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Active Biotech Interim Report Q3 2026

Press Release
Regulatory

EVENTS DURING THE THIRD QUARTER

  • First patient dosed in the amended HO172 clinical study of tasquinimod in myelofibrosis (July 24)
  • Active Biotech expanded US collaboration to advance tasquinimod clinical development in myelofibrosis (August 18)
  • Active Biotech announced that global patent protection for laquinimod has been strengthened with Patent Grant in Japan (September 30)

EVENTS AFTER THE END OF THE PERIOD

  • First cohort under amended protocol successfully completed safety evaluation in HOVON 172 MF clinical study of tasquinimod in myelofibrosis (October 13)

FINANCIAL SUMMARY

SEK M Jul-Sep Jan-Sep Full year
2026 2025 2026 2025 2025
Net sales – – – – –
Operating profit/loss -8,5 -6.0 -27.3 -28.5 -37.6
Profit/loss after tax -8,3 -6.0 -26.8 -28.2 -37.3
Earnings per share (SEK) -0,32 -0.49 -1,02 -2.29 -2.77
Cash and cash equivalents (at close of period) 36.3 9.1 65.1

The report is also available at www.activebiotech.com
The information was submitted, through the agency of the contact person below, for public disclosure on 2026-11-05 at 08:30 CEST.