Drug-resistant tuberculosis treatments, the case for a phase III platform trial
Most phase III trials in drug-resistant tuberculosis have either been underpowered to quantify differences in microbiological endpoints or have taken up to a decade to complete. Composite primary endpoints, dominated by differences in treatment discontinuation and regimen changes, may mask important...
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Veröffentlicht in: | Bulletin of the World Health Organization 2024-09, Vol.102 (9), p.657-664 |
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creator | Yates, Tom A Barnes, Samara Dedicoat, Martin Kon, Onn Min Kunst, Heinke Lipman, Marc Millington, Kerry A Nunn, Andrew J Phillips, Patrick Pj Potter, Jessica L Squire, S Bertel |
description | Most phase III trials in drug-resistant tuberculosis have either been underpowered to quantify differences in microbiological endpoints or have taken up to a decade to complete. Composite primary endpoints, dominated by differences in treatment discontinuation and regimen changes, may mask important differences in treatment failure and relapse. Although new regimens for drug-resistant tuberculosis appear very effective, resistance to new drugs is emerging rapidly. There is a need for shorter, safer and more tolerable regimens, including those active against bedaquiline-resistant tuberculosis. Transitioning from multiple regimen A versus regimen B trials to a single large phase III platform trial would accelerate the acquisition of robust estimates of relative efficacy and safety. Further efficiencies could be achieved by adopting modern adaptive platform designs. Collaboration among trialists, affected community representatives, funders and regulators is essential for developing such a phase III platform trial for drug-resistant tuberculosis treatment regimens. |
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Composite primary endpoints, dominated by differences in treatment discontinuation and regimen changes, may mask important differences in treatment failure and relapse. Although new regimens for drug-resistant tuberculosis appear very effective, resistance to new drugs is emerging rapidly. There is a need for shorter, safer and more tolerable regimens, including those active against bedaquiline-resistant tuberculosis. Transitioning from multiple regimen A versus regimen B trials to a single large phase III platform trial would accelerate the acquisition of robust estimates of relative efficacy and safety. Further efficiencies could be achieved by adopting modern adaptive platform designs. 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Composite primary endpoints, dominated by differences in treatment discontinuation and regimen changes, may mask important differences in treatment failure and relapse. Although new regimens for drug-resistant tuberculosis appear very effective, resistance to new drugs is emerging rapidly. There is a need for shorter, safer and more tolerable regimens, including those active against bedaquiline-resistant tuberculosis. Transitioning from multiple regimen A versus regimen B trials to a single large phase III platform trial would accelerate the acquisition of robust estimates of relative efficacy and safety. Further efficiencies could be achieved by adopting modern adaptive platform designs. 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Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yates, Tom A</au><au>Barnes, Samara</au><au>Dedicoat, Martin</au><au>Kon, Onn Min</au><au>Kunst, Heinke</au><au>Lipman, Marc</au><au>Millington, Kerry A</au><au>Nunn, Andrew J</au><au>Phillips, Patrick Pj</au><au>Potter, Jessica L</au><au>Squire, S Bertel</au><aucorp>UK Academics and Professionals to end TB</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Drug-resistant tuberculosis treatments, the case for a phase III platform trial</atitle><jtitle>Bulletin of the World Health Organization</jtitle><addtitle>Bull World Health Organ</addtitle><date>2024-09-01</date><risdate>2024</risdate><volume>102</volume><issue>9</issue><spage>657</spage><epage>664</epage><pages>657-664</pages><issn>0042-9686</issn><issn>1564-0604</issn><eissn>1564-0604</eissn><abstract>Most phase III trials in drug-resistant tuberculosis have either been underpowered to quantify differences in microbiological endpoints or have taken up to a decade to complete. Composite primary endpoints, dominated by differences in treatment discontinuation and regimen changes, may mask important differences in treatment failure and relapse. Although new regimens for drug-resistant tuberculosis appear very effective, resistance to new drugs is emerging rapidly. There is a need for shorter, safer and more tolerable regimens, including those active against bedaquiline-resistant tuberculosis. Transitioning from multiple regimen A versus regimen B trials to a single large phase III platform trial would accelerate the acquisition of robust estimates of relative efficacy and safety. Further efficiencies could be achieved by adopting modern adaptive platform designs. 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subjects | Adaptive Clinical Trials as Topic Antitubercular Agents - therapeutic use Clinical trials Clinical Trials, Phase III as Topic Collaboration Cooperation Courts Diarylquinolines - therapeutic use Discontinued Drug abuse Drug development Drug resistance Drugs Effectiveness Efficacy Estimates Humans Multidrug resistant organisms Policy & Practice Relapse Standard of care Trials Tuberculosis Tuberculosis, Multidrug-Resistant - drug therapy |
title | Drug-resistant tuberculosis treatments, the case for a phase III platform trial |
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