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Swedish Orphan Biovitrum AB: Bulletin from Swedish Orphan Biovitrum (Sobi)'s Annual General Meeting (AGM) - Vimarsana News

Swedish Orphan Biovitrum AB: Bulletin from Swedish Orphan Biovitrum (Sobi)'s Annual General Meeting (AGM)

STOCKHOLM, May 9, 2023 /PRNewswire/ -- The Sobi® AGM was convened today on 9 May 2023. At the AGM, the shareholders, in accordance with the proposed resolutions, resolved as follows: Adoption

Notice of Annual general meeting in Swedish Orphan Biovitrum AB (publ) - Vimarsana News

Notice of Annual general meeting in Swedish Orphan Biovitrum AB (publ)

The shareholders in Swedish Orphan Biovitrum AB Reg. No. 556038-9321, are hereby summoned to the Annual General Meeting , to be held on Tuesday, 9 May 2023 at 15.00 at IVA Konferenscenter, Grev... | March 30, 2023

LEO Pharma A/S: LEO Pharma Announces European Commission Approval of Adtralza (tralokinumab) for the Treatment of Moderate-to-Severe Atopic Dermatitis in Adolescents - Vimarsana News

LEO Pharma A/S: LEO Pharma Announces European Commission Approval of Adtralza (tralokinumab) for the Treatment of Moderate-to-Severe Atopic Dermatitis in Adolescents

Adtralza, a biologic that targets and neutralizes the interleukin (IL)-13 cytokine1, is now approved in Europe for adolescents with moderate-to-severe atopic dermatitis.2 NOT FOR DISTRIBUTION

LEO Pharma receives positive CHMP opinion of Adtralza - Vimarsana News

LEO Pharma receives positive CHMP opinion of Adtralza

Therapy is for the treatment of adolescents with moderate-to-severe atopic dermatitis - News - PharmaTimes

LEO Pharma A/S: LEO Pharma Receives Positive CHMP Opinion of Adtralza (tralokinumab) for the Treatment of Adolescents With Moderate-to-Severe Atopic Dermatitis - Vimarsana News

LEO Pharma A/S: LEO Pharma Receives Positive CHMP Opinion of Adtralza (tralokinumab) for the Treatment of Adolescents With Moderate-to-Severe Atopic Dermatitis

Positive CHMP opinion recommends extending use of Adtralza (tralokinumab) to adolescents (12-17 years old) in the European Union (EU) Recommendation supported by data from the Phase 3 ECZTRA