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Theriva Biologics — Third Quarter 2026 Earnings Summary

  • Net loss narrowed significantly to $6.7 million for the nine months ended September 30, 2026, compared to $21.7 million in the prior year period, driven by a 51% reduction in general and administrative expenses and a 76% drop in research and development costs following the completion of the VCN-01 Phase 2b PDAC trial and pause of SYN-004 expenses.
  • The Company completed the sale of its SYN-004 portfolio to Biossil Labs Inc. in October 2026, securing a $350,000 upfront payment with eligibility for up to $91 million in milestones and royalties, while retaining obligations to share 50% of future regulatory/sales milestones and 33 1/3% of royalties with PREV ABR LLC.
  • VIRAGE2 trial enrollment is on track to complete in Q4 2026, with initial pharmacodynamic and safety data anticipated in Q3 2027 to inform potential pivotal Phase 3 trials for metastatic PDAC; the Company also expects FDA interactions regarding a retinoblastoma trial design in Q1 2027.
  • Cash and cash equivalents stood at $8.5 million as of September 30, 2026, providing a runway into Q1 2027, while management continues to evaluate strategic alternatives to maximize stockholder value.
Company
THERIVA BIOLOGICS INC
Sector
Healthcare
Industry
Biotechnology