Fosmetpantotenate Randomized Controlled Trial in Pantothenate Kinase-Associated Neurodegeneration.


Journal

Movement disorders : official journal of the Movement Disorder Society
ISSN: 1531-8257
Titre abrégé: Mov Disord
Pays: United States
ID NLM: 8610688

Informations de publication

Date de publication:
06 2021
Historique:
revised: 20 10 2020
received: 18 07 2020
accepted: 26 10 2020
pubmed: 18 11 2020
medline: 24 6 2021
entrez: 17 11 2020
Statut: ppublish

Résumé

Pantothenate kinase-associated neurodegeneration (PKAN) currently has no approved treatments. The Fosmetpantotenate Replacement Therapy pivotal trial examined whether treatment with fosmetpantotenate improves PKAN symptoms and stabilizes disease progression. This randomized, double-blind, placebo-controlled, multicenter study evaluated fosmetpantotenate, 300 mg oral dose three times daily, versus placebo over a 24-week double-blind period. Patients with pathogenic variants of PANK2, aged 6 to 65 years, with a score ≥6 on the PKAN-Activities of Daily Living (PKAN-ADL) scale were enrolled. Patients were randomized to active (fosmetpantotenate) or placebo treatment, stratified by weight and age. The primary efficacy endpoint was change from baseline at week 24 in PKAN-ADL. Between July 23, 2017, and December 18, 2018, 84 patients were randomized (fosmetpantotenate: n = 41; placebo: n = 43); all 84 patients were included in the analyses. Six patients in the placebo group discontinued treatment; two had worsening dystonia, two had poor compliance, and two died of PKAN-related complications (aspiration during feeding and disease progression with respiratory failure, respectively). Fosmetpantotenate and placebo group PKAN-ADL mean (standard deviation) scores were 28.2 (11.4) and 27.4 (11.5) at baseline, respectively, and were 26.9 (12.5) and 24.5 (11.8) at week 24, respectively. The difference in least square mean (95% confidence interval) at week 24 between fosmetpantotenate and placebo was -0.09 (-1.69 to 1.51; P = 0.9115). The overall incidence of treatment-emergent serious adverse events was similar in the fosmetpantotenate (8/41; 19.5%) and placebo (6/43; 14.0%) groups. Treatment with fosmetpantotenate was safe but did not improve function assessed by the PKAN-ADL in patients with PKAN. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Sections du résumé

BACKGROUND
Pantothenate kinase-associated neurodegeneration (PKAN) currently has no approved treatments.
OBJECTIVES
The Fosmetpantotenate Replacement Therapy pivotal trial examined whether treatment with fosmetpantotenate improves PKAN symptoms and stabilizes disease progression.
METHODS
This randomized, double-blind, placebo-controlled, multicenter study evaluated fosmetpantotenate, 300 mg oral dose three times daily, versus placebo over a 24-week double-blind period. Patients with pathogenic variants of PANK2, aged 6 to 65 years, with a score ≥6 on the PKAN-Activities of Daily Living (PKAN-ADL) scale were enrolled. Patients were randomized to active (fosmetpantotenate) or placebo treatment, stratified by weight and age. The primary efficacy endpoint was change from baseline at week 24 in PKAN-ADL.
RESULTS
Between July 23, 2017, and December 18, 2018, 84 patients were randomized (fosmetpantotenate: n = 41; placebo: n = 43); all 84 patients were included in the analyses. Six patients in the placebo group discontinued treatment; two had worsening dystonia, two had poor compliance, and two died of PKAN-related complications (aspiration during feeding and disease progression with respiratory failure, respectively). Fosmetpantotenate and placebo group PKAN-ADL mean (standard deviation) scores were 28.2 (11.4) and 27.4 (11.5) at baseline, respectively, and were 26.9 (12.5) and 24.5 (11.8) at week 24, respectively. The difference in least square mean (95% confidence interval) at week 24 between fosmetpantotenate and placebo was -0.09 (-1.69 to 1.51; P = 0.9115). The overall incidence of treatment-emergent serious adverse events was similar in the fosmetpantotenate (8/41; 19.5%) and placebo (6/43; 14.0%) groups.
CONCLUSIONS
Treatment with fosmetpantotenate was safe but did not improve function assessed by the PKAN-ADL in patients with PKAN. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Identifiants

pubmed: 33200489
doi: 10.1002/mds.28392
pmc: PMC8246547
doi:

Substances chimiques

Pantothenic Acid 19F5HK2737
fosmetpantotenate VA101M0K2F

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1342-1352

Informations de copyright

© 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

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Auteurs

Thomas Klopstock (T)

Friedrich Baur Institute at the Department of Neurology, University Hospital, LMU Munich, Munich, Germany.
German Center for Neurodegenerative Diseases (DZNE), Munich, Munich, Germany.
Munich Cluster for Systems Neurology (SyNergy), Munich, Munich, Germany.

