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. 2012 May 15:205 Suppl 2:S250-7.
doi: 10.1093/infdis/jis041. Epub 2012 Mar 22.

Innovative trial designs are practical solutions for improving the treatment of tuberculosis

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Innovative trial designs are practical solutions for improving the treatment of tuberculosis

Patrick P J Phillips et al. J Infect Dis. .

Abstract

A growing number of new drugs for the treatment of tuberculosis are in clinical development. Confirmatory phase 3 trials are expensive and time-consuming and the question of whether one particular drug combination can be used to treat tuberculosis is less important from a public health perspective than the question of which are the shortest, simplest, most effective, and safest regimens. While preclinical and phase 1 studies provide some guidance in the selection of combinations for clinical evaluation, a large number of combinations will require phase 2 testing to ensure that only the best regimens advance to phase 3. The multi-arm multi-stage trial design is an example of a treatment selection-adaptive design where multiple experimental arms are each simultaneously compared with a common control and interim analyses allow for poor performing arms to be dropped early. Such designs, if designed and implemented correctly, require fewer patients, can be completed in a shorter time frame, and answer more relevant questions without any loss in statistical validity or scientific integrity. There are, however, practical issues that must be considered in applying this in tuberculosis treatment trials. More innovative trials designs should be considered to speed drug and regimen development for the treatment of tuberculosis.

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Comment in

  • Innovative trial designs to improving tuberculosis drug development.
    Dodd LE, Proschan MA. Dodd LE, et al. J Infect Dis. 2013 Feb 1;207(3):544. doi: 10.1093/infdis/jis704. Epub 2012 Nov 21. J Infect Dis. 2013. PMID: 23175767 Free PMC article. No abstract available.
  • Reply to Dodd and Proschan.
    Phillips PP, Bratton DJ, Nunn AJ, Hoelscher M. Phillips PP, et al. J Infect Dis. 2013 Feb 1;207(3):544-5. doi: 10.1093/infdis/jis705. Epub 2012 Nov 21. J Infect Dis. 2013. PMID: 23175768 No abstract available.

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