Page last updated: 2024-09-05

odiparcil and ARSB Deficiency

odiparcil has been researched along with ARSB Deficiency in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's3 (100.00)2.80

Authors

AuthorsStudies
Abitbol, JL; Chowdary, P; Faudot-Vernier, E; Fiquet, A; Guffon, N; Hendriksz, CJ; Hennermann, JB; Hughes, D; Huot-Marchand, P; Lacombe, O; Richard, MP; Tallandier, M; Teles, EL1
Bocart, S; Bouchot, A; Bournique, B; Broqua, P; Entchev, E; Jantzen, I; Junien, JL; Lacombe, O; Luccarini, JM; Masson, P; Tallandier, M1
Antonelli, S; Cimbolini, N; Entchev, E; Feraille, L; Germain, JM; Jantzen, I; Lacombe, O; Luccarrini, JM; Mauro, V; Roussey, A; Tallandier, M; Young, SP; Zhang, H1

Trials

1 trial(s) available for odiparcil and ARSB Deficiency

ArticleYear
Oral treatment for mucopolysaccharidosis VI: Outcomes of the first phase IIa study with odiparcil.
    Journal of inherited metabolic disease, 2022, Volume: 45, Issue:2

    Topics: Enzyme Replacement Therapy; Glycosaminoglycans; Glycosides; Humans; Mucopolysaccharidoses; Mucopolysaccharidosis VI; N-Acetylgalactosamine-4-Sulfatase

2022

Other Studies

2 other study(ies) available for odiparcil and ARSB Deficiency

ArticleYear
Odiparcil, a potential glycosaminoglycans clearance therapy in mucopolysaccharidosis VI-Evidence from in vitro and in vivo models.
    PloS one, 2020, Volume: 15, Issue:5

    Topics: Administration, Oral; Animals; Cattle; Cells, Cultured; Chondroitin Sulfates; Dermatan Sulfate; Disease Models, Animal; Endothelial Cells; Female; Glycosaminoglycans; Glycosides; Humans; In Vitro Techniques; Male; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Mucopolysaccharidosis VI; Rats; Rats, Sprague-Dawley

2020
MPS VI associated ocular phenotypes in an MPS VI murine model and the therapeutic effects of odiparcil treatment.
    Molecular genetics and metabolism, 2022, Volume: 135, Issue:2

    Topics: Animals; Disease Models, Animal; Eye; Eye Diseases; Glycosides; Humans; Mice; Mucopolysaccharidosis VI; N-Acetylgalactosamine-4-Sulfatase; Phenotype

2022