Literature DB >> 25223731

An exploratory double-blind, randomized clinical trial with selisistat, a SirT1 inhibitor, in patients with Huntington's disease.

Sigurd D Süssmuth1, Salman Haider, G Bernhard Landwehrmeyer, Ruth Farmer, Chris Frost, Giovanna Tripepi, Claus A Andersen, Marco Di Bacco, Claudia Lamanna, Enrica Diodato, Luisa Massai, Daniela Diamanti, Elisa Mori, Letizia Magnoni, Jens Dreyhaupt, Karin Schiefele, David Craufurd, Carsten Saft, Monika Rudzinska, Danuta Ryglewicz, Michael Orth, Sebastian Brzozy, Anna Baran, Giuseppe Pollio, Ralph Andre, Sarah J Tabrizi, Borje Darpo, Goran Westerberg.   

Abstract

AIMS: Selisistat, a selective SirT1 inhibitor is being developed as a potentially disease-modifying therapeutic for Huntington's disease (HD). This was the first study of selisistat in HD patients and was primarily aimed at development of pharmacodynamic biomarkers.
METHODS: This was a randomized, double-blind, placebo-controlled, multicentre exploratory study. Fifty-five male and female patients in early stage HD were randomized to receive 10 mg or 100 mg of selisistat or placebo once daily for 14 days. Blood sampling, clinical and safety assessments were conducted throughout the study. Candidate pharmacodynamic markers included circulating soluble huntingtin and innate immune markers.
RESULTS: Selisistat was found to be safe and well tolerated, and systemic exposure parameters showed that the average steady-state plasma concentration achieved at the 10 mg dose level (125 nm) was comparable with the IC50 for SirT1 inhibition. No adverse effects on motor, cognitive or functional readouts were recorded. While circulating levels of soluble huntingtin were not affected by selisistat in this study, the biological samples collected have allowed development of assay technology for use in future studies. No effects on innate immune markers were seen.
CONCLUSIONS: Selisistat was found to be safe and well tolerated in early stage HD patients at plasma concentrations within the anticipated therapeutic concentration range.
© 2014 The British Pharmacological Society.

Entities:  

Keywords:  Huntington's disease; SirT1 inhibition; pharmacodynamics; pharmacokinetics; selisistat

Mesh:

Substances:

Year:  2015        PMID: 25223731      PMCID: PMC4345957          DOI: 10.1111/bcp.12512

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  41 in total

1.  Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data.

Authors:  Sarah J Tabrizi; Ralf Reilmann; Raymund A C Roos; Alexandra Durr; Blair Leavitt; Gail Owen; Rebecca Jones; Hans Johnson; David Craufurd; Stephen L Hicks; Christopher Kennard; Bernhard Landwehrmeyer; Julie C Stout; Beth Borowsky; Rachael I Scahill; Chris Frost; Douglas R Langbehn
Journal:  Lancet Neurol       Date:  2011-12-02       Impact factor: 44.182

2.  SIRT1 mediates central circadian control in the SCN by a mechanism that decays with aging.

Authors:  Hung-Chun Chang; Leonard Guarente
Journal:  Cell       Date:  2013-06-20       Impact factor: 41.582

Review 3.  Molecular mechanisms and potential therapeutical targets in Huntington's disease.

Authors:  Chiara Zuccato; Marta Valenza; Elena Cattaneo
Journal:  Physiol Rev       Date:  2010-07       Impact factor: 37.312

4.  Brain SIRT1: anatomical distribution and regulation by energy availability.

Authors:  Giorgio Ramadori; Charlotte E Lee; Angie L Bookout; Syann Lee; Kevin W Williams; Jason Anderson; Joel K Elmquist; Roberto Coppari
Journal:  J Neurosci       Date:  2008-10-01       Impact factor: 6.167

5.  Acetylation targets mutant huntingtin to autophagosomes for degradation.

Authors:  Hyunkyung Jeong; Florian Then; Thomas J Melia; Joseph R Mazzulli; Libin Cui; Jeffrey N Savas; Cindy Voisine; Paolo Paganetti; Naoko Tanese; Anne C Hart; Ai Yamamoto; Dimitri Krainc
Journal:  Cell       Date:  2009-04-03       Impact factor: 41.582

6.  The Pittsburgh Sleep Quality Index: a new instrument for psychiatric practice and research.

Authors:  D J Buysse; C F Reynolds; T H Monk; S R Berman; D J Kupfer
Journal:  Psychiatry Res       Date:  1989-05       Impact factor: 3.222

7.  Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY.

