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Get filing alertsRed Flags Detected
- Going Concern (worsened) — Going-concern language persists despite extended cash runway; substantial doubt remains about ability to continue operations beyond Q1 2027 without additional capital.
- Material Weakness (improved) — Material weaknesses in internal controls remediated as of December 31, 2024 and remain effective through December 31, 2025.
net income -$23.7M. Theriva cuts 7.5% of workforce, out-licenses SYN-020, extends cash runway to Q1 2027
Filed March 12, 2026 · Period ending December 31, 2025 · Compared to 10-K Mar 6, 2025 · ~2 min read
Key Changes
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Company implemented 32% workforce reduction (7 employees) in September 2025, incurring $520K severance to focus on VCN-01 development and business development. Expected to save $1.8M annually but signals capital preservation mode.
Business: Workforce reduction verify on EDGAR → -
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VIRAGE Phase 2b trial showed VCN-01 plus chemotherapy improved median overall survival to 10.8 vs 8.6 months (p=0.0546), with statistically significant PFS improvement (7.0 vs 4.6 months, p=0.0105). EMA endorsed multi-dose Phase 3 design.
Business: VIRAGE results verify on EDGAR → -
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Out-licensed SYN-020 to Rasayana for $300K upfront plus potential $38M in milestones and low-to-mid single-digit royalties. Rasayana assumes all development costs, freeing capital for oncology focus.
Business: SYN-020 license verify on EDGAR →
2 more material changes 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 · Jun 8, 2026 · How we verify