Hacksell Uli, Burstein Ethan S, McFarland Krista, Mills Roger G, Williams Hilde
ACADIA Pharmaceuticals Inc., 11085 Torreyana Road, Ste. 100, San Diego, CA, 92121, USA,
Neurochem Res. 2014 Oct;39(10):2008-17. doi: 10.1007/s11064-014-1293-3. Epub 2014 Mar 30.
Parkinson's disease psychosis (PDP) is a condition that may develop in up to 60 % of Parkinson's patients, and is a major reason for nursing home placement for those affected. There are no FDA approved drugs for PDP but low doses of atypical anti-psychotic drugs (APDs) are commonly prescribed off-label. Only low-dose clozapine has shown efficacy in randomized controlled trials, but all APDs have black box warnings related to the increased mortality and morbidity when used in elderly demented patients. Using molecular pharmacological profiling of a large collection of marketed drugs, we discovered that potent inverse agonist activity against 5-HT2A serotonin receptors was a common feature of atypical APDs, especially the atypical APDs used to treat PDP. Since low-dose clozapine therapy selectively blocks this receptor, it was hypothesized that a highly selective 5-HT2A receptor inverse agonist might provide good symptom control in patients suffering from PDP, with a greatly improved safety and tolerability profile. A high throughput screening and subsequent chemical lead optimization campaign to develop potent, selective 5-HT2A receptor inverse agonists was launched, eventually resulting in the discovery of pimavanserin. Pimavanserin displays nanomolar potency as a 5-HT2A receptor inverse agonist, selectivity for 5-HT2A over 5-HT2C receptors, and no meaningful activity at any other G-protein coupled receptor. It demonstrated robust activity in preclinical models of schizophrenia and PDP, and did not worsen motoric symptoms, in contrast to the APDs tested. In a Phase III clinical trial, pimavanserin showed highly significant benefits in the primary endpoint, the scale for assessment of positive symptoms-PD, a scale adapted for use in PDP. In addition, improvements in all other efficacy endpoints, including physician's clinical global impression, caregiver burden, night-time sleep quality and daytime wakefulness, were seen. Pimavanserin demonstrated good safety and tolerability and did not worsen motoric symptoms as assessed by the unified Parkinson's disease rating scale parts II and III. An open-label extension study has further demonstrated that pimavanserin is safe and well-tolerated with long-term use. Pimavanserin may therefore offer a viable treatment option for patients suffering from PDP.
帕金森病精神病(PDP)是一种在高达60%的帕金森病患者中可能出现的病症,是患者入住疗养院的主要原因。目前尚无美国食品药品监督管理局(FDA)批准用于治疗PDP的药物,但低剂量的非典型抗精神病药物(APD)通常被超适应证处方使用。只有低剂量氯氮平在随机对照试验中显示出疗效,但所有APD都有黑框警告,提示在老年痴呆患者中使用会增加死亡率和发病率。通过对大量市售药物进行分子药理学分析,我们发现对5-HT2A血清素受体具有强效反向激动剂活性是非典型APD的一个共同特征,尤其是用于治疗PDP的非典型APD。由于低剂量氯氮平疗法可选择性阻断该受体,因此推测一种高选择性5-HT2A受体反向激动剂可能在PDP患者中提供良好的症状控制,同时安全性和耐受性有极大改善。于是开展了一项高通量筛选及后续化学先导物优化活动,以开发强效、选择性的5-HT2A受体反向激动剂,最终发现了匹莫范色林。匹莫范色林作为5-HT2A受体反向激动剂表现出纳摩尔级别的效力,对5-HT2A的选择性高于5-HT2C受体,并且在任何其他G蛋白偶联受体上均无显著活性。与所测试的APD相比,它在精神分裂症和PDP的临床前模型中表现出强大活性,且不会加重运动症状。在一项III期临床试验中,匹莫范色林在主要终点指标——用于评估PDP阳性症状的量表(为适用于PDP而改编)上显示出极为显著的益处。此外,在所有其他疗效终点指标上均有改善,包括医生的临床整体印象、照料者负担、夜间睡眠质量和白天清醒程度。匹莫范色林表现出良好的安全性和耐受性,根据统一帕金森病评定量表第二部分和第三部分评估,它不会加重运动症状。一项开放标签扩展研究进一步证明,匹莫范色林长期使用安全且耐受性良好。因此,匹莫范色林可能为PDP患者提供一种可行的治疗选择。