Logotype for BeyondSpring Inc

BeyondSpring (BYSI) Q3 2025 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for BeyondSpring Inc

Q3 2025 earnings summary

12 Nov, 2025

Executive summary

  • Plinabulin, a first-in-class cancer therapy, demonstrated an 85% disease control rate in metastatic NSCLC patients post PD-1/L1 inhibitors, with a median PFS of 7.0 months and a 12-month OS rate of 79% in Phase 2, and is advancing in multiple late-stage and investigator-initiated studies, with a pipeline of preclinical immune agents.

  • Completed a strategic divestiture of SEED Therapeutics, reclassifying its operations as discontinued and recording a $7.0 million gain on sale of subsidiary interests; BeyondSpring’s ownership in SEED to decrease to approximately 13.62% by end of 2026.

  • SEED, with a 38% equity share, completed $30 million Series A-3 financing, received IND clearance for its RBM39 degrader program from US FDA and China NMPA, and was named a finalist for the 2025 Prix Galien USA “Best Start-Up” Award.

  • No product sales revenue; collaboration revenue from Eli Lilly through SEED, with deferred revenue from Hengrui collaboration.

Financial highlights

  • Net loss from continuing operations was $1.7 million for Q3 2025, down from $2.2 million in Q3 2024; net loss for nine months was $6.2 million, down from $6.9 million year-over-year.

  • Consolidated net loss for Q3 2025 was $4.9 million, and $8.4 million for the nine months, both improved from prior year periods.

  • Cash and cash equivalents at September 30, 2025 were $12.5 million, up from $2.9 million at December 31, 2024, with no outstanding debt.

  • R&D expenses for Q3 2025 were $1.0 million, up from $0.6 million in Q3 2024; G&A expenses for Q3 2025 were $0.8 million, down from $1.7 million in Q3 2024.

  • Accumulated deficit decreased to $406.3 million from $407.4 million at year-end 2024.

Outlook and guidance

  • Expects continued significant R&D and operating losses as clinical programs advance; current resources expected to fund operations for at least 12 months.

  • Additional capital will be needed for future operations, with ongoing evaluation of financing, licensing, and partnership options.

  • Plinabulin continues to show promise as an immune-modulating therapy for NSCLC and other cancers, with ongoing late-stage clinical development.

  • SEED’s RBM39 degrader is entering clinical development for Ewing sarcoma and other RBM39-dependent cancers.

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