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Rare lung disease and orphan drug development
- Source :
- The Lancet. Respiratory medicine. 1(6)
- Publication Year :
- 2014
-
Abstract
- Summary 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.
- Subjects :
- Pulmonary and Respiratory Medicine
Adult
Lung Diseases
Male
medicine.medical_specialty
Pathology
Delayed Diagnosis
Drug Industry
Orphan Drug Production
Small target
Unnecessary Procedures
Orphan drug
Rare Diseases
Cost of Illness
Terminology as Topic
Drug Discovery
Medicine
Humans
Intensive care medicine
Pharmaceutical industry
Clinical Trials as Topic
business.industry
Health Policy
Self-Help Groups
Incentive
Lung disease
Female
business
Forecasting
Subjects
Details
- ISSN :
- 22132600
- Volume :
- 1
- Issue :
- 6
- Database :
- OpenAIRE
- Journal :
- The Lancet. Respiratory medicine
- Accession number :
- edsair.doi.dedup.....0b8f60d2c3dd57352ab7963561bb8630