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Modified Toxicity Probability Interval Design: A Safer and More Reliable Method Than the 3 + 3 Design for Practical Phase I Trials

The 3 + 3 design is the most common choice among clinicians for phase I dose-escalation oncology trials. In recent reviews, more than 95% of phase I trials have been based on the 3 + 3 design. Given that it is intuitive and its implementation does not require a computer program, clinicians can condu...

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Autors principals: Ji, Yuan, Wang, Sue-Jane
Format: Artigo
Idioma:Inglês
Publicat: American Society of Clinical Oncology 2013
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3641699/
https://ncbi.nlm.nih.gov/pubmed/23569307
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1200/JCO.2012.45.7903
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