HIGHLIGHTS
- What: The aim of the IMPRESS-Norway trial is to facilitate patient access to commercially available targeted anticancer therapies, and to describe anti-tumour activity and toxicity of targeted therapies. The trial is still recruiting patients, and the final data_analysis will be presented at the later time point. This study reports on the primary endpoint of the IMPRESS-Norway trial per October 1, 2023. Primary study endpoints are: 1) percentage of the patients included in the trial based on their molecular profile, and 2) disease control rate (DCR) defined as objective complete response (CR), partial response (PR . . .

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