医学
冲刷
临床试验
重症监护医学
德尔菲法
随机对照试验
随机化
炎症性肠病
德尔菲
临床实习
梅德林
临床决策
Golimumab公司
克罗恩病
疾病
作者
P Wils,Vipul Jairath,Bruce E Sands,Axel Dignass,Fernando Magro,David T Rubin,Iris Dotan,Walter Reinisch,Parambir Dulai,Richard Gearry,Christopher Ma,Millie Long,Alessandro Armuzzi,Taku Kobayashi,D Turner,Sophie Vieujean,Bram Verstockt,Ailsa Hart,Silvio Danese,Laurent Peyrin-Biroulet
标识
DOI:10.1093/ecco-jcc/jjag060
摘要
BACKGROUND & AIMS: Prolonged washout periods between advanced therapies and investigational drugs are commonly required in inflammatory bowel disease (IBD) randomized controlled trials (RCTs). These requirements restrict patient enrollment and diverge from real-world clinical practice. This study aimed to establish an international expert consensus on washout durations for advanced therapies and conventional immunosuppressants (IS) in IBD clinical trials and to propose methodological recommendations for future study designs. METHODS: An international panel of 12 IBD clinical trial experts participated in a Delphi consensus process. Agreement of ≥75% among participants was predefined as consensus. RESULTS: A total of 12 statements were approved. Consensus was reached to eliminate washout periods for conventional IS (thiopurines, tacrolimus, methotrexate, and mycophenolate mofetil). For golimumab and ozanimod, experts agreed on a 2-week washout period. For other biologics (infliximab, adalimumab, vedolizumab, ustekinumab, and anti-IL-23 agents), most participants favored a 2-4-week washout duration and for JAK inhibitors and etrasimod, participants supported a short 2-week washout, though without reaching formal consensus. Experts recommended incorporating washout-based stratification (<4 vs ≥4 weeks) at randomization into future trial designs to evaluate its impact on safety, pharmacokinetics, and efficacy outcomes. CONCLUSIONS: This international Delphi consensus highlights the need to adapt current washout practices in IBD RCTs to real-world practice. Experts supported shorter and standardized washout durations-preferably less than 4 weeks-to better align with clinical practice, while maintaining patient safety. Acceptance of these recommendations by regulators could harmonize washout duration criteria, enhance recruitment efficiency, and accelerate patient access to innovative therapies without compromising safety.
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