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 临床试验研究设计终点和生物标志物药物安全性 890条(本栏目收费,不能显示细节,电话13136136841)
overview,251–252 251 252 
progression-free survival comparison,252 252 
DNA microarray colon cancer,343–344 343 344 
cytogenetics confluence in hematological cancers,323 323 
hepatocellular carcinoma,344–345 344 345 
interferon-α gene expression response,530–531 530 531 
ovarian cancer,342–343 342 343 
overview,341 341 
subgroup stratification,87–88 87 88 
Docetaxel Gradishar study,224–225 224 225 
Dose animal studies for estimation,13–15,18 13 15 18 
escalation and Moore schema,41–43 41 43 
ICH guidelines,18 18 
modification for adverse events,420–423 420 423 
units expressed in terms of body surface area,35–36 35 36 
Dose-limiting toxicity (DLT),18,42–43 18 42 43 
Double-blind study,112 112 
Double-dummy study,112 112 
Doxorubicin resistance,78 78 
toxicity,74,76 74 76 
Drug Amendments Act of 1962,580 580 
Drug origins animal models,11–15 11 15 
antibody drugs,7–9 7 9 
cladribine,5–6 5 6 
5-fluorouracil,3 3 
high-throughput screening,7 7 
methotrexate,3–4 3 4 
overview,1–2 1 2 
paclitaxel,4–5 4 5 
ribavirin,4 4 
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