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WKN: A3DK8U | ISIN: LU2458332611 | Ticker-Symbol: Z45
Stuttgart
21.11.24
08:09 Uhr
11,650 Euro
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14.11.Alvotech SA reports results for the quarter - Earnings Summary2
13.11.Alvotech - 6-K, Report of foreign issuer1
13.11.Alvotech GAAP EPS of -$0.63, revenue of $339M6
13.11.Alvotech S.A.: Alvotech Reports Financial Results for the First Nine Months of 2024158Total Revenues in the first nine months of 2024 increased by $300 million compared to same period in 2023, to $339 million, with Q3 revenues contributing $103 millionProduct revenues in the first nine...
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12.11.Alvotech's Earnings Outlook7
05.11.EMA accepts Alvotech and Advanz Pharma's AVT05 MAA4
04.11.Alvotech: European Medicines Agency Confirms Acceptance of Marketing Authorization Application for AVT05, a Proposed Biosimilar to Simponi (golimumab)206REYKJAVIK, Iceland and LONDON, Nov. 04, 2024 (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO), a global biotech company specializing in the development and manufacture of biosimilar medicines for patients...
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04.11.Alvotech - 6-K, Report of foreign issuer1
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24.10.Alvotech's SWOT analysis: biosimilar powerhouse stock faces growth hurdles4
23.10.FDA approves Alvotech and Teva's SELARSDI for new indications19
22.10.Teva, Alvotech get expanded FDA approval for Stelara biosimilar15
22.10.Alvotech And Teva Pharmaceuticals Announce Expansion Of SELARSDI's Indications340PETAH TIKVA (dpa-AFX) - Alvotech (ALVO) and Teva Pharmaceuticals, a U.S. affiliate of Teva Pharmaceutical Industries Ltd. (TEVA), announced the FDA has approved SELARSDI in a new presentation...
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22.10.Teva Pharmaceutical Industries Ltd: Alvotech and Teva Announce U.S. FDA Approval of Additional Presentation of SELARSDI (ustekinumab-aekn), Expanding its Label to Include Further Indications Approved for Reference Product, Stelara® (ustekinumab)470Approval of SELARSDI 130 mg/26 mL in a single-dose vial for intravenous infusion expands label to include treatment of adults with Crohn's disease and ulcerative colitisThe FDA previously approved SELARSDI...
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22.10.Alvotech and Teva Announce U.S. FDA Approval of Additional Presentation of SELARSDI (ustekinumab-aekn), Expanding its Label to Include Further Indications Approved for Reference Product, Stelara (ustekinumab)305Approval of SELARSDI 130 mg/26 mL in a single-dose vial for intravenous infusion expands label to include treatment of adults with Crohn's disease and ulcerative colitisThe FDA previously approved...
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22.10.Alvotech - 6-K, Report of foreign issuer9
10.10.Alvotech - 6-K, Report of foreign issuer5
10.10.Alvotech application for Prolia/Xgeva biosimilar accepted by EMA7
10.10.Alvotech: European Medicines Agency Confirms Acceptance of Marketing Application for AVT03, a Proposed Biosimilar to Prolia and Xgeva395Alvotech (NASDAQ: ALVO), a global biotech company specializing in the development and manufacture of biosimilar medicines for patients worldwide, announced today that the European Medicines Agency...
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25.09.Alvotech Initiates Confirmatory Patient Study for AVT16, a Proposed Biosimilar to Entyvio318Alvotech is one of two companies known to have initiated a global or multi-country confirmatory patient study for a biosimilar candidate to Entyvio®Sales of Entyvio (vedolizumab) were about $5.4 billion...
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26.08.Alvotech to Participate in the Morgan Stanley 22nd Annual Global Healthcare Conference2
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