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Practical guidance for running late-phase platform protocols for clinical trials: lessons from experienced UK clinical trials units.
Love, Sharon B; Cafferty, Fay; Snowdon, Claire; Carty, Karen; Savage, Joshua; Pallmann, Philip; McParland, Lucy; Brown, Louise; Masters, Lindsey; Schiavone, Francesca; Hague, Dominic; Townsend, Stephen; Amos, Claire; South, Annabelle; Sturgeon, Kate; Langley, Ruth; Maughan, Timothy; James, Nicholas; Hall, Emma; Kernaghan, Sarah; Bliss, Judith; Turner, Nick; Tutt, Andrew; Yap, Christina; Firth, Charlotte; Kong, Anthony; Mehanna, Hisham; Watts, Colin; Hills, Robert; Thomas, Ian; Copland, Mhairi; Bell, Sue; Sebag-Montefiore, David; Jones, Robert; Parmar, Mahesh K B; Sydes, Matthew R.
Affiliation
  • Love SB; MRC Clinical Trials Unit at UCL, 90 High Holborn, London, WC1V 6LJ, UK. s.love@ucl.ac.uk.
  • Cafferty F; The Institute of Cancer Research, London, SW7 3RP, UK.
  • Snowdon C; The Institute of Cancer Research, London, SW7 3RP, UK.
  • Carty K; Cancer Research UK Clinical Trials Unit, Level 0 The Beatson West of Scotland Cancer Centre, 1053 Great Western Road, Glasgow, G12 0YN, UK.
  • Savage J; Cancer Research UK Clinical Trials Unit (CRCTU), Institute of Cancer and Genomic Sciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
  • Pallmann P; Centre for Trials Research, Cardiff University, Neuadd Meirionnydd, Heath Park, Cardiff, CF14 4YS, UK.
  • McParland L; PHASTAR, Bollo Lane, London, W4 5LE, UK.
  • Brown L; MRC Clinical Trials Unit at UCL, 90 High Holborn, London, WC1V 6LJ, UK.
  • Masters L; MRC Clinical Trials Unit at UCL, 90 High Holborn, London, WC1V 6LJ, UK.
  • Schiavone F; MRC Clinical Trials Unit at UCL, 90 High Holborn, London, WC1V 6LJ, UK.
  • Hague D; MRC Clinical Trials Unit at UCL, 90 High Holborn, London, WC1V 6LJ, UK.
  • Townsend S; MRC Clinical Trials Unit at UCL, 90 High Holborn, London, WC1V 6LJ, UK.
  • Amos C; MRC Clinical Trials Unit at UCL, 90 High Holborn, London, WC1V 6LJ, UK.
  • South A; MRC Clinical Trials Unit at UCL, 90 High Holborn, London, WC1V 6LJ, UK.
  • Sturgeon K; MRC Clinical Trials Unit at UCL, 90 High Holborn, London, WC1V 6LJ, UK.
  • Langley R; MRC Clinical Trials Unit at UCL, 90 High Holborn, London, WC1V 6LJ, UK.
  • Maughan T; University of Oxford, Oxford, OX3 7DQ, UK.
  • James N; The Institute of Cancer Research, London, SW7 3RP, UK.
  • Hall E; The Institute of Cancer Research, London, SW7 3RP, UK.
  • Kernaghan S; The Institute of Cancer Research, London, SW7 3RP, UK.
  • Bliss J; The Institute of Cancer Research, London, SW7 3RP, UK.
  • Turner N; The Institute of Cancer Research, London, SW7 3RP, UK.
  • Tutt A; The Institute of Cancer Research, London, SW3 6JB, UK.
  • Yap C; The Institute of Cancer Research, London, SW7 3RP, UK.
  • Firth C; Cancer Research UK Clinical Trials Unit, Institute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, B15 2TT, UK.
  • Kong A; Cancer Research UK Clinical Trials Unit, Institute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, B15 2TT, UK.
  • Mehanna H; Comprehensive Cancer Centre, King's College London, Guy's Campus, New Hunt's House, Room 2.36b, London, SE1 1UL, UK.
  • Watts C; Institute for Head and Neck Studies and Education, University of Birmingham, Birmingham, B15 2TT, UK.
  • Hills R; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, B15 2TT, UK.
  • Thomas I; Doll Building, CTSU, Nuffield Department of Population Health, University of Oxford, Old Road Campus, Roosevelt Drive, Oxford, OX3 7LF, UK.
  • Copland M; Centre for Trials Research, Cardiff University, Neuadd Meirionnydd, Heath Park Way, Cardiff, CF14 4YS, UK.
  • Bell S; Paul O'Gorman Research Centre, Gartnavel General Hospital, Glasgow, G12 0YN, UK.
  • Sebag-Montefiore D; Clinical Trials Research Unit (CTRU), Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, LS2 9JT, UK.
  • Jones R; Level 4 Bexley Wing St James Institute of Oncology, Leeds, LS9 7TF, UK.
  • Parmar MKB; Beatson West of Scotland Cancer Centre, Glasgow, UK.
  • Sydes MR; MRC Clinical Trials Unit at UCL, 90 High Holborn, London, WC1V 6LJ, UK.
Trials ; 23(1): 757, 2022 Sep 06.
Article in En | MEDLINE | ID: mdl-36068599
BACKGROUND: Late-phase platform protocols (including basket, umbrella, multi-arm multi-stage (MAMS), and master protocols) are generally agreed to be more efficient than traditional two-arm clinical trial designs but are not extensively used. We have gathered the experience of running a number of successful platform protocols together to present some operational recommendations. METHODS: Representatives of six UK clinical trials units with experience in running late-phase platform protocols attended a 1-day meeting structured to discuss various practical aspects of running these trials. We report and give guidance on operational aspects which are either harder to implement compared to a traditional late-phase trial or are specific to platform protocols. RESULTS: We present a list of practical recommendations for trialists intending to design and conduct late-phase platform protocols. Our recommendations cover the entire life cycle of a platform trial: from protocol development, obtaining funding, and trial set-up, to a wide range of operational and regulatory aspects such as staffing, oversight, data handling, and data management, to the reporting of results, with a particular focus on communication with trial participants and stakeholders as well as public and patient involvement. DISCUSSION: Platform protocols enable many questions to be answered efficiently to the benefit of patients. Our practical lessons from running platform trials will support trial teams in learning how to run these trials more effectively and efficiently.
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Full text: 1 Database: MEDLINE Main subject: Research Design / Data Management Type of study: Guideline / Qualitative_research Limits: Humans Country/Region as subject: Europa Language: En Year: 2022 Type: Article

Full text: 1 Database: MEDLINE Main subject: Research Design / Data Management Type of study: Guideline / Qualitative_research Limits: Humans Country/Region as subject: Europa Language: En Year: 2022 Type: Article