MT2014-14 IT-MSC for Advanced Cerebral Adrenoleukodystrophy (cALD)
Stopped: Research cancelled
0Started 2015-06
Plain-language 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).
Who can participate
Age range4 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Age ≥ 4 years at time of study enrollment
* Diagnosis of ALD - the diagnosis of ALD can be made by either biochemical or molecular/genetic evidence (plasma VLCFA or ABCD1 mutation analysis) supportive of ALD as the cause of cerebral demyelination
* Evidence of active cerebral disease - defined as the presence of gadolinium enhancement on a single brain MRI study - MRI used for eligibility determination may be performed at an outside institution; the most recent MRI used to determine eligibility must be within 2 calendar months of the date of enrollment on this study
* ALD MRI (Loes) score ≥ 10
* Off of N-acetylcysteine, systemic immunosuppressive drugs or any other therapeutic intervention (except hydrocortisone and/or fludracortisone for the treatment of adrenal insufficiency) for ≥ 10 days prior to the first IT-MSC dose
* Life expectancy of \>6 months as determined by the enrolling researcher and documented in the medical record
* Voluntary written consent provided by parent(s)/guardian(s)
Exclusion Criteria:
* A candidate for allogeneic hematopoietic stem cell transplantation as determined by the University of Minnesota Inherited Metabolic and Storage Disease group
* Inability to undergo sedation, lumbar puncture or MRI studies for any reason
* Inability to stay in Minnesota for therapy through the day 28 evaluation
What they're measuring
1
Maximum Tolerated Dose
Timeframe: Day 28 post intrathecal injection of MSC
Trial details
NCT IDNCT02410239
SponsorMasonic Cancer Center, University of Minnesota