In October 2024, the U.S. Food and Drug Administration (FDA) approved SELARSDIâ„¢ for all indications matching the reference ...
In October 2024, the U.S. Food and Drug Administration (FDA) approved SELARSDIâ„¢ for all indications matching the reference product Stelara® (ustekinumab) and has granted a provisional ...
The FDA has provisionally determined that SELARSDI will be interchangeable with the reference biologic Stelara®, following the expiration of exclusivity for the first interchangeable biosimilar ...
In October 2024, the U.S. Food and Drug Administration (FDA) approved SELARSDI â„¢ for all indications matching the reference product Stelara ® (ustekinumab) and has granted a provisional determination ...
In October 2024, the FDA approved the biosimilar SELARSDIâ„¢ (ustekinumab-aekn), manufactured by Teva Pharmaceuticals in partnership with Alvotech, for various conditions similar to those treated ...
Teva Pharmaceuticals (TEVA) and Alvotech (ALVO) announced the availability of SELARSDI injection in the U.S., a biosimilar to Stelara for the ...
In February 2025, Teva Pharmaceuticals and Alvotech announced the U.S. launch of SELARSDIâ„¢ (ustekinumab-aekn), a biosimilar to Stelara® (ustekinumab), following FDA approval and a provisional ...
Teva Pharmaceuticals and Alvotech said on Friday they have launched a biosimilar to Johnson & Johnson's autoimmune drug Stelara in the United States, the second in a wave of near-copies of the ...
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