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Enrolling By Invitation NCT05634512

Evaluation of Intravenous Laronidase Pharmacokinetics Before and After Hematopoietic Cell Transplantation in Patients With Mucopolysaccharidosis Type IH.

Conditions: Hematopoietic Cell Transplantation, Mucopolysaccharidosis Type I

Sex: All
Ages: 0 Years – 3 Years
Enrollment: 24
Sponsor: Masonic Cancer Center, University of Minnesota

Location: United States

Summary

This is a prospective, observational multicenter study to collect blood from patients with mucopolysaccharidosis type IH undergoing laronidase therapy and a stem cell transplant.Sixteen patients will be enrolled over a 24 month period.

Eligibility Criteria

Inclusion Criteria:Between 0 to 3 years of ageMeet protocol specific eligibility criteria for allogeneic HCT for MPS IHPlanning to receive laronidase both pre and post-transplant in an inpatient setting as part of standard-of-care treatment. Virtually all patients with MPSIH being considered for transplantation at the University of Minnesota are already receiving enzyme infusions, and it is standard practice to continue to give enzyme infusions to 8 weeks post-transplant. Therefore, participation will not modify the treatment course.Exclusion Criteria:Patient's parent/ legal guardians are unable to provide informed consent.

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05634512). StuddyBuddy aggregates publicly available trial information.