Lisa V Hampson

Designing and evaluating dose-escalation studies made easy: The MoDEsT web app

Philip Pallmann, Fang Wan, Adrian P Mander, 2019, Clinical trials.

Optimizing the data combination rule for seamless phase II/III clinical trials

Lisa V Hampson, Christopher Jennison, Lisa V. Hampson, 2014, Statistics in medicine.

Designing multi‐arm multi‐stage clinical trials using a risk–benefit criterion for treatment selection

Lisa V Hampson, Thomas Jaki, Lisa V. Hampson, 2015, Statistics in medicine.

DELTA2 guidance on choosing the target difference and undertaking and reporting the sample size calculation for a randomised controlled trial

David Armstrong, Lisa V Hampson, Nigel Stallard, 2018, British Medical Journal.

A robust Bayesian meta-analytic approach to incorporate animal data into phase I oncology trials

Lisa V Hampson, Simon Wandel, Lisa V. Hampson, 2020, Statistical methods in medical research.

A framework for prospectively defining progression rules for internal pilot studies monitoring recruitment

Lisa V Hampson, Thomas Jaki, Paula R Williamson, 2018, Statistical methods in medical research.

Extrapolation of efficacy and other data to support the development of new medicines for children: A systematic review of methods

Lisa V Hampson, Thomas Jaki, Lisa V. Hampson, 2018, Statistical methods in medical research.

Bayesian methods for the design and interpretation of clinical trials in very rare diseases

Lisa V Hampson, John Whitehead, Lisa V. Hampson, 2014, Statistics in medicine.