Aleksandar Videnovic (A)

Department of Neurology, Massachusetts General Hospital/Harvard Medical School, Boston, Massachusetts, USA.

Almut Turid Bischoff (AT)

Friedrich Baur Institute at the Department of Neurology, University Hospital, LMU Munich, Munich, Germany.

Cecilia Bonnet (C)

Department of Neurology, Sorbonne University, AP-HP Salpêtrière Hospital, Paris, France.

Laura Cif (L)

Department of Neurosurgery, CHRU de Montpellier, Gui de Chauliac Hospital, Montpellier, France.

Cynthia Comella (C)

Department of Neurosurgery and Neurological Sciences, Rush University Medical Center, Chicago, Illinois, USA.

Marta Correa-Vela (M)

Department of Child Neurology, Hospital Universitari Vall d'Hebron, Barcelona, Spain.

Maria L Escolar (ML)

Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Jamie L Fraser (JL)

Rare Disease Institute, Division of Genetics and Metabolism, Children's National Medical Center, Washington, District of Columbia, USA.

Victoria Gonzalez (V)

Department of Neurosurgery, University Hospital of Montpellier, Gui de Chauliac Hospital, Montpellier, France.

Neal Hermanowicz (N)

Department of Neurology, University of California Irvine, Irvine, California, USA.

Robert Jech (R)

Department of Neurology, First Faculty of Medicine, Charles University and General Faculty Hospital, Prague, Czech Republic.

Hyder A Jinnah (HA)

Departments of Neurology and Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA.

Tomasz Kmiec (T)

Child Neurology Department, Children's Memorial Health Institute, Warsaw, Poland.

Anthony Lang (A)

Edmond J. Safra Program in Parkinson's Disease and the Department of Medicine (Neurology), Toronto Western Hospital and the University of Toronto, Toronto, Ontario, Canada.

Maria J Martí (MJ)

Movement Disorders Unit, Hospital Clinic of Barcelona, European Reference Network for Rare Neurological Diseases (ERN-RND), Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED. CB06/05/0018-ISCIII), Barcelona, Spain.

Saadet Mercimek-Andrews (S)

Division of Clinical and Metabolic Genetics, Department of Pediatrics, University of Toronto, The Hospital for Sick Children, Toronto, Ontario, Canada.

Migvis Monduy (M)

Neurology, Nicklaus Children's Hospital, Miami, Florida, USA.

Graeme A M Nimmo (GAM)

Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

Belen Perez-Dueñas (B)

Department of Child Neurology, Hospital Universitari Vall d'Hebron, Barcelona, Spain.

Helle Cecilie Viekilde Pfeiffer (HCV)

Department of Child Neurology, Oslo University Hospital-Rikshospitalet, Oslo, Norway.

Lluis Planellas (L)

Department of Neurology, Hospital Clinic of Barcelona, Barcelona, Spain.

Emmanuel Roze (E)

Department of Neurology, Sorbonne University, AP-HP Salpêtrière Hospital, Brain and Spine Institute, Paris, France.

Nivedita Thakur (N)

Department of Pediatrics, Division of Child and Adolescent Neurology, University of Texas at Houston Medical School, Houston, Texas, USA.

Laura Tochen (L)

Department of Neurology, Children's National Medical Center, Washington, District of Columbia, USA.

Nora Vanegas-Arroyave (N)

Department of Neurology, Columbia University College of Physicians and Surgeons, New York, New York, USA.

Giovanna Zorzi (G)

Department of Child Neurology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.

Colleen Burns (C)

Biostatistics, Retrophin, Inc., San Diego, California, USA.

Feriandas Greblikas (F)

Research and Development, Retrophin, Inc., San Diego, California, USA.

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