Galeffi C
Laboratorio di Chimica del Farmaco, Istituto Superiore di Sanità, Roma.
Ann Ist Super Sanita. 1991;27(2):341-3.
Diseases lacking in satisfactory therapies, named orphans (over 60% of the known), raise the problem of the availability of new drugs to be discovered and evaluated on toxicological and clinical bases. The estimated cost for the full development of a drug makes it not profitable (and therefore orphan drug) in the case of rare diseases and the typical diseases of developing countries. The USA with the Orphan Drug Act have faced the former, whereas WHO with the "Tropical Diseases Research" programme has faced the latter. Uncommon formulations and dosages of known substances and products no longer marketed as non-profitable are considered orphans drugs as well.
缺乏令人满意治疗方法的疾病,即所谓的罕见病(已知疾病的60%以上),引发了基于毒理学和临床研究发现并评估新药的可及性问题。对于罕见病以及发展中国家的典型疾病而言,研发一种药物的预估成本使得其无利可图(因此属于孤儿药)。美国通过《孤儿药法案》应对了前者,而世界卫生组织通过“热带病研究”项目应对了后者。已知物质和产品不再作为盈利产品销售的不常见剂型和剂量也被视为孤儿药。