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WKN: A3DK8U | ISIN: LU2458332611 | Ticker-Symbol: Z45
Stuttgart
22.01.25
08:04 Uhr
12,650 Euro
0,000
0,00 %
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ALVOTECH Chart 1 Jahr
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23.12.24Alvotech - 6-K, Report of foreign issuer2
23.12.24Alvotech Added to Nasdaq Biotech Index Effective Monday December 23, 2024300Addition is part of the annual reconstitution of the Nasdaq Biotech Index (NBI)Inclusion criteria include minimum market capitalization and daily trading volumes Alvotech (NASDAQ: ALVO), a global...
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13.11.24Alvotech - 6-K, Report of foreign issuer1
13.11.24Alvotech GAAP EPS of -$0.63, revenue of $339M7
13.11.24Alvotech S.A.: Alvotech Reports Financial Results for the First Nine Months of 2024195Total 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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12.11.24Alvotech's Earnings Outlook8
05.11.24EMA accepts Alvotech and Advanz Pharma's AVT05 MAA4
ALVOTECH Aktie jetzt für 0€ handeln
04.11.24Alvotech: European Medicines Agency Confirms Acceptance of Marketing Authorization Application for AVT05, a Proposed Biosimilar to Simponi (golimumab)248REYKJAVIK, 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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04.11.24Alvotech - 6-K, Report of foreign issuer1
24.10.24Alvotech's SWOT analysis: biosimilar powerhouse stock faces growth hurdles4
23.10.24FDA approves Alvotech and Teva's SELARSDI for new indications19
22.10.24Teva, Alvotech get expanded FDA approval for Stelara biosimilar16
22.10.24Alvotech And Teva Pharmaceuticals Announce Expansion Of SELARSDI's Indications391PETAH 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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22.10.24Teva 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)555Approval 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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22.10.24Alvotech 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)366Approval 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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22.10.24Alvotech - 6-K, Report of foreign issuer9
10.10.24Alvotech - 6-K, Report of foreign issuer5
10.10.24Alvotech application for Prolia/Xgeva biosimilar accepted by EMA7
10.10.24Alvotech: European Medicines Agency Confirms Acceptance of Marketing Application for AVT03, a Proposed Biosimilar to Prolia and Xgeva461Alvotech (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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25.09.24Alvotech Initiates Confirmatory Patient Study for AVT16, a Proposed Biosimilar to Entyvio379Alvotech 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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