•
in mil. unless spec.•
in mil. unless spec.•
in mil. unless spec.•
in mil. unless spec.•
in mil. unless spec.•
in mil. unless spec.More than 75% of Leqembi®-treated patients remained stable and nearly 7% improved over an average of 17 months of treatment in real-world LEADER study data presented at AAIC® 2026
BioArctic and Lilly sign research and collaboration agreement combining Lilly compound with BioArctic's BrainTransporter™ technology
Number of shares and votes in BioArctic AB (publ) as of May 29, 2026
Bulletin from the Annual General Meeting in BioArctic AB (publ)
BioArctic AB (publ) (BRCTF) Q1 2026 Earnings Call Transcript
BioArctic Interim Report for the period January - March 2026
Invitation to presentation of BioArctic's first quarter report for January - March 2026 on May 20 at 9:30 a.m. CET
Number of shares and votes in BioArctic AB (publ) as of February 27, 2026
BioArctic AB (publ) (BRCTF) Q4 2025 Earnings Call Transcript
BioArctic Interim Report for the period October - December 2025
Invitation to presentation of BioArctic's fourth quarter report for October - December 2025 on February 18 at 9.30 a.m. CET
Leqembi included in China's commercial insurance innovative drug list
New data on lecanemab to be presented at CTAD conference
Leqembi® approved for IV maintenance treatment in the United Kingdom
BioArctic AB (publ) (BRCTF) Q3 2025 Earnings Call Transcript
Interim Report for the period July - September 2025: BioArctic
Health Canada Grants Authorization for Leqembi® (lecanemab)
Leqembi® Iqlik™ (lecanemab-irmb) maintenance treatment launched in the U.S.
BioArctic's founders intend to divest minor part of their shareholding
Rolling sBLA initiated to the U.S. FDA for Leqembi® Iqlik™ (lecanemab-irmb) as a subcutaneous starting dose for the treatment of early Alzheimer's disease under Fast Track status