Literature DB >> 19384686

Optimal cost-effective designs of Phase II proof of concept trials and associated go-no go decisions.

Cong Chen1, Robert A Beckman.   

Abstract

This manuscript discusses optimal cost-effective designs for Phase II proof of concept (PoC) trials. Unlike a confirmatory registration trial, a PoC trial is exploratory in nature, and sponsors of such trials have the liberty to choose the type I error rate and the power. The decision is largely driven by the perceived probability of having a truly active treatment per patient exposure (a surrogate measure to development cost), which is naturally captured in an efficiency score to be defined in this manuscript. Optimization of the score function leads to type I error rate and power (and therefore sample size) for the trial that is most cost-effective. This in turn leads to cost-effective go-no go criteria for development decisions. The idea is applied to derive optimal trial-level, program-level, and franchise-level design strategies. The study is not meant to provide any general conclusion because the settings used are largely simplified for illustrative purposes. However, through the examples provided herein, a reader should be able to gain useful insight into these design problems and apply them to the design of their own PoC trials.

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Year:  2009        PMID: 19384686     DOI: 10.1080/10543400902800478

Source DB:  PubMed          Journal:  J Biopharm Stat        ISSN: 1054-3406            Impact factor:   1.051


  8 in total

Review 1.  Integrating predictive biomarkers and classifiers into oncology clinical development programmes.

Authors:  Robert A Beckman; Jason Clark; Cong Chen
Journal:  Nat Rev Drug Discov       Date:  2011-09-30       Impact factor: 84.694

Review 2.  Innovations in Clinical Development in Rare Diseases of Children and Adults: Small Populations and/or Small Patients.

Authors:  Robert A Beckman; Zoran Antonijevic; Mercedeh Ghadessi; Heng Xu; Cong Chen; Yi Liu; Rui Tang
Journal:  Paediatr Drugs       Date:  2022-10-15       Impact factor: 3.930

3.  Current issues in oncology drug development, with a focus on Phase II trials.

Authors:  Daniel J Sargent; Jeremy M G Taylor
Journal:  J Biopharm Stat       Date:  2009       Impact factor: 1.051

Review 4.  Decision-theoretic designs for small trials and pilot studies: A review.

Authors:  Siew Wan Hee; Thomas Hamborg; Simon Day; Jason Madan; Frank Miller; Martin Posch; Sarah Zohar; Nigel Stallard
Journal:  Stat Methods Med Res       Date:  2015-06-05       Impact factor: 3.021

5.  PIPELINEs: Creating Comparable Clinical Knowledge Efficiently by Linking Trial Platforms.

Authors:  M R Trusheim; A A Shrier; Z Antonijevic; R A Beckman; R K Campbell; C Chen; K T Flaherty; J Loewy; D Lacombe; S Madhavan; H P Selker; L J Esserman
Journal:  Clin Pharmacol Ther       Date:  2016-10-19       Impact factor: 6.875

6.  Decision-theoretic designs for a series of trials with correlated treatment effects using the Sarmanov multivariate beta-binomial distribution.

Authors:  Siew Wan Hee; Nicholas Parsons; Nigel Stallard
Journal:  Biom J       Date:  2017-07-26       Impact factor: 2.207

7.  A digital intervention targeting cognitive control network dysfunction in middle age and older adults with major depression.

Authors:  Faith M Gunning; Joaquin A Anguera; Lindsay W Victoria; Patricia A Areán
Journal:  Transl Psychiatry       Date:  2021-05-04       Impact factor: 6.222

8.  New evidence-based adaptive clinical trial methods for optimally integrating predictive biomarkers into oncology clinical development programs.

Authors:  Robert A Beckman; Cong Chen
Journal:  Chin J Cancer       Date:  2013-03-15
  8 in total

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