Drugs Against Rare Diseases: Are The Regulatory Standards Higher?
Clin Pharmacol Ther
; 100(4): 322-3, 2016 10.
Article
in En
| MEDLINE
| ID: mdl-27326701
The US Food and Drug Administration (FDA) recently issued a draft Guidance for Industry for Rare Diseases: Common Issues in Drug Development (referred to as "Rare Diseases Guidance"). In our opinion, the FDA should consider: (a) explicitly acknowledging the standards are higher for rare diseases for the reasons presented in this article; and (b) illustrating innovative development pathways that may be acceptable for rare diseases, including case studies.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Orphan Drug Production
/
United States Food and Drug Administration
/
Guidelines as Topic
/
Drug Approval
/
Rare Diseases
Type of study:
Guideline
Limits:
Humans
Country/Region as subject:
America do norte
Language:
En
Journal:
Clin Pharmacol Ther
Year:
2016
Document type:
Article
Affiliation country:
United States
Country of publication:
United States