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A hybrid phase I-II/III clinical trial design allowing dose re-optimization in phase III
Andrew G. Chapple,
Peter F. Thall
Biostatistics
Research output
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Contribution to journal
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Article
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peer-review
9
Scopus citations
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Dive into the research topics of 'A hybrid phase I-II/III clinical trial design allowing dose re-optimization in phase III'. Together they form a unique fingerprint.
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Mathematics
Reoptimization
100%
Dose
70%
Clinical Trials
61%
Design
39%
Survival Time
20%
Toxicity
13%
Efficacy
7%
Paradigm
7%
Evaluation
5%
Progression
4%
Randomisation
3%
Mixture Model
3%
Optimise
3%
Drugs
3%
Maximise
3%
Evaluate
2%
Simulation Study
2%
Agriculture & Biology
clinical trials
68%
dosage
33%
toxicity
16%
new drugs
9%
Medicine & Life Sciences
Clinical Trials
42%
Survival
26%
Random Allocation
15%
Progression-Free Survival
14%
Survival Rate
12%
Pharmaceutical Preparations
6%
Therapeutics
2%
Chemistry
Dose
49%
Maximum Tolerated Dose
36%
Time
19%
Drug
5%
Mixture
4%
Engineering & Materials Science
Toxicity
56%
Defects
10%