A new pragmatic design for dose escalation in phase 1 clinical trials using an adaptive continual reassessment method
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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.
Nội dung trích xuất từ tài liệu:
A new pragmatic design for dose escalation in phase 1 clinical trials using an adaptive continual reassessment method
Nội dung trích xuất từ tài liệu:
A new pragmatic design for dose escalation in phase 1 clinical trials using an adaptive continual reassessment method
Tìm kiếm theo từ khóa liên quan:
BMC Cancer Adaptive design Bayesian adaptive Maximal tolerated dose Dose-finding Model-based design Rule-based designTài liệu có liên quan:
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