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Xlife Sciences with pleasing progress in the first half of 2022

Xlife Sciences AG / Key word(s): Half Year Results28-Sep-2022 / 07:01 CET/CESTRelease of an ad hoc announcement pursuant to Art. 53 LRThe issuer is solely responsible for the content of this announcement.Xlife Sciences (SIX: XLS) today published its results for the first half of 2022 ending 30 June 2022. Oliver R. B.

First and only biologic recommended for EU approval in patients with severe asthma with no phenotype or biomarker limitations

AstraZeneca’s Tezspire (tezepelumab) has been recommended for marketing authorisation in the European Union (EU) as an add-on therapy in patients 12 years and older with severe asthma who are inadequately controlled with high dose inhaled corticosteroids plus another medicinal product for maintenance treatment. The .

Tezspire recommended for approval in EU by CHMP for treatment of severe asthma

Tezspire recommended for approval in EU by CHMP for treatment of severe asthma
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