Mamo David, Sedman Ewen, Tillner Joachim, Sellers Edward M, Romach Myroslava K, Kapur Shitij
Department of Psychiatry, University of Toronto, Toronto, Canada.
Psychopharmacology (Berl). 2004 Sep;175(3):382-8. doi: 10.1007/s00213-004-1817-7.
While serotonin 5HT2-receptors have been implicated in the etiology and pharmacological treatment of a number of neuropsychiatric conditions, there are few potent and specific agents available for use in human clinical studies. EMD 281014 is a highly specific 5HT2-receptor antagonist that is currently under development. To find optimal doses for early clinical studies, we conducted a PET study using [18F]setoperone in nine healthy subjects scanned at baseline and following the administration of 1, 3, and 7 mg EMD 281014. The study drug was well tolerated by all study participants, and all doses resulted in > or =70% occupancy at frontal 5HT2-receptors 3 h after drug administration. The data suggest that daily dosing of > or =3 mg EMD 281014 should be sufficient to provide sustained high levels of 5HT2-receptor occupancy in future clinical trials.
虽然血清素5HT2受体与多种神经精神疾病的病因及药物治疗有关,但用于人体临床研究的强效特异性药物却很少。EMD 281014是一种正在研发的高特异性5HT2受体拮抗剂。为了找到早期临床研究的最佳剂量,我们对9名健康受试者进行了一项PET研究,在基线以及给予1、3和7毫克EMD 281014后进行扫描。所有研究参与者对研究药物耐受性良好,给药3小时后,所有剂量在额叶5HT2受体处的占有率均≥70%。数据表明,在未来的临床试验中,每日服用≥3毫克EMD 281014应足以维持较高水平的5HT2受体占有率。