Authors:  Michael Orth; Olivia J Handley; Carsten Schwenke; Stephen B Dunnett; David Craufurd; Aileen K Ho; Edward Wild; Sarah J Tabrizi; G Bernhard Landwehrmeyer
Journal:  PLoS Curr       Date:  2010-09-28

8.  Opposing effects of sirtuins on neuronal survival: SIRT1-mediated neuroprotection is independent of its deacetylase activity.

Authors:  Jason A Pfister; Chi Ma; Brad E Morrison; Santosh R D'Mello
Journal:  PLoS One       Date:  2008-12-31       Impact factor: 3.240

9.  Detection of Huntington's disease decades before diagnosis: the Predict-HD study.

Authors:  J S Paulsen; D R Langbehn; J C Stout; E Aylward; C A Ross; M Nance; M Guttman; S Johnson; M MacDonald; L J Beglinger; K Duff; E Kayson; K Biglan; I Shoulson; D Oakes; M Hayden
Journal:  J Neurol Neurosurg Psychiatry       Date:  2007-12-20       Impact factor: 10.154

10.  Development of an ELISA assay for the quantification of soluble huntingtin in human blood cells.

Authors:  Luisa Massai; Lara Petricca; Letizia Magnoni; Luca Rovetini; Salman Haider; Ralph Andre; Sarah J Tabrizi; Sigurd D Süssmuth; Bernhard G Landwehrmeyer; Andrea Caricasole; Giuseppe Pollio; Simonetta Bernocco
Journal:  BMC Biochem       Date:  2013-11-25       Impact factor: 4.059

View more
  45 in total

Review 1.  [Huntington's disease].

Authors:  J D Rollnik
Journal:  Nervenarzt       Date:  2015-06       Impact factor: 1.214

Review 2.  Therapeutic approaches to Huntington disease: from the bench to the clinic.

Authors:  Nicholas S Caron; E Ray Dorsey; Michael R Hayden
Journal:  Nat Rev Drug Discov       Date:  2018-09-21       Impact factor: 84.694

Review 3.  Therapeutic Update on Huntington's Disease: Symptomatic Treatments and Emerging Disease-Modifying Therapies.

Authors:  Deepa Dash; Tiago A Mestre
Journal:  Neurotherapeutics       Date:  2020-10       Impact factor: 7.620

Review 4.  Sirtuin activators and inhibitors: Promises, achievements, and challenges.

Authors:  Han Dai; David A Sinclair; James L Ellis; Clemens Steegborn
Journal:  Pharmacol Ther       Date:  2018-03-22       Impact factor: 12.310

Review 5.  Recent Advances in the Treatment of Huntington's Disease: Targeting DNA and RNA.

Authors:  Kathleen M Shannon
Journal:  CNS Drugs       Date:  2020-03       Impact factor: 5.749

6.  Molecular Imaging of Sirtuin1 Expression-Activity in Rat Brain Using Positron-Emission Tomography-Magnetic-Resonance Imaging with [18F]-2-Fluorobenzoylaminohexanoicanilide.

Authors:  Robin Bonomi; Vadim Popov; Maxwell T Laws; David Gelovani; Anjoy Majhi; Aleksandr Shavrin; Xin Lu; Otto Muzik; Nashaat Turkman; Renshyan Liu; Thomas Mangner; Juri G Gelovani
Journal:  J Med Chem       Date:  2018-08-13       Impact factor: 7.446

Review 7.  Huntington's Disease-Update on Treatments.

Authors:  Kara J Wyant; Andrew J Ridder; Praveen Dayalu
Journal:  Curr Neurol Neurosci Rep       Date:  2017-04       Impact factor: 5.081

Review 8.  PGC-1α, Sirtuins and PARPs in Huntington's Disease and Other Neurodegenerative Conditions: NAD+ to Rule Them All.

Authors:  Alejandro Lloret; M Flint Beal
Journal:  Neurochem Res       Date:  2019-05-07       Impact factor: 3.996

9.  Dual and Opposing Roles of MicroRNA-124 in Epilepsy Are Mediated through Inflammatory and NRSF-Dependent Gene Networks.

Authors:  Gary P Brennan; Deblina Dey; Yuncai Chen; Katelin P Patterson; Eric J Magnetta; Alicia M Hall; Celine M Dube; Yu-Tang Mei; Tallie Z Baram
Journal:  Cell Rep       Date:  2016-03-03       Impact factor: 9.423

Review 10.  Histone Deacetylases Take Center Stage on Regulation of Podocyte Function.

Authors:  Min Liu; Zhe Qiao; Yang Zhang; Ping Zhan; Fan Yi
Journal:  Kidney Dis (Basel)       Date:  2020-04-29
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.