Alvotech and Teva Secure FDA Approval for SELARSDI

Alvotech (ALVO) has released an update.

Alvotech and Teva Pharmaceuticals have received U.S. FDA approval for a new intravenous presentation of SELARSDI, enhancing its use for Crohn’s disease and ulcerative colitis in adults. This approval aligns SELARSDI’s indications with the reference product Stelara, with a U.S. launch anticipated in the first quarter of 2025. The move is part of Alvotech and Teva’s strategic efforts to expand access to biosimilar medicines in the U.S. market.

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