Goldman D P, Clarke A E, Garber A M
Stanford University.
Int J Technol Assess Health Care. 1992 Fall;8(4):583-97. doi: 10.1017/s0266462300002294.
The FDA recently approved Ceredase, a new treatment for Gaucher's disease, under the provisions of the Orphan Drug Act. Ceredase is unusually expensive, but there are no satisfactory alternative therapies. It appears likely that Ceredase would not have become available without the protection of the Orphan Drug Act, but its expense and the lack of information about its long-term effects on health raise questions about whether the ODA provides appropriate incentives to develop cost-effective technologies.
美国食品药品监督管理局(FDA)最近依据《孤儿药法案》的条款批准了一种用于治疗戈谢病的新疗法——思而赞(Ceredase)。思而赞价格异常昂贵,但目前尚无令人满意的替代疗法。若没有《孤儿药法案》的保护,思而赞似乎不太可能问世,但其高昂的费用以及缺乏关于其对健康长期影响的信息引发了人们对《孤儿药法案》是否为开发具有成本效益的技术提供了适当激励措施的质疑。