Efficacy and safety of aripiprazole vs. haloperidol for long-term maintenance treatment following acute relapse of schizophrenia

Aripiprazole is a novel atypical antipsychotic for the treatment of schizophrenia. It is a D2 receptor partial agonist with partial agonist activity at 5-HT1A receptors and antagonist activity at 5-HT2A receptors. The long-term efficacy and safety of aripiprazole (30 mg/d) relative to haloperidol (1...

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Veröffentlicht in:The international journal of neuropsychopharmacology 2003-12, Vol.6 (4), p.325-337, Article S1461145703003651
Hauptverfasser: Kasper, Siegfried, Lerman, Mark N., McQuade, Robert D., Saha, Anutosh, Carson, William H., Ali, Mirza, Archibald, Donald, Ingenito, Gary, Marcus, Ronald, Pigott, Teresa
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container_issue 4
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container_title The international journal of neuropsychopharmacology
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creator Kasper, Siegfried
Lerman, Mark N.
McQuade, Robert D.
Saha, Anutosh
Carson, William H.
Ali, Mirza
Archibald, Donald
Ingenito, Gary
Marcus, Ronald
Pigott, Teresa
description Aripiprazole is a novel atypical antipsychotic for the treatment of schizophrenia. It is a D2 receptor partial agonist with partial agonist activity at 5-HT1A receptors and antagonist activity at 5-HT2A receptors. The long-term efficacy and safety of aripiprazole (30 mg/d) relative to haloperidol (10 mg/d) were investigated in two 52-wk, randomized, double-blind, multicentre studies (using similar protocols which were prospectively identified to be pooled for analysis) in 1294 patients in acute relapse with a diagnosis of chronic schizophrenia and who had previously responded to antipsychotic medications. Aripiprazole demonstrated long-term efficacy that was comparable or superior to haloperidol across all symptoms measures, including significantly greater improvements for PANSS negative subscale scores and MADRS total score (p
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It is a D2 receptor partial agonist with partial agonist activity at 5-HT1A receptors and antagonist activity at 5-HT2A receptors. The long-term efficacy and safety of aripiprazole (30 mg/d) relative to haloperidol (10 mg/d) were investigated in two 52-wk, randomized, double-blind, multicentre studies (using similar protocols which were prospectively identified to be pooled for analysis) in 1294 patients in acute relapse with a diagnosis of chronic schizophrenia and who had previously responded to antipsychotic medications. Aripiprazole demonstrated long-term efficacy that was comparable or superior to haloperidol across all symptoms measures, including significantly greater improvements for PANSS negative subscale scores and MADRS total score (p&lt;0.05). The time to discontinuation for any reason was significantly greater with aripiprazole than with haloperidol (p=0.0001). Time to discontinuation due to adverse events or lack of efficacy was significantly greater with aripiprazole than with haloperidol (p=0.0001). Aripiprazole was associated with significantly lower scores on all extrapyramidal symptoms assessments than haloperidol (p&lt;0.001). In summary, aripiprazole demonstrated efficacy equivalent or superior to haloperidol with associated benefits for safety and tolerability. 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J. Neuropsychopharm</addtitle><date>2003-12</date><risdate>2003</risdate><volume>6</volume><issue>4</issue><spage>325</spage><epage>337</epage><pages>325-337</pages><artnum>S1461145703003651</artnum><issn>1461-1457</issn><eissn>1469-5111</eissn><abstract>Aripiprazole is a novel atypical antipsychotic for the treatment of schizophrenia. It is a D2 receptor partial agonist with partial agonist activity at 5-HT1A receptors and antagonist activity at 5-HT2A receptors. The long-term efficacy and safety of aripiprazole (30 mg/d) relative to haloperidol (10 mg/d) were investigated in two 52-wk, randomized, double-blind, multicentre studies (using similar protocols which were prospectively identified to be pooled for analysis) in 1294 patients in acute relapse with a diagnosis of chronic schizophrenia and who had previously responded to antipsychotic medications. Aripiprazole demonstrated long-term efficacy that was comparable or superior to haloperidol across all symptoms measures, including significantly greater improvements for PANSS negative subscale scores and MADRS total score (p&lt;0.05). The time to discontinuation for any reason was significantly greater with aripiprazole than with haloperidol (p=0.0001). Time to discontinuation due to adverse events or lack of efficacy was significantly greater with aripiprazole than with haloperidol (p=0.0001). Aripiprazole was associated with significantly lower scores on all extrapyramidal symptoms assessments than haloperidol (p&lt;0.001). In summary, aripiprazole demonstrated efficacy equivalent or superior to haloperidol with associated benefits for safety and tolerability. Aripiprazole represents a promising new option for the long-term treatment of schizophrenia.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><pmid>14609439</pmid><doi>10.1017/S1461145703003651</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1461-1457
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subjects Acute Disease
Adult
Antipsychotic Agents - adverse effects
Antipsychotic Agents - therapeutic use
Aripiprazole
Double-Blind Method
Female
Haloperidol - adverse effects
Haloperidol - therapeutic use
Humans
Long-Term Care
Male
Neurologic Examination - drug effects
Piperazines - adverse effects
Piperazines - therapeutic use
Psychiatric Status Rating Scales
Quinolones - adverse effects
Quinolones - therapeutic use
Recurrence
Schizophrenia - diagnosis
Schizophrenia - drug therapy
Schizophrenic Psychology
Treatment Outcome
title Efficacy and safety of aripiprazole vs. haloperidol for long-term maintenance treatment following acute relapse of schizophrenia
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