Alternate approaches for pediatric type 1 diabetes drug development and potential regulatory approval: a perspective.
نویسندگان
چکیده
The incidence and prevalence of pediatric type 1 diabetes are increasing globally, including in the U.S. While the increasing number of cases of pediatric diabetes makes expeditious availability of new medical products and therapies for diabetes care essential, there have been many barriers encountered in bringing some drugs and devices to pediatric patients who may benefit. Newer insulins have been studied and approved for use in children. However, hurdles exist in the inclusion of children in studies of therapies aimed at preventing β-cell loss in those with new-onset diabetes and those at risk for type 1 diabetes. This Perspective focuses on potential solutions to the challenges experienced in bringing new drugs for pediatric type 1 diabetes to marketing approval. Given their central importance as the users of medical products, patient perspectives are included along with scientific and regulatory considerations.
منابع مشابه
Improving Pediatric Drug Development: Challenges, Opportunities and Lessons Learned
Pediatric drug development has been challenging for more than 5 decades. Two recent books; one a workshop report and the other a volume prepared from the perspective of the pharmaceutical industry offer modest hope that clinical therapeutics within this vulnerable population is beginning to be addressed. Both unfortunately focus predominantly on pediatric drug development within the US, however...
متن کاملAlternate-site testing is reliable in children and adolescents with type 1 diabetes, except at the forearm for hypoglycemia detection.
S elf-monitoring of blood glucose (SMBG) is crucial to the management of type 1 diabetes (1,2). Until recently, SMBG relied only on capillary blood sampling by fingerstick (a source of pain) and other forms of patient discomfort likely to diminish adherence to SMBG. After approval of alternate-site testing (AST), clinical studies found differences across measurement sites (3) in diabetic adults...
متن کاملResponse to Bell: industry perspective.
D avid S.H. Bell’s letter in the March issue of Diabetes Care (1) raises important and timely concerns about the ethics of conducting placebo controlled trials for regulatory approval of compounds for the treatment of type 2 diabetes. Standard pivotal trial design involves withdrawal of patients from current therapy and comparison of the investigational drug with an inactive placebo rather than...
متن کاملThe Food and Drug Administration and the Future of Drug Development for the Treatment of Diabetes.
The U.S. Food and Drug Administration (FDA) regulates the marketing of drugs in the United States. The FDA staff faces substantial challenges in evaluating preclinical and clinical trial data for a proposed new drug and deciding whether the resultant benefit-risk assessment supports marketing approval. Any approval decision will be associated with uncertainty regarding the drug's true risks and...
متن کاملDirect-acting antiviral drug approvals for treatment of chronic hepatitis C virus infection: Scientific and regulatory approaches to clinical trial designs.
Therapeutic options for treatment of chronic hepatitis C have improved substantially since the approval of direct-acting antiviral agents (DAAs). Several interferon (IFN)-free or IFN- and ribavirin (RBV)-free treatment regimens with shorter durations and improved efficacy and safety profiles are now available. The U.S. Food and Drug Administration (FDA) used several scientific approaches and re...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Diabetes care
دوره 38 10 شماره
صفحات -
تاریخ انتشار 2015