Doussau, Adélaïde <br/><br/>
Dose-finding design using mixed-effect proportional odds model for longitudinal graded toxicity data in phase I oncology clinical trials.  [electronic resource] 

 -  Statistics in medicine  Dec 2013 
 - 5430-47 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1097-0258 
<br/><br/><label>Standard No.: </label>10.1002/sim.5960  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Antineoplastic Agents--administration & dosage<br/>Clinical Trials, Phase I as Topic--methods<br/>Computer Simulation<br/>Humans<br/>Likelihood Functions<br/>Longitudinal Studies<br/>Maximum Tolerated Dose<br/>Models, Statistical<br/>Neoplasms--drug therapy<br/>Plant Preparations--administration & dosage<br/>Ribosome Inactivating Proteins, Type 2--administration & dosage<br/>Toxins, Biological--administration & dosage