Rioux P
Variagenics Inc, Cambridge, MA 02139-1562, USA.
IDrugs. 1999 Feb;2(2):153-67.
CAMPATH-1H, a T-cell-depleting, humanized monoclonal antibody, is under development by LeukoSite and ILEX for the potential treatment of chronic lymphocytic leukemia (CLL). In August 1998, ILEX completed enrollment of a pivotal clinical trial of CAMPATH-1H in the treatment of CLL. The study has enrolled 94 patients at 20 centers in the US and Europe. It is anticipated that achievement of the target response would result in a biologics license application being filed with the FDA in mid-1999. Preliminary unaudited results reported by one of the clinical sites were positive. Additional potential therapeutic areas include vasculitis and multiple sclerosis. Preliminary studies have also shown the antibody may reverse acute renal transplant rejection episodes and be useful in ex vivo purging of bone marrow to remove potentially malignant cells. The US FDA has granted Fast Track designation to CAMPATH. The product has orphan drug status.
坎帕昔单抗-1H是一种耗竭T细胞的人源化单克隆抗体,由LeukoSite公司和ILEX公司共同研发,用于潜在治疗慢性淋巴细胞白血病(CLL)。1998年8月,ILEX完成了坎帕昔单抗-1H治疗CLL的关键临床试验的患者入组工作。该研究在美国和欧洲的20个中心招募了94名患者。预计达到目标反应后,将于1999年年中向美国食品药品监督管理局(FDA)提交生物制品许可申请。其中一个临床研究点报告的未经审计的初步结果呈阳性。其他潜在治疗领域包括血管炎和多发性硬化症。初步研究还表明,该抗体可能逆转急性肾移植排斥反应,并且在体外清除骨髓中潜在的恶性细胞方面有用。美国FDA已授予坎帕昔单抗快速通道指定。该产品具有孤儿药地位。