Cellid Q1 2026: Liquidity Concerns, COVID Vaccine Setback, Pipeline Progress


  • Q1 2026 revenue: 3.2 billion won (up from 1.6 billion YoY), operating loss narrowed to 1.6 billion won (from 2.7 billion).
  • Current liabilities (34.9B) exceed current assets (22.9B), raising liquidity risk. Cash dropped sharply to 10.5B from 22.4B at year-end 2025.
  • High debt burden: borrowings 29.4B, financial guarantees 42.3B (related to Magok HQ PF loan).
  • COVID-19 vaccine AdCLD-CoV19-1 OMI phase 3 dosing completed (Nov 2024), awaiting final results.
  • IND for variant vaccine AdCLD-CoV19-1 LP.8.1 phase 2 was rejected on May 8, 2026.
  • BVAC-C investigator-initiated trial shows complete/partial responses; presented at ASCO, SGO, AOS.
  • BVAC-E6E7 (head and neck cancer) phase 1/2a approved (Nov 2024), patient recruitment started.
  • LG Chem license-out for BVAC-Neo continues (upfront 1B, milestones up to 183.5B, plus royalties).
  • Three ongoing lawsuits totaling ~4.8B won.
  • R&D expenses 0.84B (down from 1.46B YoY), continued capitalization of development costs (289B).
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KOSDAQ Filing Information


  • Filing: Quarterly Report (2026.03)
  • Company: Cellid (299660)
  • Submission: Cellid Co., Ltd.
  • Receipt: 05-15-2026