| Literature DB >> 29473145 |
Robert N Schuck1, Janet Woodcock2, Issam Zineh1, Peter Stein3, Jonathan Jarow2, Robert Temple2, Thomas Permutt4, Lisa LaVange4, Julia A Beaver3, Rosane Charlab1, Gideon M Blumenthal3, Sarah E Dorff1, Christopher Leptak3, Steven Lemery3, Hobart Rogers1, Badrul Chowdhury3, E David Litwack5, Michael Pacanowski1.
Abstract
Advances in our understanding of the molecular underpinnings of disease have spurred the development of targeted therapies and the use of precision medicine approaches in patient care. While targeted therapies have improved our capability to provide effective treatments to patients, they also present additional challenges to drug development and benefit-risk assessment such as identifying the subset(s) of patients likely to respond to the drug, assessing heterogeneity in response across molecular subsets of a disease, and developing diagnostic tests to identify patients for treatment. These challenges are particularly difficult to address when targeted therapies are developed to treat diseases with multiple molecular subtypes that occur at low frequencies. To help address these challenges, the US Food and Drug Administration recently published a draft guidance entitled "Developing Targeted Therapies in Low-Frequency Molecular Subsets of a Disease." Here we provide additional information on specific aspects of targeted therapy development in diseases with low-frequency molecular subsets. Published 2018. This article is a U.S. Government work and is in the public domain in the USA.Entities:
Mesh:
Year: 2018 PMID: 29473145 PMCID: PMC6347014 DOI: 10.1002/cpt.1041
Source DB: PubMed Journal: Clin Pharmacol Ther ISSN: 0009-9236 Impact factor: 6.875