Geerts Hugo
In Silico Biosciences Inc, 686 Westwind Drive, Berwyn, PA 19104, USA.
IDrugs. 2007 Feb;10(2):121-33.
(R)-flurbiprofen, the R-enantiomer of racemic flurbiprofen, is undergoing development by Myriad Genetics Inc, under license from Encore Pharmaceuticals Inc, for the potential treatment of Alzheimer's disease (AD). Devoid of any direct cyclooxygenase inhibition, which is associated with the more toxic S-enantiomer of flurbiprofen, (R)-flurbiprofen appears to modulate gamma-secretase, the enzyme that cleaves the C-terminal portion of the malignant Abeta(1-42) peptide out of amyloid precursor protein. In murine models of AD, (R)-flurbiprofen lowered brain levels of Abeta(1-42), and chronic dosing reduced brain amyloid pathology and prevented defects in learning and memory. In a phase II clinical trial in AD, (R)-flurbiprofen was determined to be most effective in a subset of patients who had high blood concentrations of the drug (> 75 microg/ml). These patients demonstrated a benefit in cognitive and behavioral performance that ranged from 36 to 48%, and statistical significance was achieved for two out of three trial endpoints. Compared with placebo, (R)-flurbiprofen also significantly reduced the incidence of psychiatric problems and the average time to a first psychiatric incidence. (R)-flurbiprofen has been generally well tolerated at high doses in clinical trials. Two pivotal phase III clinical trials in AD are underway in more than 2400 patients. The compound had also been under development for the treatment of prostate cancer; however, this indication was discontinued after disappointing phase IIa trial results.
(R)-氟比洛芬是消旋氟比洛芬的R-对映体,由Myriad Genetics公司根据与Encore制药公司的许可进行开发,用于潜在治疗阿尔茨海默病(AD)。(R)-氟比洛芬没有任何直接的环氧化酶抑制作用,而这种作用与氟比洛芬毒性更强的S-对映体有关,它似乎能调节γ-分泌酶,该酶可从淀粉样前体蛋白中切割出恶性β-淀粉样蛋白(1-42)肽的C末端部分。在AD的小鼠模型中,(R)-氟比洛芬降低了大脑中β-淀粉样蛋白(1-42)的水平,长期给药可减轻大脑淀粉样病变,并预防学习和记忆缺陷。在一项AD的II期临床试验中,(R)-氟比洛芬被确定在药物血药浓度高(>75微克/毫升)的一部分患者中最有效。这些患者在认知和行为表现方面的获益范围为36%至48%,三项试验终点中有两项达到统计学意义。与安慰剂相比,(R)-氟比洛芬还显著降低了精神问题的发生率以及首次发生精神问题的平均时间。在临床试验中,(R)-氟比洛芬在高剂量下总体耐受性良好。两项针对AD的关键III期临床试验正在2400多名患者中进行。该化合物也曾被开发用于治疗前列腺癌;然而,在IIa期试验结果令人失望后,该适应症已被停止。