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The Ecosystem: European Innovation Council uncouples grant and equity funding for start-ups

From 2024, start-ups will no longer be able to bid for grant-first funding under the European Innovation Council (EIC) Accelerator programme. Instead, this option will be integrated into the programmeโ€™s blended finance offer, in a recognition that many more applicants would like to separate decisions about grant funding and equity investment.
City Of United Kingdom Anders Kronborg Alex Chalkley Piotr Dabkowski Resother Pharma

Resolutions from Aqilion Annual General Meeting 2023

Resolutions from Aqilion Annual General Meeting 2023Helsingborg, June 1, 2023 – AQILION AB (publ) held its Annual General Meeting today, at which the meeting decided in accordance with the proposals presented. For more detailed information on the content of the resolutions, please see the full notice to the An...
Skane Lan Roland Andersson Anders Kronborg Bertil Toreson Andreas Segerros Sarah Fredriksson

LEO Pharma Announces FDA Approval of Adbry™ (tralokinumab) as the First and Only Treatment Specifically Targeting IL-13 for Adults With Moderate-to-Severe Atopic Dermatitis

LEO Pharma A/S, a global leader in medical dermatology, announced today that the U.S. Food and Drug Administration (FDA) has approved Adbryโ„ข (tralokinumab) for the treatment of moderate-to-severe atopic dermatitis in adults 18 years or older whose disease is not adequately controlled with topical prescription therapies or when those therapies are not advisable.
United States United Arab Emirates United Kingdom Great Britain Jonathan Silverberg Anders Kronborg

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LEO Pharma Announces FDA Approval of Adbry (tralokinumab) as the First and Only Treatment Specifically Targeting IL-13 for Adults With Moderate-to-Severe Atopic Dermatitis

Adbry is the first biologic launched by LEO Pharma in the United States and is expected to be available in pharmacies by February 2022. Tralokinumab is marketed outside of the U.S. under the
United States United Arab Emirates United Kingdom Great Britain Jonathan Silverberg Anders Kronborg

LEO Pharma announces FDA approval of Adbry™ (tralokinumab) as the first and only treatment specifically targeting IL-13 for adults with moderate-to-severe atopic dermatitis

LEO Pharma A/S, a global leader in medical dermatology, announced today that the U.S. Food and Drug Administration (FDA) has approved Adbry™ (tralokinumab) ...
United States United Arab Emirates United Kingdom Great Britain Jonathan Silverberg Leo Pharma

LEO Pharma's FDA nod adds a challenger to Dupixent's dominance in eczema

With FDA approval for its atopic dermatitis drug Adbry, LEO Pharma will reach the U.S market ahead of an Eli Lilly atopic dermatitis drug that addresses the same target. LEO will also able to offer patients an alternative to the blockbuster Sanofi/Regeneron Pharmaceuticals drug Dupixent.
United Arab Emirates United Kingdom Great Britain Anders Kronborg Eli Lilly European Union

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