Adaptive trial designs in rheumatology: Report from the OMERACT special interest group

Tim Pickles, Rieke Alten, Maarten Boers, Vivian Bykerk, Jared Christensen, Robin Christensen, Hubert van Hoogstraten, Lee S. Simon, Lai-Shan Tam, Ernest H. Choy

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Objective. Adaptive trial design was developed initially for oncology to improve trial efficiency. If optimized for rheumatology, it may improve trial efficiency by reducing sample size and time. Methods. A systematic review assessed design of phase II clinical trials in rheumatoid arthritis. Results. Fifty-six trials were reviewed. Most trials had 4 groups (1 control and 3 intervention), with an average group size of 34 patients. American College of Rheumatology 20 measured at 16 weeks was the most commonly used primary endpoint. Conclusion. The next step is to undertake a systematic review of adaptive designs used in early-phase
Original languageEnglish
Pages (from-to)1406-1408
Number of pages3
JournalJournal of Rheumatology
Volume46
Issue number10
DOIs
Publication statusPublished - Oct 2019

Cite this

Pickles, T., Alten, R., Boers, M., Bykerk, V., Christensen, J., Christensen, R., ... Choy, E. H. (2019). Adaptive trial designs in rheumatology: Report from the OMERACT special interest group. Journal of Rheumatology, 46(10), 1406-1408. https://doi.org/10.3899/jrheum.181054