TY - JOUR
T1 - A randomized, double blind, placebo-controlled trial of pioglitazone in combination with riluzole in amyotrophic lateral sclerosis
AU - Dupuis, Luc
AU - Dengler, Reinhard
AU - Heneka, Michael T.
AU - Meyer, Thomas
AU - Zierz, Stephan
AU - Kassubek, Jan
AU - Fischer, Wilhelm
AU - Steiner, Franziska
AU - Lindauer, Eva
AU - Otto, Markus
AU - Dreyhaupt, Jens
AU - Grehl, Torsten
AU - Hermann, Andreas
AU - Winkler, Andrea S.
AU - Bogdahn, Ulrich
AU - Benecke, Reiner
AU - Schrank, Bertold
AU - Wessig, Carsten
AU - Grosskreutz, Julian
AU - Ludolph, Albert C.
AU - The GERP ALS Study Group, GERP ALS Study Group
PY - 2012/6/8
Y1 - 2012/6/8
N2 - Background: Pioglitazone, an oral anti-diabetic that stimulates the PPAR-gamma transcription factor, increased survival of mice with amyotrophic lateral sclerosis (ALS). Methods/Principal Findings: We performed a phase II, double blind, multicentre, placebo controlled trial of pioglitazone in ALS patients under riluzole. 219 patients were randomly assigned to receive 45 mg/day of pioglitazone or placebo (one: one allocation ratio). The primary endpoint was survival. Secondary endpoints included incidence of non-invasive ventilation and tracheotomy, and slopes of ALS-FRS, slow vital capacity, and quality of life as assessed using EUROQoL EQ-5D. The study was conducted under a two-stage group sequential test, allowing to stop for futility or superiority after interim analysis. Shortly after interim analysis, 30 patients under pioglitazone and 24 patients under placebo had died. The trial was stopped for futility; the hazard ratio for primary endpoint was 1.21 (95% CI: 0.71-2.07, p = 0.48). Secondary endpoints were not modified by pioglitazone treatment. Pioglitazone was well tolerated. Conclusion/Significance: Pioglitazone has no beneficial effects on the survival of ALS patients as add-on therapy to riluzole.
AB - Background: Pioglitazone, an oral anti-diabetic that stimulates the PPAR-gamma transcription factor, increased survival of mice with amyotrophic lateral sclerosis (ALS). Methods/Principal Findings: We performed a phase II, double blind, multicentre, placebo controlled trial of pioglitazone in ALS patients under riluzole. 219 patients were randomly assigned to receive 45 mg/day of pioglitazone or placebo (one: one allocation ratio). The primary endpoint was survival. Secondary endpoints included incidence of non-invasive ventilation and tracheotomy, and slopes of ALS-FRS, slow vital capacity, and quality of life as assessed using EUROQoL EQ-5D. The study was conducted under a two-stage group sequential test, allowing to stop for futility or superiority after interim analysis. Shortly after interim analysis, 30 patients under pioglitazone and 24 patients under placebo had died. The trial was stopped for futility; the hazard ratio for primary endpoint was 1.21 (95% CI: 0.71-2.07, p = 0.48). Secondary endpoints were not modified by pioglitazone treatment. Pioglitazone was well tolerated. Conclusion/Significance: Pioglitazone has no beneficial effects on the survival of ALS patients as add-on therapy to riluzole.
UR - http://www.scopus.com/inward/record.url?scp=84862010340&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0037885
DO - 10.1371/journal.pone.0037885
M3 - Journal articles
C2 - 22715372
AN - SCOPUS:84862010340
VL - 7
JO - PLoS ONE
JF - PLoS ONE
IS - 6
M1 - e37885
ER -