| Literature DB >> 29108786 |
J A Harrington1, T C Hernandez-Guerrero1, B Basu2.
Abstract
The process of anti-cancer drug development is complex, with high attrition rates. Factors that may optimise this process include well-constructed and relevant pre-clinical testing and use of biomarkers for patient selection. However, the design of early phase clinical trials will probably play a vital role in both the robust clinical investigation of new targeted therapies and in streamlining drug development. In this overview, we assess current concepts in phase I clinical trials, highlighting issues and opportunities to improve their meaningfulness. The particular challenge of how to design combination trials is addressed, with focus on the potential of new adaptive and model-based designs. CrownEntities:
Keywords: Adaptive design; biomarker; dose escalation methods; early phase clinical trials; phase I trials
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Year: 2017 PMID: 29108786 DOI: 10.1016/j.clon.2017.10.005
Source DB: PubMed Journal: Clin Oncol (R Coll Radiol) ISSN: 0936-6555 Impact factor: 4.126