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BioInvent International (BINV) investor relations material
BioInvent International Q3 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Portfolio reprioritized to focus on BI-1808 and BI-1206, both in Phase II trials for liquid and solid tumors, with early-stage programs paused.
BI-1808 shows 100% disease control and 45% objective response in CTCL; BI-1206 initiated pivotal Phase 2a in first-line NSCLC and uveal melanoma.
Regulatory milestones include FDA Fast Track and Orphan Drug Designations for BI-1808 in T-cell lymphomas.
Board change: Vincent Osipo/Ossipow stepped down after nearly 10 years.
Accelerated clinical progress has led to earlier-than-expected data readouts.
Financial highlights
Q3 2025 net sales: SEK 3.3 million, down from SEK 12.8 million in Q3 2024; Jan–Sep 2025 net sales: SEK 223.5 million, up from SEK 23.3 million, mainly from a $20 million royalty rights deal.
Q3 2025 operating costs: SEK 137 million; Jan–Sep 2025: SEK 446 million.
Q3 2025 loss after tax: SEK -129.2 million; Jan–Sep 2025: SEK -207.1 million, improved from SEK -312.5 million.
Liquid funds and investments at end of Sep 2025: SEK 690.5 million; financing secured into Q1 2027.
Cash flow from operating activities Jan–Sep 2025: SEK -157.2 million, improved from SEK -282.2 million.
Outlook and guidance
Multiple data updates for BI-1808 and BI-1206 expected in 2025, including Phase II-A monotherapy and combination data.
First data from BI-1206 first-line solid tumor study expected in H2 2026.
Potential for pivotal studies in 2026 for BI-1808 monotherapy in T cell lymphoma and BI-1206 in NHL.
Focus on partnering opportunities as mature data emerges in 2026.
Sufficient funding to reach upcoming value inflection points.
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