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BioArcticAB

@bioarcticab

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Biopharma. Neurodegenerative diseases. Corporate account publishing press releases for IR. GDPR info: https://t.co/1ZcLRn6LIh

Stockholm
Joined February 2021
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@bioarcticab
BioArcticAB
1 year
PRESS RELEASE: FDA accepts filing of Leqembi[®] (lecanemab-irmb) sBLA for IV maintenance dosing for the treatment of early Alzheimer’s Disease.
bioarctic.com
Stockholm, Sweden, June 10, 2024 – BioArctic AB’s (publ) (Nasdaq Stockholm: BIOA B) partner Eisai announced today that that the U.S. Food and Drug Administration (FDA) has accepted Eisai’s Suppleme...
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@EisaiUS
Eisai US
1 year
We’re pleased to share an update on the subcutaneous (SC) development program of our treatment for early #AlzheimersDisease (AD).
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@bioarcticab
BioArcticAB
1 year
PRESS RELEASE: Eisai initiates rolling Biologics License Application to US FDA for Leqembi® (lecanemab-irmb) for subcutaneous maintenance dosing.
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bioarctic.com
Stockholm, Sweden, May 15, 2024 – BioArctic AB's (publ) (Nasdaq Stockholm: BIOA B) partner Eisai announced today that they have initiated the rolling submission of a Biologics License Application...
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@bioarcticab
BioArcticAB
2 years
Press release: BioArctic and Eisai sign research evaluation agreement regarding a potential new treatment combining BioArctic’s proprietary BrainTransporter™ technology with an undisclosed Alzheimer drug candidat.
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@bioarcticab
BioArcticAB
2 years
Press release: BioArctic publishes the Annual Report for 2023
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@bioarcticab
BioArcticAB
2 years
Press release: The Nomination Committee’s proposal for the election of Board members and Chairperson of the Board in BioArctic AB.
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@bioarcticab
BioArcticAB
2 years
PRESS RELEASE: BioArctic’s focus on Sustainable Innovation qualifies company for new ESG Responsibility Index at Nasdaq Stockholm.
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@bioarcticab
BioArcticAB
2 years
PRESS RELEASE: Submission of Leqembi® (lecanemab-irmb) sBLA for IV maintenance dosing for the treatment of early Alzheimer’s disease to the U.S. FDA completed.
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@bioarcticab
BioArcticAB
2 years
Press release: Lecanemab deliberations at the CHMP regarding the Marketing Authorisation Application in the EU have been rescheduled due to procedural reasons.
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