Stangel M, Moharregh-Khiabani D, Linker R A, Gold R
Klink für Neurologie, Medizinische Hochschule Hannover, Carl-Neuberg-Strasse 1, Hannover, Germany.
Nervenarzt. 2008 Feb;79(2):212-7. doi: 10.1007/s00115-007-2378-x.
The currently licensed medications for relapsing-remitting multiple sclerosis (RRMS) are only partially effective and require a parenteral route of administration. Thus there is a need for new, preferably orally available therapeutics. Such a substance could be fumaric acid and its esters (FAE). These compounds are already in use for treatment of psoriasis and are known to have an immunomodulatory effect. In addition there is a potential for neuroprotective effects as suggested by in vitro studies and experiments in the animal model of experimental autoimmune encephalomyelitis. A phase II clinical study in RRMS patients with the modified fumaric acid ester BG-12 showed as "proof of principle" in a frequent MRI design that FAE significantly reduce the number of gadolinium-enhancing lesions after 24 weeks of treatment. Further phase III studies have been started to explore the long-term efficacy of this substance. The results of these studies will show if FAE can be another treatment option, maybe for combination therapy, in patients with MS.
目前用于复发缓解型多发性硬化症(RRMS)的获批药物仅部分有效,且需要肠胃外给药途径。因此,需要新型的、最好是口服可用的治疗药物。富马酸及其酯类(FAE)可能就是这样一种物质。这些化合物已用于治疗银屑病,并且已知具有免疫调节作用。此外,体外研究和实验性自身免疫性脑脊髓炎动物模型实验表明,它们还具有神经保护作用的潜力。一项针对RRMS患者的II期临床研究使用改良富马酸酯BG-12,在一项频繁MRI设计中作为“原理验证”表明,FAE在治疗24周后可显著减少钆增强病灶的数量。进一步的III期研究已经启动,以探索该物质的长期疗效。这些研究结果将表明FAE是否可以成为MS患者的另一种治疗选择,或许可用于联合治疗。