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Statistical Methods in Medical Research|June 8, 2019
Dose optimisation with simultaneous pharmacokinetic estimation in adaptive clinical trialsKabir Soeny, Barbara Bogacka, Byron JonesComputer Methods and Programs in Biomedicine|February 15, 2021
Model based dose personalization in clinical trialsKabir Soeny, Barbara Bogacka, Byron JonesJournal of Biopharmaceutical Statistics|May 27, 2015
Optimizing dose regimens and fixed dose combination ratios in clinical trialsKabir Soeny, Barbara Bogacka, Byron Jones, et al.Journal of Biopharmaceutical Statistics|December 14, 2004
Comparison of two design optimality criteria applied to a nonlinear modelBarbara Bogacka, Francis WrightJournal of Biopharmaceutical Statistics|July 10, 2024
A constrained optimum adaptive design for dose finding in early phase clinical trialsM Iftakhar Alam, Barbara Bogacka, D Stephen CoadStatistics in Medicine|June 28, 2019
Combined criteria for dose optimisation in early phase clinical trialsM Iftakhar Alam, D Stephen Coad, Barbara BogackaPolski Merkuriusz Lekarski : Organ Polskiego Towarzystwa Lekarskiego|December 27, 2016
[Pancreatic cancer microenvironment]Krzysztof Dąbkowski, Barbara Bogacka, Maciej Tarnowski, et al.Statistical Methods in Medical Research|June 23, 2005
The design of multicentre trialsValerii Fedorov, Byron JonesPharmaceutical Statistics|December 14, 2011
Viewpoint: observations on scaled average bioequivalenceScott D Patterson, Byron JonesPharmaceutical Statistics|May 4, 2007
A brief review of Phase 1 and Clinical Pharmacology statistics in clinical drug developmentScott D Patterson, Byron JonesPageof 4