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23/03/25 Beursgangen: de drie IPO's om in 2025 in de gaten te houden
09/01/25 Pharmakonzern Stada vor milliardenschwerem Börsengang
11/09/24 Beteiligungsfirma GTCR erwägt laut Medienberichten milliardenschweren Stada-Kauf
26/07/24 Calliditas partner STADA receives European Commission decision for full approval of Kinpeygo® for the treatment of IgA Nephropathy
30/05/24 Calliditas partner STADA receives positive CHMP opinion recommending full approval for Kinpeygo[®] for the treatment of IgA nephropathy
29/05/24 Bio-Thera and STADA Reach Exclusive Agreement for BAT2506, a Proposed Golimumab Biosimilar, in the EU and UK
10/05/24 Xbrane and STADA partner with Valorum Biologics to commercialize ranibizumab biosimilar candidate in the US
14/03/24 Arzneikonzern Stada wächst - Finanzinvestoren prüfen Ausstieg
04/03/24 Xbrane has received additional subscription undertakings corresponding to approximately SEK 18.1 million in the Company's rights issue
10/11/23 Alvotech, Stada Get EU Panel Backing for Stelara Biosimilar
03/10/23 Calliditas announces filing with UK MHRA for Kinpeygo in IgA nephropathy
28/09/23 STADA and Calliditas announce the filing for full marketing authorization of Kinpeygo® in the EU
15/08/23 Calliditas Therapeutics announces full results from the NefIgArd Phase 3 trial published in The Lancet
25/07/23 STADA and Xbrane weigh options for ranibizumab biosimilar candidate
21/06/23 Xbrane announce U.S. FDA filing acceptance for a Lucentis® (ranibizumab) biosimilar candidate
26/05/23 STADA AND XBRANE LAUNCH XIMLUCI AS RANIBIZUMAB BIOSIMILAR IN GERMANY
26/05/23 STADA and Xbrane launch Ximluci® as ranibizumab biosimilar in Germany
26/04/23 STADA AND XBRANE SUPPLY XIMLUCI IN ENGLAND UNDER NHS CONTRACT
25/04/23 STADA and Xbrane supply Ximluci® (ranibizumab) in England under NHS contract
03/04/23 STADA and Xbrane launch ranibizumab to support patient access in Europe
23/02/23 AFR: STADA Arzneimittel AG: Vorabbekanntmachung über die Veröffentlichung von Finanzberichten gemäß § 114, 115, 117 WpHG
23/02/23 AFR: STADA Arzneimittel AG: Vorabbekanntmachung über die Veröffentlichung von Finanzberichten gemäß § 114, 115, 117 WpHG
08/02/23 European Biosimilar Regulatory Updates
02/02/23 Calliditas Receives Conditional Marketing Authorization from UK MHRA for Kinpeygo in IgA nephropathy
17/01/23 STADA and Xbrane obtain British approval for Ximluci® (ranibizumab) biosimilar referencing Lucentis®
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