Literature DB >> 31187454

Long-Term Neuropsychological Outcomes from an Open-Label Phase I/IIa Trial of 2-Hydroxypropyl-β-Cyclodextrins (VTS-270) in Niemann-Pick Disease, Type C1.

Cristan A Farmer1, Audrey Thurm1, Nicole Farhat2, Simona Bianconi2, Lee Ann Keener2, Forbes D Porter3.   

Abstract

BACKGROUND: Niemann-Pick disease, type C1 (NPC1) is a neurodegenerative condition that arises from mutations of NPC1 and is often diagnosed in children. Recently, several drug trials have been implemented to minimize neurodegeneration, including a trial of 2-hydroxypropyl-β-cyclodextrins (VTS-270).
OBJECTIVES: The current study extends findings from a previous report of 18 months of disease severity data by describing neuropsychological outcomes over the course of 36 months post-baseline.
DESIGN: An open-label, dose-escalation phase I/IIa study of VTS-270 was performed in participants with NPC1 aged 4-23 years.
METHODS: Fourteen participants were sequentially assigned to receive monthly initial intrathecal VTS-270 at doses of 50, 200, 300, or 400 mg per month. After initial dosing, participants were dose-escalated (to 600 or 1200 mg) as tolerated. Participants were evaluated at 6-month intervals using a standardized neuropsychological battery, including tests of cognition and adaptive behavior. A random effects model with restricted maximum likelihood estimation was constructed for each outcome, and the slope was the parameter of interest.
RESULTS: Findings based on IQ scores and both standard scores and age equivalents of adaptive functioning indicate that there were not meaningful declines in these areas during the study period. The average annualized change in Full Scale IQ was negative: B = - 1.28, standard error (SE) = 0.70, t(34.2) = - 1.83, p = 0.076. The Vineland-II Adaptive Behavior Composite standard score decreased by 1.76 points per year [SE = 0.67, t(59.1) = - 2.62, p = 0.011], but annualized slopes for each of the domain age equivalents were positive: Communication [B = 0.71, SE = 3.12, t(60.7) = 0.23, p = 0.82], Socialization [B = 2.99, SE = 2.92, t(60.4) = 1.03, p = 0.30], Daily Living Skills [B = 2.76, SE = 2.76, t(60.3) = 1.18, p = 0.24], and Motor Skills [B = 1.42, SE = 0.94, t(50.5) = 1.51, p = 0.14], indicating not worsening but slower-than-average acquisition of skills.
CONCLUSION: In conjunction with previous findings, these results provide support for the slowing of disease progress up to 36 months post-initiation of intrathecal VTS-270. REGISTRATION: ClinicalTrials.gov identifier NCT01747135: Hydroxypropyl Beta Cyclodextrin for Niemann-Pick type C1 Disease.

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Year:  2019        PMID: 31187454      PMCID: PMC7448545          DOI: 10.1007/s40263-019-00642-2

Source DB:  PubMed          Journal:  CNS Drugs        ISSN: 1172-7047            Impact factor:   5.749


  11 in total

1.  Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type C.

Authors:  Nicole M Yanjanin; Jorge I Vélez; Andrea Gropman; Kelly King; Simona E Bianconi; Sandra K Conley; Carmen C Brewer; Beth Solomon; William J Pavan; Mauricio Arcos-Burgos; Marc C Patterson; Forbes D Porter
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2010-01-05       Impact factor: 3.568

2.  Niemann-Pick C disease in Spain: clinical spectrum and development of a disability scale.

Authors:  C Iturriaga; M Pineda; E M Fernández-Valero; M T Vanier; M J Coll
Journal:  J Neurol Sci       Date:  2006-06-30       Impact factor: 3.181

3.  Cyclodextrins in the treatment of a mouse model of Niemann-Pick C disease.

Authors:  F Camargo; R P Erickson; W S Garver; G S Hossain; P N Carbone; R A Heidenreich; J Blanchard
Journal:  Life Sci       Date:  2001-11-30       Impact factor: 5.037

4.  Intracisternal cyclodextrin prevents cerebellar dysfunction and Purkinje cell death in feline Niemann-Pick type C1 disease.

Authors:  Charles H Vite; Jessica H Bagel; Gary P Swain; Maria Prociuk; Tracey U Sikora; Veronika M Stein; Patricia O'Donnell; Therese Ruane; Sarah Ward; Alexandra Crooks; Su Li; Elizabeth Mauldin; Susan Stellar; Marc De Meulder; Mark L Kao; Daniel S Ory; Cristin Davidson; Marie T Vanier; Steven U Walkley
Journal:  Sci Transl Med       Date:  2015-02-25       Impact factor: 17.956

5.  Neuropsychological profile of adult patients with Niemann-Pick C1 (NPC1) mutations.

Authors:  B Klarner; H H Klünemann; R Lürding; C Aslanidis; R Rupprecht
Journal:  J Inherit Metab Dis       Date:  2006-12-11       Impact factor: 4.982

6.  Reversal of defective lysosomal transport in NPC disease ameliorates liver dysfunction and neurodegeneration in the npc1-/- mouse.

