New stem cell approach aims to tame rare genetic diseases
NCT ID NCT02171104
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a stem cell transplant method for people with inherited metabolic disorders and severe osteopetrosis. The goal is to get the donor cells to take hold while keeping side effects low. Participants receive chemotherapy drugs before the transplant to prepare their bodies. The trial includes 149 people aged 0 to 55.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- stem cell transplant with chemotherapy drugs (busulfan, fludarabine, and sometimes ATG or other agents)
- What this could lead to
- If successful, this could offer a way to slow or stop the progression of severe inherited metabolic disorders and osteopetrosis, potentially improving quality of life and survival.
- What could go wrong
- This is a phase 2 trial with 149 participants, so results are still early. The transplant procedure carries serious risks, including graft failure, severe infections, and organ damage.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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149 people
The number who actually took part.
- Started
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Jul 2014
- Expected to finish
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Jul 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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Up to 55 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 0 through 55 years of age * Adequate graft available * Adequate organ function * Eligible Diseases: * Mucopolysaccharidosis Disorders: * MPS IH (Hurler syndrome) * MPS II (Hunter syndrome) if the patient has no or minimal evidence of symptomatic neurologic disease but is expected to have a neurologic phenotype * MPS VI (Maroteaux-Lamy syndrome) * MPS VII (Sly syndrome) * Glycoprotein Metabolic Disorders: * Alpha mannosidosis * Fucosidosis * Aspartylglucosaminuria * Sphingolipidoses and Recessive Leukodystrophies: * Globoid cell leukodystrophy * Metachromatic leukodystrophy * Niemann-Pick B patients (sphingomyelin deficiency) * Niemann-Pick C subtype 2 * Peroxisomal Disorders: * Adrenoleukodystrophy with cerebral involvement * Zellweger syndrome * Neonatal Adrenoleukodystrophy * Infantile Refsum disease * Acyl-CoA-Oxidase Deficiency * D-Bifunctional enzyme deficiency * Multifunctional enzyme deficiency * Alpha-methylacyl-CoA Racmase Deficiency (AMACRD) * Mitochondrial Neurogastrointestingal Encephalopathy (MNGIE) * Severe Osteopetrosis (OP) * Hereditary Leukoencephalopathy with axonal spheroids (HDLS; CSF1R mutation) * Other Inherited Metabolic Disorders (IMD): Patients will also be considered who have other life-threatening, rare lysosomal, peroxisomal or other similar inherited disorders characterized by white matter disease or other neurologic manifestations for which there is rationale that transplantation would be of benefit, such as certain patients with Wolman's disease, GM1 gangliosidosis, I-cell disease, Tay-Sachs disease, Sandhoff disease or others. * Voluntary written consent Exclusion Criteria: * Pregnancy - menstruating females must have a negative serum or urine pregnancy test within 14 days of study treatment start * Prior myeloablative chemotherapy exposure within 4 months of the start of conditioning on this protocol (patients excluded for this reason may be eligible for other institutional protocols) * Uncontrolled bacterial, fungal or viral infections including HIV (including active infection with Aspergillus or other mold within 30 days)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Masonic Cancer Center, University of Minnesota
Minneapolis, Minnesota, 55455, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Half-Matched stem cell transplant offers hope for children with rare immune and metabolic diseases
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- Early enzyme therapy may help kids with rare disease grow better