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Once-daily controlled release remoxipride is equieffective with twice-daily immediate release remoxipride in the treatment of schizophreniaDepartment of Psychiatry, St. James's University Hospital, Leeds LS9 7TF
7 Hungerford Road, Huddersfield HD3 3AL
Department of Psychiatry, The General Hospital, Halifax HX3 OPW
Department of General Psychiatry and Psychogeriatrics, De La Pole Hospital, Willerby, Hull HU10 6ED
Department of Psychiatry, Stanley Royd Hospital, Wakefield WF14 4DQ, UK
Astra Arcus AB, S-15185 Södertälje, Sweden
Department of Clinical Research, Astra Pharmaceuticals Ltd., Kings Langley WD4 8DH, UK
A controlled release (CR) formulation of remoxipride (Roxiam®, Astra) given once-daily was compared to immediate release (IR) remoxipride given twice-daily, with respect to efficacy and tolerability, in a 4-week multicentre parallel-group dose titration (200-600 mg/day) study with acutely ill schizophrenic patients. Forty- three patients received remoxipride CR (mean dose 344 mg/day) and 49 patients received remoxipride IR (mean dose 346 mg/day). Efficacy was assessed using the Kolakowska version of the Brief Psychiatric Rating Scale (BPRS score of
Key Words: remoxipride schizophrenia controlled release antipsychotic once-daily
Journal of Psychopharmacology, Vol. 7, No. 3,
276-282 (1993) |
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18 points at entry) and the Clinical Global Impression scale (CGI), while extrapyramidal symptoms were rated using the Simpson and Angus scale. Both formulations of remoxipride produced clinical improvement, with the BPRS median total score falling from 35 at baseline to 16 at last rating in the remoxipride CR group, and from 33 to 12.5 in the remoxipride IR group. More than 70% of the patients in both groups were assessed as 'much improved' or 'very much improved' according to the CGI scale. Both formulations of remoxipride were well-tolerated, with a low incidence of treatment-emergent adverse symptoms, including extrapyramidal side effects. No statistically significant differences were detected between the treatment groups with regard to efficacy, safety or tolerability.