Logotype for Aligos Therapeutics Inc

Aligos Therapeutics (ALGS) Q1 2026 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Aligos Therapeutics Inc

Q1 2026 earnings summary

7 May, 2026

Executive summary

  • Focused on developing therapeutics for liver diseases and viral infections, with three clinical-stage candidates: pevifoscorvir sodium (HBV), ALG-055009 (MASH/obesity), and ALG-097558 (coronavirus).

  • Pevifoscorvir sodium received FDA Fast Track Designation for chronic HBV infection; Phase 2 B-SUPREME trial ongoing with positive interim analysis and DSMB recommendation to increase sample size.

  • Entered an exclusive license with Amoytop for pevifoscorvir sodium in Greater China, receiving $25M upfront and eligibility for up to $420M in milestones and royalties.

  • ALG-055009 showed positive Phase 2a results in MASH, with significant liver fat reduction and favorable safety profile; funding and out-licensing options under evaluation.

  • IND-enabling studies for ALG-170675 (ASO for HBV) are underway, with development costs in China funded by Amoytop.

Financial highlights

  • Revenue from customers was $2.8M for Q1 2026, up from $0.3M in Q1 2025, driven by a milestone payment from Amoytop.

  • Net loss for Q1 2026 was $23.0M, or $(2.21) per share basic, compared to net income of $43.1M, or $5.12 per share basic, in Q1 2025.

  • Research and development expenses increased 61% year-over-year to $23.4M, mainly due to higher clinical trial costs for pevifoscorvir sodium.

  • General and administrative expenses rose 27% to $6.4M, reflecting higher personnel and legal costs.

  • Cash, cash equivalents, and short-term investments totaled $54.9M as of March 31, 2026.

Outlook and guidance

  • Current cash and expected Amoytop upfront payment are projected to fund operations into Q4 2026.

  • Additional capital will be required to continue operations beyond Q4 2026; management is actively seeking further financing.

  • Topline data from the Phase 2 B-SUPREME study for pevifoscorvir sodium anticipated in 2027, with a second interim analysis for the HBeAg+ cohort expected in H2 2026.

  • Long-term post-treatment data from Phase 1 study to be presented at EASL 2026 Congress.

Partial view of Summaries dataset, powered by Quartr API
AI can get things wrong. Verify important information.
All investor relations material. One API.
Learn more