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罕见肺部疾病与孤儿药研发。

Rare lung disease and orphan drug development.

机构信息

Centre for Rare Lung Diseases, Department of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Modena, Italy.

Imperial College, London, UK.

出版信息

Lancet Respir Med. 2013 Aug;1(6):479-87. doi: 10.1016/S2213-2600(13)70085-7. Epub 2013 Jun 25.

Abstract

Rare diseases are a major health-care burden worldwide. Very little is known about the cause, behaviour, and treatment of these disorders, and thus non-specialist health-care providers and patients are left without sufficient knowledge to manage these diseases. Up to 3 million Europeans are estimated to have a rare lung disease. Several organisations-many of which are patient led-attempt to raise the profile of rare lung diseases to improve understanding and management of these disorders. Incentives have now been introduced in the USA and Europe that encourage the pharmaceutical industry to invest in targets that might otherwise not appeal because of small target populations. Despite many intrinsic challenges and obstacles, considerable progress is constantly being made in the research and development of drugs for rare disorders.

摘要

罕见病是全球范围内的一个主要医疗保健负担。对于这些疾病的病因、表现和治疗方法,我们知之甚少,因此非专业的医疗保健提供者和患者缺乏足够的知识来管理这些疾病。据估计,多达 300 万欧洲人患有罕见的肺部疾病。许多组织(其中许多是由患者领导的)试图提高罕见肺部疾病的知名度,以改善对这些疾病的理解和管理。美国和欧洲现在已经出台了激励措施,鼓励制药行业投资于那些由于目标人群较小而可能没有吸引力的靶点。尽管面临许多内在的挑战和障碍,但在罕见疾病药物的研发方面,不断取得相当大的进展。

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