Dose-Finding Designs for HIV Studies
From MaRDI portal
Publication:3078854
DOI10.1111/j.0006-341X.2001.01018.xzbMath1209.62319OpenAlexW2032289930WikidataQ77412020 ScholiaQ77412020MaRDI QIDQ3078854
Michael D. Hughes, John O'Quigley, Terry Fenton
Publication date: 1 March 2011
Published in: Biometrics (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1111/j.0006-341x.2001.01018.x
dose-finding studiescontinual reassessment methodtoxicityphase I trialphase II trialdose escalationefficacy studiesHIV clinical trials
Applications of statistics to biology and medical sciences; meta analysis (62P10) Medical applications (general) (92C50)
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Cites Work
- Unnamed Item
- Continual Reassessment Method: A Practical Design for Phase 1 Clinical Trials in Cancer
- Using a one-parameter model to sequentially estimate the root of a regression function.
- Consistency of continual reassessment method under model misspecification
- Miscellanea. A stopping rule for the continual reassessment method
- Continual Reassessment Method: A Likelihood Approach
- Estimating the Probability of Toxicity at the Recommended Dose Following a Phase I Clinical Trial in Cancer