Literature DB >> 24873720

Davunetide in patients with progressive supranuclear palsy: a randomised, double-blind, placebo-controlled phase 2/3 trial.

Adam L Boxer1, Anthony E Lang2, Murray Grossman3, David S Knopman4, Bruce L Miller5, Lon S Schneider6, Rachelle S Doody7, Andrew Lees8, Lawrence I Golbe9, David R Williams10, Jean-Cristophe Corvol11, Albert Ludolph12, David Burn13, Stefan Lorenzl14, Irene Litvan15, Erik D Roberson16, Günter U Höglinger17, Mary Koestler5, Clifford R Jack18, Viviana Van Deerlin19, Christopher Randolph20, Iryna V Lobach5, Hilary W Heuer5, Illana Gozes21, Lesley Parker22, Steve Whitaker23, Joe Hirman24, Alistair J Stewart25, Michael Gold26, Bruce H Morimoto27.   

Abstract

BACKGROUND: In preclinical studies, davunetide promoted microtubule stability and reduced tau phosphorylation. Because progressive supranuclear palsy (PSP) is linked to tau pathology, davunetide could be a treatment for PSP. We assessed the safety and efficacy of davunetide in patients with PSP.
METHODS: In a double-blind, parallel group, phase 2/3 trial, participants were randomly assigned with permuted blocks in a 1:1 ratio to davunetide (30 mg twice daily, intranasally) or placebo for 52 weeks at 48 centres in Australia, Canada, France, Germany, the UK, and the USA. Participants met the modified Neuroprotection and Natural History in Parkinson Plus Syndrome study criteria for PSP. Primary endpoints were the change from baseline in PSP Rating Scale (PSPRS) and Schwab and England Activities of Daily Living (SEADL) scale at up to 52 weeks. All participants and study personnel were masked to treatment assignment. Analysis was by intention to treat. The trial is registered with Clinicaltrials.gov, number NCT01110720.
FINDINGS: 313 participants were randomly assigned to davunetide (n=157) or to placebo (n=156), and 241 (77%) completed the study (118 and 156 in the davunetide and placebo groups, respectively). There were no differences in the davunetide and placebo groups in the baseline PSPRS and SEADL. The davunetide and placebo groups did not differ in the change from baseline in PSPRS (median 11·8 [95% CI 10·5 to 13·0] vs 11·8 [10·5 to 13·0], respectively, p=0·41) or SEADL (-0·20 [-0·20 to -0·17] vs -0·20 [-0·22 to -0·17], respectively, p=0·92). 54 serious adverse events were reported in each of the treatment groups, including 11 deaths in the davunetide group and ten in the placebo group. The frequency of nasal adverse events was greater in the davunetide group than in the placebo group (epistaxis 18 [12%] of 156 vs 13 [8%] of 156, rhinorrhoea 15 [10%] vs eight [5%], and nasal discomfort 15 [10%] vs one [<1%]).
INTERPRETATION: Davunetide is not an effective treatment for PSP. Clinical trials of disease-modifying treatment are feasible in patients with PSP and should be pursued with other promising tau-directed treatments. FUNDING: Allon Therapeutics.
Copyright © 2014 Elsevier Ltd. All rights reserved.

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Year:  2014        PMID: 24873720      PMCID: PMC4129545          DOI: 10.1016/S1474-4422(14)70088-2

Source DB:  PubMed          Journal:  Lancet Neurol        ISSN: 1474-4422            Impact factor:   44.182


  32 in total

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