tailieunhanh - A new pragmatic design for dose escalation in phase 1 clinical trials using an adaptive continual reassessment method

A key challenge in phase I trials is maintaining rapid escalation in order to avoid exposing too many patients to sub-therapeutic doses, while preserving safety by limiting the frequency of toxic events. | A new pragmatic design for dose escalation in phase 1 clinical trials using an adaptive continual reassessment method

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