BioInvent Presents Impressive Response Data from Ongoing Phase 2a Trial of Triple Combination BI-1206, Rituximab, and Calquence in r/r NHL at ASH 2025

Core Insights - BI-1206 shows potential to overcome resistance mechanisms to rituximab in treating non-Hodgkin's lymphoma [1] - 47% of patients achieved complete responses (CR), with an overall response rate of 80% [1] - The safety profile is favorable, with 87% of adverse events being mild or moderate, and no treatment-related discontinuations [1] - The safety run-in portion of the study is complete, showing no significant differences in safety or efficacy between the two dose levels [1] - The signal-seeking expansion phase of the study is currently ongoing [1] Company Overview - BioInvent International AB is focused on discovering and developing novel and first-in-class immune-modulatory antibodies for cancer immunotherapy [1] - The company presented new data from its ongoing trial of BI-1206 at the 2025 American Society of Hematology Annual Meeting [1] Industry Context - Anti-CD20 antibodies, such as rituximab, are critical for the treatment of non-Hodgkin's lymphoma [1]