Efficacy and safety of aripiprazole and haloperidol versus placebo in patients with schizophrenia and schizoaffective disorder

被引:487
作者
Kane, JM
Carson, WH
Saha, AR
McQuade, RD
Ingenito, GG
Zimbroff, DL
Ali, MW
机构
[1] Pacific Clin Res, San Bernardino, CA USA
[2] Bristol Myers Squibb Co, Lawrenceville, NJ USA
[3] Otsuka Maryland Res Inst, Rockville, MD USA
[4] Bristol Myers Squibb Co, Wallingford, CT 06492 USA
[5] ZuckerHillside Hosp, Glen Oaks, NY USA
关键词
D O I
10.4088/JCP.v63n0903
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background: Aripiprazole is an investigational agent for treating schizophrenia that has a novel pharmacologic profile. The present study investigated the efficacy, safety, and tolerability of aripiprazole and haloperidol compared with placebo. Method: A 4-week, double-blind, randomized study, conducted at 36 U.S. centers between July 1997 and June 1998, compared aripiprazole (15 mg/day, 30 mg/day) to placebo, with haloperidol (10 mg/day) as an active control. Fixed doses of each agent were administered from day 1 throughout the study. A total of 414 patients with a primary DSM-IV diagnosis of schizophrenia or schizoaffective disorder were randomized. Efficacy measures included the Positive and Negative Syndrome Scale (PANSS) total, PANSS positive, PANSS negative, PANSS-derived Brief Psychiatric Rating Scale (BPRS) core, Clinical Global Impressions (CGI)Severity of Illness, and mean CGI-Improvement scores. Safety and tolerability evaluations included extrapyramidal symptoms (EPS), weight gain, serum prolactin level, and QTc interval. Results: Both doses of aripiprazole and haloperidol, 10 mg, produced statistically significant (p 5.05) improvements from baseline in PANSS total, PANSS positive, PANSS-derived BPRS core, and CGI-Severity scores and significantly lower CGI-Improvement scores at endpoint, compared with placebo. Aripiprazole, 15 mg, and haloperidol, 10 mg, significantly improved PANSS negative score compared with placebo. Both aripiprazole doses and haloperidol separated from placebo for PANSS total scores at week 2. Unlike haloperidol, aripiprazole was not associated with significant EPS or prolactin elevation at endpoint compared with placebo. There were no statistically significant differences in mean changes in body weight across the treatment groups versus placebo, and no patients receiving aripiprazole experienced clinically significant increases in QTc interval. Conclusion: Aripiprazole, effective against positive and negative symptoms, is a safe and well-tolerated potential treatment for schizophrenia and schizoaffective disorder.
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收藏
页码:763 / 771
页数:9
相关论文
共 37 条
  • [1] *ABN INV MOV SCAL, 1976, 76338 US DHEW PUBL, P534
  • [2] Allison DB, 2001, J CLIN PSYCHIAT, V62, P22
  • [3] RECEPTOR ACTIVITY AND TURNOVER OF DOPAMINE AND NORADRENALINE AFTER NEUROLEPTICS
    ANDEN, NE
    BUTCHER, SG
    CORRODI, H
    FUXE, K
    UNGERSTEDT, U
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1970, 11 (03) : 303 - +
  • [4] A RATING-SCALE FOR DRUG-INDUCED AKATHISIA
    BARNES, TRE
    [J]. BRITISH JOURNAL OF PSYCHIATRY, 1989, 154 : 672 - 676
  • [5] BUNNEY WE, 1995, CLIN NEUROSCI, V3, P55
  • [6] Aripiprazole, a novel antipsychotic, is a high-affinity partial agonist at human dopamine D2 receptors
    Burris, KD
    Molski, TF
    Xu, C
    Ryan, E
    Tottori, K
    Kikuchi, T
    Yocca, FD
    Molinoff, PB
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 302 (01) : 381 - 389
  • [7] Network interactions in schizophrenia - therapeutic implications
    Carlsson, A
    Waters, N
    Waters, S
    Carlsson, ML
    [J]. BRAIN RESEARCH REVIEWS, 2000, 31 (2-3) : 342 - 349
  • [8] THE CURRENT STATUS OF THE DOPAMINE HYPOTHESIS OF SCHIZOPHRENIA
    CARLSSON, A
    [J]. NEUROPSYCHOPHARMACOLOGY, 1988, 1 (03) : 179 - 186
  • [9] Carson WH, 2001, SCHIZOPHR RES, V49, P221
  • [10] *CLIN GLOB IMPRESS, 1976, 76338 DHEW ADM, P218