| Literature DB >> 34953790 |
Marc E Rothenberg1, Shawna K B Hottinger2, Nirmala Gonsalves3, Glenn T Furuta4, Margaret H Collins5, Nicholas J Talley6, Kathryn Peterson7, Calies Menard-Katcher4, Macie Smith8, Ikuo Hirano3, Robert M Genta9, Mirna Chehade10, Sandeep K Gupta11, Jonathan M Spergel12, Seema S Aceves13, Evan S Dellon14.
Abstract
The US Food and Drug Administration hosted a workshop on July 21, 2021, to discuss the disease characteristics, natural history, and end points to assess treatment benefit in patients with eosinophilic gastrointestinal disorders (EGIDs) beyond eosinophilic esophagitis (EoE). Notably, EGIDs beyond EoE, such as eosinophilic gastritis, eosinophilic enteritis, and eosinophilic colitis, herein referred to as non-EoE EGIDs, are understudied relative to EoE. This workshop provided a forum for open discussion among stakeholders-medical professionals (including their societies and research groups), Food and Drug Administration representatives, an industry representative, and a patient representative-to facilitate drug development. Experts in many disciplines related to EGIDs, including allergy, immunology, epidemiology, gastroenterology, and pathology, and both adult and pediatric clinicians contributed. Herein, we discuss some of the insights of the material presented at the meeting and present perspectives on moving the field forward toward drug approval.Entities:
Keywords: Consortium of Eosinophilic Gastrointestinal Disease Researchers (CEGIR); Food and Drug Administration (FDA); diagnosis; eosinophilic colitis; eosinophilic duodenitis; eosinophilic enteritis; eosinophilic gastritis; eosinophilic gastroenteritis; eosinophilic gastrointestinal disorder; food allergy; treatment
Mesh:
Year: 2021 PMID: 34953790 PMCID: PMC8901475 DOI: 10.1016/j.jaci.2021.12.768
Source DB: PubMed Journal: J Allergy Clin Immunol ISSN: 0091-6749 Impact factor: 10.793