Authors:  Benny Liu; Stephen D Turley; Dennis K Burns; Anna M Miller; Joyce J Repa; John M Dietschy
Journal:  Proc Natl Acad Sci U S A       Date:  2009-01-26       Impact factor: 11.205

7.  Genetic variations and treatments that affect the lifespan of the NPC1 mouse.

Authors:  Benny Liu; Hao Li; Joyce J Repa; Stephen D Turley; John M Dietschy
Journal:  J Lipid Res       Date:  2007-12-12       Impact factor: 5.922

8.  Cohort study of neurocognitive functioning and adaptive behaviour in children and adolescents with Niemann-Pick Disease type C1.

Authors:  Audrey Thurm; Cristan Farmer; Nicole Yanjanin Farhat; Edythe Wiggs; David Black; Forbes D Porter
Journal:  Dev Med Child Neurol       Date:  2015-11-19       Impact factor: 5.449

9.  Niemann-Pick disease type C clinical database: cognitive and coordination deficits are early disease indicators.

Authors:  Miriam Stampfer; Susanne Theiss; Yasmina Amraoui; Xuntian Jiang; Sigrid Keller; Daniel S Ory; Eugen Mengel; Christine Fischer; Heiko Runz
Journal:  Orphanet J Rare Dis       Date:  2013-02-22       Impact factor: 4.123

10.  Chronic cyclodextrin treatment of murine Niemann-Pick C disease ameliorates neuronal cholesterol and glycosphingolipid storage and disease progression.

Authors:  Cristin D Davidson; Nafeeza F Ali; Matthew C Micsenyi; Gloria Stephney; Sophie Renault; Kostantin Dobrenis; Daniel S Ory; Marie T Vanier; Steven U Walkley
Journal:  PLoS One       Date:  2009-09-11       Impact factor: 3.240

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  11 in total

1.  Correction of Niemann-Pick type C1 trafficking and activity with the histone deacetylase inhibitor valproic acid.

Authors:  Kanagaraj Subramanian; Darren M Hutt; Samantha M Scott; Vijay Gupta; Shu Mao; William E Balch
Journal:  J Biol Chem       Date:  2020-04-30       Impact factor: 5.157

Review 2.  Neuropsychological assessment in Niemann-Pick disease type C: a systematic review.

Authors:  Giuseppa Maresca; Caterina Formica; Vanessa Nocito; Desiree Latella; Simona Leonardi; Maria Cristina De Cola; Giuseppe Triglia; Placido Bramanti; Francesco Corallo
Journal:  Neurol Sci       Date:  2021-05-22       Impact factor: 3.307

3.  Concordance of the Vineland Adaptive Behavior Scales, second and third editions.

Authors:  C Farmer; D Adedipe; V H Bal; C Chlebowski; A Thurm
Journal:  J Intellect Disabil Res       Date:  2019-10-28

Review 4.  Clinical and Molecular Features of Early Infantile Niemann Pick Type C Disease.

Authors:  Berna Seker Yilmaz; Julien Baruteau; Ahad A Rahim; Paul Gissen
Journal:  Int J Mol Sci       Date:  2020-07-17       Impact factor: 5.923

Review 5.  CNS-Targeting Therapies for Lysosomal Storage Diseases: Current Advances and Challenges.

Authors:  Mariola J Edelmann; Gustavo H B Maegawa
Journal:  Front Mol Biosci       Date:  2020-11-12

Review 6.  Pluripotent Stem Cells for Disease Modeling and Drug Discovery in Niemann-Pick Type C1.

Authors:  Christin Völkner; Maik Liedtke; Andreas Hermann; Moritz J Frech
Journal:  Int J Mol Sci       Date:  2021-01-12       Impact factor: 5.923

7.  Inhibition of Histone Deacetylases 1, 2, and 3 Enhances Clearance of Cholesterol Accumulation in Niemann-Pick C1 Fibroblasts.

Authors:  Dana L Cruz; Nina Pipalia; Shu Mao; Deepti Gadi; Gang Liu; Michael Grigalunas; Matthew O'Neill; Taylor R Quinn; Andi Kipper; Andreas Ekebergh; Alexander Dimmling; Carlos Gartner; Bruce J Melancon; Florence F Wagner; Edward Holson; Paul Helquist; Olaf Wiest; Frederick R Maxfield
Journal:  ACS Pharmacol Transl Sci       Date:  2021-05-27

8.  Individualized management of genetic diversity in Niemann-Pick C1 through modulation of the Hsp70 chaperone system.

Authors:  Chao Wang; Samantha M Scott; Shuhong Sun; Pei Zhao; Darren M Hutt; Hao Shao; Jason E Gestwicki; William E Balch
Journal:  Hum Mol Genet       Date:  2020-01-01       Impact factor: 5.121

Review 9.  Cyclodextrins: Emerging Medicines of the New Millennium.

Authors:  Susana Santos Braga
Journal:  Biomolecules       Date:  2019-11-28

10.  Gender-Specific Effects of Two Treatment Strategies in a Mouse Model of Niemann-Pick Disease Type C1.

Authors:  Carsten Holzmann; Martin Witt; Arndt Rolfs; Veronica Antipova; Andreas Wree
Journal:  Int J Mol Sci       Date:  2021-03-03       Impact factor: 5.923

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