Publication
Rasagiline as an adjunct to levodopa in patients with Parkinson's disease and motor fluctuations (LARGO, Lasting effect in Adjunct therapy with Rasagiline Given Once daily, study): a randomised, double-blind, parallel-group trial.
dc.contributor.author | Rascol, O. | |
dc.contributor.author | Brooks, D.J. | |
dc.contributor.author | Melamed, E. | |
dc.contributor.author | Oertel, W. | |
dc.contributor.author | Poewe, W. | |
dc.contributor.author | Stocchi, F. | |
dc.contributor.author | Tolosa, E. | |
dc.contributor.author | LARGO study group | |
dc.date.accessioned | 2010-08-18T14:09:52Z | |
dc.date.available | 2010-08-18T14:09:52Z | |
dc.date.issued | 2005-03 | |
dc.description.abstract | Lancet. 2005 Mar 12-18;365(9463):947-54. Rasagiline as an adjunct to levodopa in patients with Parkinson's disease and motor fluctuations (LARGO, Lasting effect in Adjunct therapy with Rasagiline Given Once daily, study): a randomised, double-blind, parallel-group trial. Rascol O, Brooks DJ, Melamed E, Oertel W, Poewe W, Stocchi F, Tolosa E; LARGO study group. Clinical Investigation Centre, Department of Clinical Pharmacology, University Hospital, Toulouse, France. rascol@cict.fr Comment in: • Lancet. 2005 Mar 12-18;365(9463):914-6. Abstract BACKGROUND: Rasagiline mesylate is a novel drug for Parkinson's disease with selective, irreversible monoamine oxidase B (MAO-B) inhibitor activity, and is effective as monotherapy in early disease. This study investigated rasagiline efficacy and safety in levodopa-treated patients with Parkinson's disease and motor fluctuations. METHODS: In an 18-week, double-blind, multicentre (74 hospitals and academic centres in Israel, Argentina, and Europe) trial, 687 outpatients were randomly assigned to oral rasagiline (231 individuals; 1 mg once daily), entacapone (227; 200 mg with every levodopa dose), or placebo (229). Primary outcome was change in total daily off-time (intention-to-treat population). Other measures included the clinical global improvement (CGI) score and unified Parkinson's disease rating scale (UPDRS) scores. Analysis was by intention to treat. FINDINGS: 88 (13%) patients who were assigned treatment did not complete the study (23 rasagiline, 30 entacapone, 35 placebo), mainly because of withdrawal of consent (n=34) and adverse events (n=34). Both rasagiline and entacapone reduced mean daily off-time (-1.18 h rasagiline and -1.2 h entacapone vs placebo -0.4 h; p=0.0001, p<0.0001, respectively) and increased daily on-time without troublesome dyskinesia (0.85 h vs placebo 0.03 h; p=0.0005 for both). We recorded significant mean improvements in CGI scores (-0.86 rasagiline and -0.72 entacapone vs -0.37 placebo; p<0.0001, p=0.0002, respectively). Changes in UPDRS scores also significantly improved for activities of daily living during off-time (-1.71 and -1.38 vs placebo; p<0.0001, p=0.0006, respectively) and motor function during on-time (-2.94 and -2.73 vs placebo; both p<0.0001). Frequency of adverse events was similar for all treatments. INTERPRETATION: Once-daily rasagiline reduces mean daily off-time and improves symptoms of Parkinson's disease in levodopa-treated patients with motor fluctuations, an effect similar to that of entacapone. PMID: 15766996 [PubMed - indexed for MEDLINE | por |
dc.identifier.issn | 0140-6736 | |
dc.identifier.uri | http://hdl.handle.net/10400.16/429 | |
dc.language.iso | eng | por |
dc.publisher | Elsevier | por |
dc.relation.ispartofseries | 365; | |
dc.relation.publisherversion | http://www.thelancet.com | por |
dc.title | Rasagiline as an adjunct to levodopa in patients with Parkinson's disease and motor fluctuations (LARGO, Lasting effect in Adjunct therapy with Rasagiline Given Once daily, study): a randomised, double-blind, parallel-group trial. | por |
dc.type | journal article | |
dspace.entity.type | Publication | |
oaire.citation.conferencePlace | London | por |
oaire.citation.title | The Lancet | por |
rcaap.rights | openAccess | por |
rcaap.type | article | por |