The trial consists of a series of parallel multi-centre single arm phase II trial arms, each testing an experimental targeted drug in a population stratified by multiple pre-specified actionable target putative biomarkers. The primary objective is to evaluate whether there is a signal of activity in each drug-(putative)biomarker cohort separately. A Bayesian adaptive design is adopted to achieve this objective and statistical details are given in the Protocol.
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Objective response (OR)
Timeframe: From baseline until disease progression, assessed up to 18 months.
Progression-free survival time (PFS)
Timeframe: From date of commencement of trial treatment to date of CT scan when progressive disease first recorded or date of death without previously recorded progression, assessed up to 18 months.
Durable clinical benefit (DCB)
Timeframe: From baseline until the first scan after 24 weeks showing the patient free of disease progression.