Rare diseases, when taken together, are not that rare at all. According to the National Institutes of Health (NIH), 30 million Americans, or 10 percent of the population, have one of the approximately 7,000 known rare diseases. A disease is defined as a rare or orphan disease when it affects fewer than 200,000 people in the United States.
We’ve seen incredible advances in the development of medicines to treat patients with rare diseases as researchers uncover the molecular and genomic drivers of many conditions. Rare diseases are biologically complex and scientists are working hard to uncover the underlying causes and the clinical course of individual rare diseases. America’s biopharmaceutical researchers are leveraging new technologies and the growing understanding of the genetic basis for many rare diseases to develop groundbreaking therapies to meet this unmet need.
Biopharmaceutical industry researchers continue are making progress in the fight against rare diseases as innovative science has opened new opportunities. Today, there are and more than 700 medicines are in the current biopharmaceutical pipeline.
Despite recent progress, there is still much more work to be done. In fact, less than 10% of rare diseases have an approved treatment option.
Developing medicines to treat rare diseases presents scientific and operational challenges. The complex biology of many rare diseases presents unique hurdles for scientists, making it difficult to design and implement a drug development program. Within a particular rare disease, there can be many variations or subtypes resulting in different clinical manifestations and disease progressions. Additionally, due to the inherently small population of patients with a rare disease, recruiting for and conducting clinical trials can be difficult.
Despite these challenges, America’s biopharmaceutical researchers have leveraged new technologies and the growing scientific understanding of many rare diseases to develop groundbreaking therapies in recent years, including: