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A phase 2 trial of the GSK-3 inhibitor tideglusib in progressive supranuclear palsy
Movement disorders, 2014-04, Vol.29 (4), p.470-478
Tolosa, Eduardo
Litvan, Irene
Höglinger, Günter U.
Burn, David
Lees, Andrew
Andrés, María V.
Gómez-Carrillo, Belén
León, Teresa
del Ser, Teodoro
2014
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Tolosa, Eduardo
Litvan, Irene
Höglinger, Günter U.
Burn, David
Lees, Andrew
Andrés, María V.
Gómez-Carrillo, Belén
León, Teresa
del Ser, Teodoro
Titel
A phase 2 trial of the GSK-3 inhibitor tideglusib in progressive supranuclear palsy
Ist Teil von
Movement disorders, 2014-04, Vol.29 (4), p.470-478
Ort / Verlag
United States: Blackwell Publishing Ltd
Erscheinungsjahr
2014
Quelle
Wiley Online Library Journals Frontfile Complete
Beschreibungen/Notizen
ABSTRACT It is believed that glycogen synthase kinase‐3 (GSK‐3) hyperphosphorylates tau protein in progressive supranuclear palsy (PSP). The Tau Restoration on PSP (TAUROS) study was a double‐blind, placebo‐controlled, randomized trial to assess the efficacy, safety, and tolerability of tideglusib, a GSK‐3 inhibitor, as potential treatment for PSP. The study enrolled 146 PSP patients with mild‐to‐moderate disease who were randomized to receive once‐daily 600 mg tideglusib, 800 mg tideglusib, or placebo (ratio, 2:2:1) administered orally over 52 weeks. The primary endpoint was the change from baseline to week 52 on the PSP rating scale. Secondary endpoints were safety and tolerability of tideglusib, changes in motor function (the Timed Up and Go Test), cognition (Dementia Rating Scale‐2, Frontal Assessment Battery, verbal fluency), apathy (Starkstein scale), activities of daily living (Schwab and England scale; Unified Parkinson's Disease Rating Scale, part II), quality of life (EuroQol), and Global Clinical Assessment. Brain atrophy on magnetic resonance imaging and several biomarkers in plasma and cerebrospinal fluid also were examined. No significant differences were detected in the primary or secondary endpoints at week 52 between placebo and either dose of tideglusib. Tideglusib was safe, with the exception of some asymptomatic, transient, and reversible transaminase elevations (mainly alanine aminotransferase) in 9% of patients, and diarrhea in 13% of patients. Tideglusib was generally well tolerated but it did not show clinical efficacy in patients with mild‐to‐moderate PSP. © 2014 International Parkinson and Movement Disorder Society
Sprache
Englisch
Identifikatoren
ISSN: 0885-3185
eISSN: 1531-8257
DOI: 10.1002/mds.25824
Titel-ID: cdi_proquest_miscellaneous_1627984566
Format
–
Schlagworte
Activities of Daily Living
,
Aged
,
Cognition - drug effects
,
Double-Blind Method
,
Enzyme Inhibitors - adverse effects
,
Enzyme Inhibitors - pharmacology
,
Enzyme Inhibitors - therapeutic use
,
Female
,
Glycogen Synthase Kinase 3 - antagonists & inhibitors
,
GSK-3
,
Humans
,
Male
,
Middle Aged
,
Motor Activity - drug effects
,
Movement disorders
,
pharmacological treatment
,
progressive supranuclear palsy
,
randomized controlled clinical trial
,
Supranuclear Palsy, Progressive - drug therapy
,
Thiadiazoles - adverse effects
,
Thiadiazoles - pharmacology
,
Thiadiazoles - therapeutic use
,
tideglusib
,
Treatment Outcome
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