FDA Fast Track Designation for BI-1808 for the Treatment of Ovarian Cancer
“Receiving FDA Fast Track Designation for BI-1808 in ovarian cancer is an important milestone that reflects the significant unmet medical need in this difficult-to-treat disease and the strength of the clinical signals we have generated to date,” said Martin Welschof, Chief Executive Officer of BioInvent. “The data we have presented across both high-grade serous and clear cell subtypes underscore the potential of targeting TNFR2 to meaningfully enhance the activity of PD-1 inhibitors in tumors where these agents have historically shown limited benefit. This designation validates our development strategy and strengthens our commitment to advancing BI-1808 as a new treatment option for patients with ovarian cancer.”
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