Maroteaux-Lamy Syndrome: Clinical Trials

4 trials for Maroteaux-Lamy Syndrome, newest first

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2 completed, 2 terminated. 2 Phase 2, 1 Not applicable, 1 Phase 4.

By phase and status

PhaseTrialsStatus
Phase 22Completed 1, Terminated 1
Not applicable1Terminated 1
Phase 41Completed 1

Follow Maroteaux-Lamy Syndrome: new trials by email Literature Review of Maroteaux-Lamy Syndrome trials Research Report on Maroteaux-Lamy Syndrome

Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
Naglazyme After Allo Transplant for Maroteaux-Lamy Syndrome
Naglazyme® - Maroteaux-Lamy Syndrome
Not applicableTerminatedMasonic Cancer Center, University of Minnesota12016-01-262020-12-23
Allogeneic Bone Marrow Transplant for Inherited Metabolic Disorders
Campath-1H, Cyclophosphamide, Busulfan - Mucopolysaccharidosis, Hurler Syndrome
Phase 2CompletedMasonic Cancer Center, University of Minnesota462009-12-012018-02-05
Hematopoietic Stem Cell Transplantation (HCT) for Inborn Errors of Metabolism
Stem Cell Transplantation, Cyclophosphamide, Campath-1H - Hurler's Syndrome, Maroteaux-Lamy Syndrome
Phase 2TerminatedMasonic Cancer Center, University of Minnesota182008-03-012017-12-28
A Phase 4 Two Dose Level Study of Naglazyme(TM) (Galsulfase) in Infants With MPS VI
Naglazyme - Mucopolysaccharidosis VI, Maroteaux-Lamy Syndrome
Phase 4CompletedBioMarin Pharmaceutical42006-05-012011-07-22

Narrower conditions

Mucopolysaccharidosis VI (4)  ·  Aspartylglucosaminuria (2)  ·  Fucosidosis (2)  ·  Leukodystrophy, Globoid Cell (2)  ·  Leukodystrophy, Metachromatic (2)  ·  Mucopolysaccharidosis I (2)  ·  Mucopolysaccharidosis VII (2)  ·  Peroxisomal Disorders (2)  ·  Sphingolipidoses (2)  ·  alpha-Mannosidosis (2)  ·  Adrenoleukodystrophy (1)  ·  Metabolism, Inborn Errors (1)  ·  Mucopolysaccharidoses (1)  ·  Mucopolysaccharidosis II (1)  ·  Niemann-Pick Disease, Type B (1)

Broader conditions

Carbohydrate Metabolism, Inborn Errors (4)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (4)  ·  Connective Tissue Diseases (4)  ·  Genetic Diseases, Inborn (4)  ·  Lysosomal Storage Diseases (4)  ·  Metabolic Diseases (4)  ·  Mucinoses (4)  ·  Nutritional and Metabolic Diseases (4)  ·  Skin and Connective Tissue Diseases (4)  ·  Metabolism, Inborn Errors (3)  ·  Mucopolysaccharidoses (3)  ·  Brain Diseases (2)  ·  Brain Diseases, Metabolic (2)  ·  Brain Diseases, Metabolic, Inborn (2)  ·  Central Nervous System Diseases (2)

Interventions

Alemtuzumab (2)  ·  Busulfan (2)  ·  Cyclophosphamide (2)  ·  Stem Cell Transplantation (2)  ·  galsulfase (2)  ·  Bone Marrow Transplantation (1)  ·  Cyclosporine (1)  ·  Mycophenolic Acid (1)

Sponsors

Masonic Cancer Center, University of Minnesota (3)  ·  BioMarin Pharmaceutical (1)

Countries

United States (4)  ·  France (1)  ·  Portugal (1)

Top investigators

Paul Orchard, MD (2)  ·  Celeste Decker, MD (1)  ·  Elizabeth Braulin, M.D. (1)

Results publications

PMID 21586746, PMID 24108527, PMID 33775523