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Oral Migalastat HCl Leads to Greater Systemic Exposure and Tissue Levels of Active α-Galactosidase A in Fabry Patients when Co-Administered with Infused Agalsidase.
Warnock, David G; Bichet, Daniel G; Holida, Myrl; Goker-Alpan, Ozlem; Nicholls, Kathy; Thomas, Mark; Eyskens, Francois; Shankar, Suma; Adera, Mathews; Sitaraman, Sheela; Khanna, Richie; Flanagan, John J; Wustman, Brandon A; Barth, Jay; Barlow, Carrolee; Valenzano, Kenneth J; Lockhart, David J; Boudes, Pol; Johnson, Franklin K.
Afiliação
  • Warnock DG; University of Alabama at Birmingham School of Medicine Department of Medicine, Division of Nephrology, Birmingham, Alabama, United States of America.
  • Bichet DG; University of Montreal, Quebec, Canada.
  • Holida M; University of Iowa Children's Hospital, Iowa City, Iowa, United States of America.
  • Goker-Alpan O; LSD Research and Treatment Unit, O&O Alpan LLC, Fairfax, Virginia, United States of America.
  • Nicholls K; Department of Nephrology, Royal Melbourne Hospital, and University of Melbourne, Parkville, Victoria, Australia.
  • Thomas M; Linear Clinical Research Ltd, Queen Elizabeth II Medical Centre, and University of Western Australia, Nedlands, Western Australia.
  • Eyskens F; Universitair Ziekenhuis Antwerpen, Antwerpen, Belgium.
  • Shankar S; Emory University School of Medicine, Emory Genetics Clinic, Athens, Georgia, United States of America.
  • Adera M; Amicus Therapeutics, Cranbury, New Jersey, United States of America.
  • Sitaraman S; Amicus Therapeutics, Cranbury, New Jersey, United States of America.
  • Khanna R; Amicus Therapeutics, Cranbury, New Jersey, United States of America.
  • Flanagan JJ; Arvinas Inc, New Haven, Connecticut, United States of America.
  • Wustman BA; Institute and Clinical Center, Sunnyvale, California, United States of America.
  • Barth J; Amicus Therapeutics, Cranbury, New Jersey, United States of America.
  • Barlow C; Amicus Therapeutics, Cranbury, New Jersey, United States of America.
  • Valenzano KJ; Amicus Therapeutics, Cranbury, New Jersey, United States of America.
  • Lockhart DJ; Institute and Clinical Center, Sunnyvale, California, United States of America.
  • Boudes P; Cymabay Therapeutics, Newark, California, United States of America.
  • Johnson FK; Amicus Therapeutics, Cranbury, New Jersey, United States of America.
PLoS One ; 10(8): e0134341, 2015.
Article em En | MEDLINE | ID: mdl-26252393
UNLABELLED: Migalastat HCl (AT1001, 1-Deoxygalactonojirimycin) is an investigational pharmacological chaperone for the treatment of α-galactosidase A (α-Gal A) deficiency, which leads to Fabry disease, an X-linked, lysosomal storage disorder. The currently approved, biologics-based therapy for Fabry disease is enzyme replacement therapy (ERT) with either agalsidase alfa (Replagal) or agalsidase beta (Fabrazyme). Based on preclinical data, migalastat HCl in combination with agalsidase is expected to result in the pharmacokinetic (PK) enhancement of agalsidase in plasma by increasing the systemic exposure of active agalsidase, thereby leading to increased cellular levels in disease-relevant tissues. This Phase 2a study design consisted of an open-label, fixed-treatment sequence that evaluated the effects of single oral doses of 150 mg or 450 mg migalastat HCl on the PK and tissue levels of intravenously infused agalsidase (0.2, 0.5, or 1.0 mg/kg) in male Fabry patients. As expected, intravenous administration of agalsidase alone resulted in increased α-Gal A activity in plasma, skin, and peripheral blood mononuclear cells (PBMCs) compared to baseline. Following co-administration of migalastat HCl and agalsidase, α-Gal A activity in plasma was further significantly increased 1.2- to 5.1-fold compared to agalsidase administration alone, in 22 of 23 patients (95.6%). Importantly, similar increases in skin and PBMC α-Gal A activity were seen following co-administration of migalastat HCl and agalsidase. The effects were not related to the administered migalastat HCl dose, as the 150 mg dose of migalastat HCl increased α-Gal A activity to the same extent as the 450 mg dose. Conversely, agalsidase had no effect on the plasma PK of migalastat. No migalastat HCl-related adverse events or drug-related tolerability issues were identified. TRIAL REGISTRATION: ClinicalTrials.gov NCT01196871.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Fabry / 1-Desoxinojirimicina / Alfa-Galactosidase / Isoenzimas Tipo de estudo: Prognostic_studies Limite: Adult / Humans / Male / Middle aged Idioma: En Revista: PLoS One Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Fabry / 1-Desoxinojirimicina / Alfa-Galactosidase / Isoenzimas Tipo de estudo: Prognostic_studies Limite: Adult / Humans / Male / Middle aged Idioma: En Revista: PLoS One Ano de publicação: 2015 Tipo de documento: Article