Johnson & Johnson (J&J) has received US Food and Drug Administration (FDA) approval for its interleukin 23 inhibitor, Tremfya ...
Johnson & Johnson developed the dual-acting monoclonal ... In January, 2025, J&J’s nasal spray Spravato secured a label expansion from the FDA for use as a single agent in adults with major depressive ...
FDA approved Johnson & Johnson’s Tremfya as the first IL-23 inhibitor with both SC and IV induction options for Crohn’s disease. Tremfya sales reached $3.67 billion in 2024, marking a 17% year ...
The company states: “Johnson & Johnson ... active Crohn’s disease, CD, a chronic inflammatory condition of the gastrointestinal tract. This milestone builds upon the FDA approval of TREMFYA ...
The FDA has approved Johnson & Johnson’s (J&J) Tremfya (guselkumab) for the treatment of moderately to severely active Crohn disease (CD). The regulatory action makes Tremfya the first and only ...
SPRING HOUSE, Pa. - Johnson & Johnson (NYSE: JNJ) has received Fast Track designation from the U.S. Food and Drug Administration (FDA) for nipocalimab, intended for the treatment of adult patients ...
Johnson & Johnson announced that the U.S. FDA has granted investigational nipocalimab Fast Track designation for the treatment of adult patients with moderate-to-severe Sjogren’s disease ...