Adverse Effects44% of patients experienced treatment-related adverse events leading to discontinuation, which is higher than the 38% for mirv+bev.
Clinical PerformanceSafety data was pooled, making it difficult to assess the performance of the RP2D.
Stock PerformanceShares are down -30% YTD, largely due to the lack of clinical catalysts, and are expected to remain range bound until nearer the Part 2 readout.