Sabril was designated as an orphan drug by the FDA for use in treating infantile spasms.
喜保宁被FDA指定为用于治疗婴儿痉挛的稀少药品。
To obtain orphan drug designation, drugs must be for the treatment, prevention or diagnosis of a rare disease or condition.
孤儿药物审批流程需要该药物可以用于治疗、预防或者诊断罕见疾病。
Orphan drug status provides the company with financial incentives to promote the development of a drug to treat a rare disease or condition.
稀少药品状态提供给药品公司金融鼓励，促使药品公司开发治疗稀少疾病的药物。
Orphan drugs are either drug or biologic products used to treat diseases or conditions affecting fewer than 200,000 people in the United States.
孤儿药物包括药物或者生物制品，用于治疗疾病，并且在美国发病人数少于20万人。
It is our intention to find ways to continue the development of our GVAX Pancreas Vaccine using the benefits conferred by gaining Orphan Drug designation.
Simes说，“我们的目的是利用获得指定的孤儿药物权带来的益处，继续GVAX的研发。”
Orphan drug designation is available for drugs already approved for another disease or condition or for experimental drugs that have not been previously approved.
已经被批准用于其它疾病治疗的药物或者是尚处于试验阶段未被批准的药物都可以通过孤儿药物申报程序进行。
Methods: The historical background formed American Orphan Drug system, regulation of Orphan Drug system, preferential measure, and FDA s approval procedure are stated.
方法：根据个人掌握的资料，说明美国罕见病药物制度形成的背景、有关法规、优惠措施及FDA审批程序。
ABSTRACT: OBJECTIVE: to introduce high-value drug insurance access mechanism in Australia, and to provide suggestion for improving orphan drug medical insurance access in China.
摘要：目的：介绍澳大利亚高值药物医保准入机制，为我国罕用药医保准入的完善提供建议。
The main difficulties of Orphan Drug Research and Development is by both sides, on the one hand, the small number of patients, limited commercial value, on the other hand, insufficient cases.
罕用药研发主要面对两方面的困难，一方面是病患人数少，商业价值有限，另一方面是病例不足。
During the workshop, participants will propose a specific drug for a specific rare disease and work on an orphan designation application to submit to the FDA at the conclusion of the workshop.
研讨会期间，与会者将提出一个具体的孤儿药物按照FDA的孤儿药物审批过程进行研讨，并将其申请提交给FDA作为研讨会的总结。
During the workshop, participants will propose a specific drug for a specific rare disease and work on an orphan designation application to submit to the FDA at the conclusion of the workshop.
研讨会期间，与会者将提出一个具体的孤儿药物按照FDA的孤儿药物审批过程进行研讨，并将其申请提交给FDA作为研讨会的总结。
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