BioInvent releases Q2 2026 interim report highlighting clinical progress
The firm reports robust trial outcomes for its lead immunotherapy candidates and secures FDA Fast Track status for an ovarian cancer therapy.
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Clinical-stage biopharmaceutical company developing antibody-based cancer therapies
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In short: BioInvent secured FDA Fast Track for BI-1808 and reported strong clinical results for its cancer pipeline despite widening financial losses.
The firm reports robust trial outcomes for its lead immunotherapy candidates and secures FDA Fast Track status for an ovarian cancer therapy.
The FDA granted Fast Track for the anti-TNFR2 antibody in combination with pembrolizumab, after Phase 2a data showed 24% ORR and 56% DCR in platinum-resistant ovarian cancer.
BI-1206 showed 81% response rate in follicular lymphoma, and BI-1808 achieved 40% ORR in CTCL.
The combination showed 81% ORR in follicular lymphoma and lower serious adverse events (14%) versus SOC regimens.
Research company Bioinvent reports an operating result for the second quarter of 2026 at -125 million kronor (34.1).
Bioinvent has been granted fast track status for BI-1808 by the U.S. Food and Drug Administration (FDA), for the treatment of ovarian cancer in combination...
Detailed price information for Bioinvent International Ab (BOVNF) from The Globe and Mail including charting and trades.
Detailed price information for Bioinvent International Ab (BOVNF) from The Globe and Mail including charting and trades.
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