Dose Finding for Continuous and Ordinal Outcomes with a Monotone Objective Function: A Unified Approach
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Publication:93669
DOI10.1111/j.1541-0420.2008.01045.xzbMath1159.62334OpenAlexW1966316100WikidataQ42084799 ScholiaQ42084799MaRDI QIDQ93669
Se Hee Kim, Anastasia Ivanova, Sehee Kim, Anastasia Ivanova
Publication date: 13 May 2008
Published in: Biometrics (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1111/j.1541-0420.2008.01045.x
Related Items (8)
Evaluation of phase I clinical trial designs for combinational agents along with guidance based on simulation studies ⋮ Adaptive isotonic estimation of the minimum effective and peak doses in the presence of covariates ⋮ Continual reassessment method with multiple toxicity constraints ⋮ On the consistency of the continual reassessment method with multiple toxicity constraints ⋮ Risk-Group-Specific Dose Finding Based on an Average Toxicity Score ⋮ The treatment versus experimentation dilemma in dose finding studies ⋮ UnifiedDoseFinding ⋮ A study of the probit model with latent variables in Phase I clinical trials
Uses Software
Cites Work
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- Sequential search of an optimal dosage: Non‐bayesian methods
- Sequential Designs for Phase I Clinical Trials with Late‐Onset Toxicities
- The Continual Reassessment Method for Multiple Toxicity Grades: A Bayesian Quasi‐Likelihood Approach
- Dose-Finding Based on Multiple Toxicities in a Soft Tissue Sarcoma Trial
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