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In October 2024, the U.S. Food and Drug Administration (FDA) approved SELARSDI™ for all indications matching the reference product Stelara® (ustekinumab) and has granted a provisional determination of...
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Matvæla- og lyfjastofnun Bandaríkjanna (FDA) hefur heimilað notkun Selarsdi fyrir allar sömu ábendingar og frumlyfsins StelaraFDA hefur jafnframt tilkynnt að öll lyfjaform Selarsdi verði útskiptanleg...
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In October 2024, the U.S. Food and Drug Administration (FDA) approved SELARSDI™ for all indications matching the reference product Stelara® (ustekinumab) and has granted a provisional determination of...
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REYKJAVIK, Iceland and PARSIPPANY, N.J., Feb. 18, 2025 (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO), a global biotech company specializing in the development and manufacture of biosimilar medicines...
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Alvotech (NASDAQ: ALVO) og samstarfsaðili þess Teva Pharmaceuticals, bandarískt dótturfélag Teva Pharmaceutical Industries Ltd. tilkynntu í dag að Matvæla- og lyfjastofnun Bandaríkjanna (FDA) hafi...
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Alvotech (NASDAQ: ALVO), a global biotech company specializing in the development and manufacture of biosimilar medicines for patients worldwide, and Teva Pharmaceuticals, a U.S. affiliate of Teva...
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Alvotech (NASDAQ: ALVO) og samstarfsaðili þess Teva Pharamceuticals, bandarískt dótturfélag Teva Pharmaceutical Industries Ltd. tilkynntu í dag að Matvæla- og lyfjastofnun Bandaríkjanna (FDA) hafi...
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Alvotech (NASDAQ: ALVO), a global biotech company specializing in the development and manufacture of biosimilar medicines for patients worldwide, and Teva Pharmaceuticals, a U.S. affiliate of Teva...
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REYKJAVIK, Iceland and PARSIPPANY, N.J., Jan. 27, 2025 (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO), a global biotech company specializing in the development and manufacture of biosimilar medicines...
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Stefnt er að því að birting árshluta- og ársuppgjörs Alvotech og aðalfundur félagsins fari fram sem hér segir á árinu 2025: Árshlutauppgjör fjórða ársfjórðungs 2024 og ársuppgjör 202426....