While drug discovery for common disorders is somewhat standard and based on the large potential markets, the small market for most orphan diseases means that effective therapies are uncommon. With next generation DNA sequencing, the pace of inherited novel rare disease gene identification has increased markedly. Drug discovery for rare diseases is somewhat hampered by a lack of collaboration between academia and industry separating the necessary resources from skills. This volume discusses important aspects of orphan drug development such as regulatory affairs, public industry partnership, bench to bedside using examples of rare diseases, challenges of clinical trials and future directions.
Rare diseases collectively affect millions of Americans of all ages, but developing drugs and medical devices to prevent, diagnose, and treat these conditions is challenging.
Often, the disease process manifested in a certain rare disease is strikingly similar to the disease process observed in a common disease. This work ties the lessons learned about rare diseases to our understanding of common ones.
This book provides an up-to-date monograph on the drug discovery and regulatory elements of therapeutics used to treat rare or "orphan" diseases.
Orphan Diseases and Orphan Drugs
Orphan Drug Law Matures into Medical Mainstay
Global Pediatric Development of Drugs, Biologics, and Medical Devices
Orphan Drug Reauthorization: Hearing Before the Subcommittee on Health and the Environment of the Committee on Energy and Commerce, House...
According to Sidney Wolfe , a physician and well - known consumer advocate , the prevalence of doctor - bribing and acquisition of bogus clinical data through large pay - offs is higher than most people believe . Wolfe described several ...
Orphan Drugs
Food and Drug Administration's Review Process for Products to Treat Rare Diseases and Neglected Tropical Diseases: Hearing Before a Subcommittee...