APPTT
CLIN
Don Sanders, MD
Pediatrics
Riley Hospital for Children at Indiana University Health
Jennifer Guimbellot, MD, PhD
Pediatrics
Arkansas Children's Hospital/Arkansas Children's Research Institute
In the era of highly effective modulator therapy, the CF community continues to need biomarkers and outcome measures to accurately guide personalized treatments and improve long-term outcomes, as well as further develop new therapies for those who are ineligible or poorly responsive to currently available therapies. Attendees at this session will learn about novel research on known measures, such as sweat chloride and spirometry, as well as new predictive tools, monitoring strategies, and innovative approaches to measuring disease severity and response to interventions. This session consists of two main parts: poster viewing followed by a moderated discussion. It is designed to engage the authors and the audience in a discussion that ties together ideas from multiple posters in the session.
Speaker: William T. Harris, Birmingham, AL – UAB
Speaker: Katie Larson Ode, MD – University of Iowa
Speaker: Sivagurunathan Sutharsan, MD – Department of Pulmonary Medicine, Division of Cystic Fibrosis, University Medicine Essen -Ruhrlandklinik, University of Duisburg-Essen, Essen, Germany.
Speaker: Emilio Arteaga-Solis, MD, PhD – Vertex Pharmaceutical
Speaker: Angela Metcalf, MD – University of Colorado School of Medicine
Speaker: Josephine Ackah-Cudjoe, MSc – University of British Columbia
Speaker: Daniela F. Gutierrez-Munoz – Arizona State University
Speaker: Lisa Strug, ScM, PhD – The Hospital for Sick Children