Cariprazine, an orally active D2/D3 receptor antagonist, for the potential treatment of schizophrenia, bipolar mania and depression.

Gerhard Gründer
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Abstract

Cariprazine (RGH-188), which is being codeveloped by Gedeon Richter Ltd, Forest Laboratories Inc and Mitsubishi Tanabe Pharma Corp, is a novel putative antipsychotic drug that exerts partial agonism at dopamine D2/D3 receptors, with preferential binding to D3 receptors, and partial agonism at serotonin 5-HT1A receptors. Its activity at D2/D3 receptors may be lower than that of the prototype partial agonist aripiprazole. The antipsychotic activity of cariprazine was demonstrated in animal models, and data also suggest that the propensity for extrapyramidal side effects is low and that the drug may have procognitive properties. Cariprazine is rapidly absorbed, with high oral bioavailability and a long plasma elimination t1/2. Cariprazine is in phase III clinical trials in patients with schizophrenia and in patients with bipolar disorder. Data from phase II trials in patients with schizophrenia and bipolar mania indicate that the drug has antipsychotic and antimanic properties that are superior to placebo. With its unique receptor affinity profile, cariprazine may represent a potential enrichment of the therapeutic armamentarium for schizophrenia and affective disorders. Its activity against the cognitive deficits associated with schizophrenia has to be carefully investigated.

Cariprazine,一种口服D2/D3受体拮抗剂,用于治疗精神分裂症、双相躁狂症和抑郁症。
Cariprazine (RGH-188)是由Gedeon Richter Ltd, Forest Laboratories Inc和Mitsubishi Tanabe Pharma Corp共同开发的一种新型抗精神病药物,可对多巴胺D2/D3受体产生部分激动作用,优先结合D3受体,并对血清素5-HT1A受体产生部分激动作用。它对D2/D3受体的活性可能低于原型部分激动剂阿立哌唑。cariprazine的抗精神病活性在动物模型中得到证实,数据还表明,锥体外系副作用的倾向很低,并且该药物可能具有促进认知的特性。卡吡嗪吸收迅速,口服生物利用度高,血浆消除时间长1/2。Cariprazine正处于精神分裂症和双相情感障碍患者的III期临床试验中。在精神分裂症和双相躁狂症患者中进行的II期试验数据表明,该药具有优于安慰剂的抗精神病和抗躁狂特性。由于其独特的受体亲和性,卡吡嗪可能代表了精神分裂症和情感性障碍的潜在丰富治疗手段。它对与精神分裂症相关的认知缺陷的作用必须仔细研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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