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Clinical Trials/NCT06030648
NCT06030648
Suspended
Phase 1

Intravenous Administration of Mesenchymal Stem Cells (IV-MSC) for the Treatment of Cerebral Adrenoleukodystrophy (cALD)

Masonic Cancer Center, University of Minnesota1 site in 1 country10 target enrollmentAugust 28, 2023

Overview

Phase
Phase 1
Intervention
Mesenchymal stem cells (IV-MSC)
Conditions
Cerebral Adrenoleukodystrophy
Sponsor
Masonic Cancer Center, University of Minnesota
Enrollment
10
Locations
1
Primary Endpoint
Safety and tolerability of intravenously-administered allogeneic, third-party mesenchymal stem cells (IV-MSC).
Status
Suspended
Last Updated
11 months ago

Overview

Brief Summary

This is a single-institution study to evaluate the use of intravenously administered allogeneic, 3rd party mesenchymal stem cells (IV-MSC) in patients with active, cerebral adrenoleukodystrophy (CALD), as a bridge to hematopoietic stem cell transplant or gene therapy, or in patients who are too advanced for gene therapy or HSCT. The intervention will occur in the time between diagnosis of active CALD and transplant which is currently 8-12 weeks.

Registry
clinicaltrials.gov
Start Date
August 28, 2023
End Date
May 1, 2028
Last Updated
11 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • age ≥ 3 years
  • diagnosis of ALD, as established by elevation of very long chain fatty acid levels or gene mutation
  • evidence of active cerebral disease as determined by the presence of gadolinium enhancement
  • ALD MRI (Loes) score ≥ 1
  • Patients who have not received prior gene therapy or transplant
  • Life expectancy of \> 6 months as determined by the enrolling researcher
  • Have adequate organ function confirmed by laboratory values obtained within 28 days prior to enrollment

Exclusion Criteria

  • Inability to undergo sedation or MRI studies for any reason
  • Other concurrent life-threatening disease (life expectancy \<6 months) or eligible for hospice care
  • Known or suspected hypersensitivity to human serum albumin, diphenhydramine, acetaminophen, methylprednisolone, or any of the components of IMS001.

Arms & Interventions

IV-MSC for cALD (Early Disease/Bridge Therapy)

Patients with active, cerebral adrenoleukodystrophy (cALD) as a bridge to hematopoietic stem cell transplant or gene therapy.

Intervention: Mesenchymal stem cells (IV-MSC)

IV-MSC for cALD (Advanced Disease)

Patients with active, cerebral adrenoleukodystrophy (cALD) who are too advanced for gene therapy or HSCT.

Intervention: Mesenchymal stem cells (IV-MSC)

Outcomes

Primary Outcomes

Safety and tolerability of intravenously-administered allogeneic, third-party mesenchymal stem cells (IV-MSC).

Time Frame: 6 months

Safety and tolerability of cerebral adrenoleukodystrophy (cALD) patients receiving intravenously-administered allogeneic, third-party mesenchymal stem cells (IV-MSC) assessed by incidence of adverse events.

Secondary Outcomes

  • Incidence of radiographic response in patients receiving intravenously-administered allogeneic, third-party mesenchymal stem cells (IV-MSC).(6 months)

Study Sites (1)

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