| Literature DB >> 33258093 |
Sarah Sheehan1,2, Gerri Baer3, Morgan Romine4, Lynn Hudson5, Robert Lim3, Elektra Papadopoulos3, Michelle Campbell3, Gregory Daniel4, Susan McCune3.
Abstract
Chronic pulmonary and respiratory conditions associated with preterm birth are incompletely characterized, complicating long-term treatment and development of more effective therapies. Stakeholders face challenges in the development of validated, clinically meaningful endpoints that adequately measure morbidities and predict or represent health outcomes for preterm neonates. We propose in this paper a research agenda, informed by the input of experts from a 2018 workshop we convened on this topic, to advance endpoint and treatment development. We discuss the necessity of further evaluation of existing endpoints and the improved characterization of disease endotypes. We also discuss key steps to the development of optimized short- and long-term endpoints that can be linked to meaningful health outcomes. Finally, we discuss the importance of limiting variability in data collection and the application of new clinical trial endpoints as well as the critical nature of multi-stakeholder collaboration to advancing therapeutic development for this vulnerable patient population.Entities:
Keywords: Bronchopulmonary dysplasia; Chronic pulmonary insufficiency of prematurity; Endpoint development; Preterm; Pulmonary outcomes
Mesh:
Year: 2020 PMID: 33258093 PMCID: PMC9351457 DOI: 10.1007/s43441-020-00153-z
Source DB: PubMed Journal: Ther Innov Regul Sci ISSN: 2168-4790 Impact factor: 1.337