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2023	Alvotech et Stada obtiennent le soutien du comité de l'UE pour le biosimilaire de Stelara	MT
2021	Sanofi cède 16 produits de santé grand public à l'allemand Stada	DJ

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Calliditas partner STADA receives positive CHMP opinion recommending full approval for Kinpeygo[®] for the treatment of IgA nephropathy	30/05	AQ
Bio-Thera and STADA Reach Exclusive Agreement for BAT2506, a Proposed Golimumab Biosimilar, in the EU and UK	29/05	AQ
Xbrane and STADA partner with Valorum Biologics to commercialize ranibizumab biosimilar candidate in the US	10/05	AQ
Xbrane has received additional subscription undertakings corresponding to approximately SEK 18.1 million in the Company's rights issue	04/03	AQ
Calliditas announces filing with UK MHRA for Kinpeygo in IgA nephropathy	03/10/23	AQ
STADA and Calliditas announce the filing for full marketing authorization of Kinpeygo® in the EU	28/09/23	AQ
Calliditas Therapeutics announces full results from the NefIgArd Phase 3 trial published in The Lancet	15/08/23	AQ
STADA and Xbrane weigh options for ranibizumab biosimilar candidate	25/07/23	AQ
Xbrane announce U.S. FDA filing acceptance for a Lucentis® (ranibizumab) biosimilar candidate	21/06/23	AQ
STADA AND XBRANE LAUNCH XIMLUCI AS RANIBIZUMAB BIOSIMILAR IN GERMANY	26/05/23	AQ
STADA and Xbrane launch Ximluci® as ranibizumab biosimilar in Germany	26/05/23	AQ
STADA AND XBRANE SUPPLY XIMLUCI IN ENGLAND UNDER NHS CONTRACT	26/04/23	AQ
STADA and Xbrane supply Ximluci® (ranibizumab) in England under NHS contract	25/04/23	AQ
STADA and Xbrane launch ranibizumab to support patient access in Europe	03/04/23	AQ
AFR: STADA Arzneimittel AG: Preliminary announcement of the publication of financial reports according to Articles 114, 115, 117 of the WpHG [the German Securities Act]	23/02/23	EQ
AFR: STADA Arzneimittel AG: Preliminary announcement of the publication of financial reports according to Articles 114, 115, 117 of the WpHG [the German Securities Act]	23/02/23	EQ
European Biosimilar Regulatory Updates	08/02/23	AQ
Calliditas Receives Conditional Marketing Authorization from UK MHRA for Kinpeygo in IgA nephropathy	02/02/23	AQ
STADA and Xbrane obtain British approval for Ximluci® (ranibizumab) biosimilar referencing Lucentis®	17/01/23	AQ
STADA And Xbrane Announce Approval Of Ranibizumab Biosimilar In Europe	15/11/22	AQ

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