Abstract

BI 1701963 is a small-molecule protein–protein interaction inhibitor, which prevents KRAS activation by binding to the catalytic site of SOS1. This multicentre phase I first-in-human trial is evaluating BI 1701963 as monotherapy (mono tx) or in combination with trametinib in adults with KRAS-mutated solid tumours. Here, we report preliminary results from the mono tx arm, which aims to determine the maximum tolerated dose (MTD) and/or recommended phase II dose of BI 1701963, based on dose-limiting toxicities (DLTs).

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