Sipe Jack C
Department of Molecular and Experimental Medicine, The Scripps Research Institute, and Scripps Clinic, 10550 North Torrey Pines Road (MEM-215), LaJolla, CA 92037 USA.
Expert Rev Neurother. 2005 Nov;5(6):721-7. doi: 10.1586/14737175.5.6.721.
In the 1990s, cladribine was developed as an adenosine deaminase-resistant nucleoside analog with selective lymphotoxic specificity in the hope that it might become useful in the treatment of some lymphoid neoplasms and autoimmune disorders. Several clinical trials demonstrated very significant effectiveness and safety of cladribine in the cure of hairy-cell leukemia, and the control of many other lymphoid malignancies. Cladribine was also extensively tested in selected autoimmune disorders, most notably in multiple sclerosis, with evidence of efficacy, tolerability and acceptable side effects/toxicity. The previous clinical studies and current status of cladribine for the treatment of multiple sclerosis are considered in this drug profile. In January 2005, Serono and IVAX announced plans to initiate a Phase III study of a specially formulated oral tablet of cladribine (Mylinax, Serono and IVAX) for the treatment of relapsing forms of multiple sclerosis. The proposed study will be the first large multicenter randomized controlled clinical trial of oral cladribine in multiple sclerosis.
20世纪90年代,克拉屈滨作为一种对腺苷脱氨酶有抗性的核苷类似物被研发出来,它具有选择性淋巴细胞毒性特异性,人们希望它能在某些淋巴瘤和自身免疫性疾病的治疗中发挥作用。多项临床试验证明,克拉屈滨在治疗毛细胞白血病以及控制许多其他淋巴瘤方面具有显著的有效性和安全性。克拉屈滨也在特定的自身免疫性疾病中进行了广泛测试,最显著的是在多发性硬化症中,有证据表明其具有疗效、耐受性且副作用/毒性可接受。本药物简介将探讨克拉屈滨治疗多发性硬化症的既往临床研究及现状。2005年1月,雪兰诺公司和IVAX公司宣布计划启动一项关于克拉屈滨特制口服片剂(Mylinax,雪兰诺公司和IVAX公司)治疗复发型多发性硬化症的III期研究。拟进行的这项研究将是口服克拉屈滨治疗多发性硬化症的首个大型多中心随机对照临床试验。