Catálogo bibliográfico FCT/UNL
Image from Google Jackets

Biopharmaceutical applied statistics symposium [Documento electrónico] = pharmaceutical applications / edited by Karl E. Peace, Ding-Geng Chen, Sandeep Menon, Volume 3

Secondary Author: Peace, Karl E., ed. lit.;Chen, Ding-Geng, ed. lit.;Menon, Sandeep, ed. lit.Language: eng.Country: US - United States of America.Publication: Singapore : Springer Singapore, Springer, 2018Description: XV, 426 p. : il.ISBN: 978-981-10-7820-0.Series: ICSA Book Series in StatisticsSubject - Topical Name: Estatística | Métodos estatísticos Online Resources:Click here to access online
Tags from this library: No tags from this library for this title. Log in to add tags.
Star ratings
    Average rating: 0.0 (0 votes)
Holdings
Item type Current library Collection Call number Copy number Status Date due Barcode
E-Books Biblioteca NOVA FCT Online Não Ficção QA276. FCT 98055 (Browse shelf(Opens below)) 1 Available

Colocação: Online

This BASS book Series publishes selected high-quality papers reflecting recent advances in the design and biostatistical analysis of biopharmaceutical experiments – particularly biopharmaceutical clinical trials.  The papers were selected from invited presentations at the Biopharmaceutical Applied Statistics Symposium (BASS), which was founded by the first Editor in 1994 and has since become the premier international conference in biopharmaceutical statistics. The primary aims of the BASS are: 1) to raise funding to support graduate students in biostatistics programs, and 2) to provide an opportunity for professionals engaged in pharmaceutical drug research and development to share insights into solving the problems they encounter. The BASS book series is initially divided into three volumes addressing: 1) Design of Clinical Trials; 2) Biostatistical Analysis of Clinical Trials; and 3) Pharmaceutical Applications.   This book is the third of the 3-volume book series. The topics covered include: Targeted Learning of Optimal Individualized Treatment Rules under Cost Constraints, Uses of Mixture Normal Distribution in Genomics and Otherwise, Personalized Medicine – Design Considerations, Adaptive Biomarker Subpopulation and Tumor Type Selection in Phase III Oncology Trials, High Dimensional Data in Genomics; Synergy or Additivity - The Importance of Defining the Primary Endpoint, Full Bayesian Adaptive Dose Finding Using Toxicity Probability Interval (TPI), Alpha-recycling for the Analyses of Primary and Secondary Endpoints of Clinical Trials, Expanded Interpretations of Results of Carcinogenicity Studies of Pharmaceuticals, Randomized Clinical Trials for Orphan Drug Development,  Mediation Modeling in Randomized Trials with Non-normal Outcome Variables, Statistical Considerations in Using Images in Clinical Trials, Interesting Applications over 30 Years of Consulting, Uncovering Fraud, Misconduct and Other Data Quality Issues in Clinical Trials, Development and Evaluation of High Dimensional Prognostic Models, and Design and Analysis of Biosimilar Studies.

There are no comments on this title.

to post a comment.
Moodle da Biblioteca Slideshare da Biblioteca Siga-nos no Issuu Twitter da Biblioteca Instagram da Biblioteca Facebook da Biblioteca Blog da Biblioteca