Process / pipelineClinical trial design

Dose-Escalation Design (Continual Reassessment Method)

Dose-Escalation Design, formalized as the Continual Reassessment Method (CRM), is a Bayesian adaptive algorithm for identifying the Maximum Tolerated Dose (MTD) in Phase I clinical trials. Introduced by John O'Quigley, Margaret Pepe, and Lloyd Fisher in 1990, CRM treats dose-toxicity response as a parametric curve, updates a prior probability model after each patient's outcome, and assigns subsequent patients to the dose currently estimated closest to a pre-specified target toxicity probability.

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Sources

  1. O'Quigley, J., Pepe, M., & Fisher, L. (1990). Continual reassessment method: a practical design for phase 1 clinical trials in cancer. Biometrics, 46(1), 33–48. DOI: 10.2307/2531628

Related methods

ScholarGateDose-Escalation Design (Dose-Escalation Design (Continual Reassessment Method)). Retrieved 2026-06-04 from https://scholargate.app/tr/experimental-design/dose-escalation-design