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Get filing alertsTango posts 92% response rate in PDAC combo trial; raises $651M to fund Phase 3
Filed August 11, 2026 · Period ending June 30, 2026 · Compared to 10-Q Aug 5, 2025 · ~2 min read
Key Changes
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Vopimetostat + daraxonrasib achieved 92% objective response rate in MTAP-deleted pancreatic cancer (11 of 12 patients) and 100% in NSCLC (3 of 3), with 90% six-month progression-free survival in PDAC; company plans Phase 3 randomized trial in front-line setting.
MD&A: vopimetostat + daraxonrasib Phase 1/2 data verify on EDGAR → -
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Company deprioritized TNG260 (CoREST inhibitor) due to limited clinical benefit and halted TNG961 (HBS1L degrader) development, shutting down both trials to focus resources on the PRMT5 pipeline; direct R&D spend on TNG260 fell 26% and TNG961 fell 96% YoY.
MD&A: TNG260 and TNG961 deprioritization verify on EDGAR → -
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Net loss for Q2 2026 was $55.3M (diluted EPS -$0.37), widening 42.4% from $38.8M in Q2 2025, driven by higher R&D spend on vopimetostat (up 121% to $12.3M) and near-doubling of G&A expense to $22.6M, while collaboration revenue fell to zero following Gilead research-term truncation in August 2025.
MD&A: net loss verify on EDGAR →
1 more material change behind this preview — plus the full narrative summary, section-by-section diffs against the prior filing, and verbatim quotes with EDGAR citations.
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Figures/quotes linked to EDGAR · Narrative written by AI · Aug 18, 2026 · How we verify