A Comparison of Treatment Effect Sizes in Matched Phase 2 and Phase 3 Trials of Advanced Therapeutics in Inflammatory Bowel Disease: Systematic Review and Meta-Analysis

Author:

Hanzel Jurij12,Solitano Virginia34,Zou Lily5,Zou G.Y.267,Peyrin-Biroulet Laurent8,Danese Silvio9,Singh Siddharth10,Ma Christopher21112,Wils Pauline1314,Jairath Vipul236

Affiliation:

1. Department of Gastroenterology and Hepatology, University Medical Center Ljubljana, Ljubljana, Slovenia;

2. Alimentiv Inc, London, Ontario, Canada;

3. Division of Gastroenterology, Department of Medicine, Western University, London, Ontario, Canada;

4. Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy;

5. Department of Statistics and Actuarial Sciences, University of Waterloo, Waterloo, Ontario, Canada;

6. Department of Epidemiology and Biostatistics, Western University, London, Ontario, Canada;

7. Robarts Research Institute, Western University, London, Ontario, Canada;

8. Department of Gastroenterology and Inserm NGERE U1256, University Hospital of Nancy, University of Lorraine, Nancy, France;

9. Gastroenterology and Endoscopy, IRCCS Ospedale San Raffaele and University Vita‐Salute San Raffaele, Milan, Italy;

10. Division of Gastroenterology, University of California, San Diego, La Jolla, California, USA;

11. Division of Gastroenterology & Hepatology, Department of Medicine, University of Calgary, Calgary, Alberta, Canada;

12. Department of Community Health Sciences, University of Calgary, Calgary, Alberta, Canada;

13. Department of Gastroenterology, Claude Huriez Hospital, University of Lille 2, Lille, France;

14. Inserm, CHU Lille, U1286 Infinite, Institute for Translational Research in Inflammation, University of Lille, Lille, France.

Abstract

INTRODUCTION: Phase 2 trials are fundamental to the rational and efficient design of phase 3 trials. We aimed to determine the relationship of treatment effect size estimates from phase 2 and phase 3 clinical trials on advanced therapeutics in inflammatory bowel disease. METHODS: MEDLINE, EMBASE, CENTRAL, and the Cochrane library were searched from inception to December 19, 2022, to identify paired phase 2 and 3 placebo-controlled induction studies of advanced therapeutics for Crohn's disease (CD) and ulcerative colitis (UC). Treatment effect sizes were expressed as a risk ratio (RR) between the active arm and placebo arm. For the same therapeutics, RRs from phase 2 trials were divided by the RR from phase 3 trial to quantify the relationship of effect sizes between phases. RESULTS: Twenty-two studies (9 phase 2 trials, 13 phase 3 trials) were included for CD and 30 studies (12 phase 2 trials, 18 phase 3 trials) for UC. In UC (pooled RR 0.72; 95% confidence interval: 0.58–0.86; RR <1 indicates smaller treatment effect sizes in phase 2 trials), but not CD (pooled RR 1.01; 95% confidence interval: 0.84–1.18), phase 2 trials systematically underestimated treatment effect sizes for the primary endpoint compared with phase 3 trials. The underestimation was observed for clinical, but not endoscopic, endpoints in UC. DISCUSSION: Treatment effect sizes for the primary and clinical endpoints were similar across clinical trial phases in CD, but not UC, where only endoscopic endpoints were comparable. This will help inform clinical development plans and future trial design.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology

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