TY - JOUR
T1 - Prevention and interception trials in inflammatory bowel disease
T2 - an international taskforce assessment on clinical trial design
AU - Honap, Sailish
AU - Agrinier, Nelly
AU - Torres, Joana
AU - Croitoru, Kenneth
AU - Lee, Sun Ho
AU - Turpin, Williams
AU - Ungaro, Ryan C.
AU - Agrawal, Manasi
AU - Peter, Inga
AU - Turner, Dan
AU - Dotan, Iris
AU - Hart, Ailsa L.
AU - Netter, Patrick
AU - D'Haens, Geert
AU - Rubin, David T.
AU - Ng, Siew C.
AU - Gearry, Richard
AU - Jairath, Vipul
AU - Ananthakrishnan, Ashwin N.
AU - Danese, Silvio
AU - Colombel, Jean Frederic
AU - Peyrin-Biroulet, Laurent
N1 - Publisher Copyright:
© 2025 Elsevier Ltd
PY - 2025
Y1 - 2025
N2 - Therapeutic progress in inflammatory bowel disease (IBD) has hitherto focused on reducing inflammation to minimise long-term complications. However, strategies aimed at preventing IBD and attenuating its disease course are particularly appealing. This concept is derived from accumulating evidence for an “at-risk” preclinical state and the associations linking genetic background and numerous environmental exposures to disease pathogenesis. Trials in rheumatoid arthritis and type 1 diabetes have identified interventions to delay disease onset, modify the subsequent disease course (potentially protecting against irreversible tissue and end organ damage), and prolong normal quality of life. Prevention and interception trials have major challenges compared with therapeutic trials across a number of domains, including ethical considerations, eligibility criteria, sample size, and optimal endpoints. This Review investigates important factors in designing high-quality prevention trials and evaluates the feasibility and current progress of such trials in IBD, aiming to identify therapeutic strategies for populations at risk.
AB - Therapeutic progress in inflammatory bowel disease (IBD) has hitherto focused on reducing inflammation to minimise long-term complications. However, strategies aimed at preventing IBD and attenuating its disease course are particularly appealing. This concept is derived from accumulating evidence for an “at-risk” preclinical state and the associations linking genetic background and numerous environmental exposures to disease pathogenesis. Trials in rheumatoid arthritis and type 1 diabetes have identified interventions to delay disease onset, modify the subsequent disease course (potentially protecting against irreversible tissue and end organ damage), and prolong normal quality of life. Prevention and interception trials have major challenges compared with therapeutic trials across a number of domains, including ethical considerations, eligibility criteria, sample size, and optimal endpoints. This Review investigates important factors in designing high-quality prevention trials and evaluates the feasibility and current progress of such trials in IBD, aiming to identify therapeutic strategies for populations at risk.
UR - http://www.scopus.com/inward/record.url?scp=105001696521&partnerID=8YFLogxK
U2 - 10.1016/s2468-1253(24)00439-4
DO - 10.1016/s2468-1253(24)00439-4
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C2 - 40187359
AN - SCOPUS:105001696521
SN - 2468-1253
JO - The Lancet Gastroenterology and Hepatology
JF - The Lancet Gastroenterology and Hepatology
ER -