN-102 Treatment on Disease Progression Prior to Human Stem Cell Transplant (HSCT) Phase 2
Recruiting NCT03789721 - Adrenoleukodystrophy National Registry Study
Terminated NCT03367546 - Haploidentical Allogeneic Hematopoietic Stem Cell Transplantation (HaploHCT) Following Reduced Intensity Conditioning (RIC) for Selected High Risk Non-Malignant Diseases Phase 2
Recruiting NCT06030648 - MT2022-01: MSCs for ALD Phase 1