Optimizing Psoriasis Treatment: GUIDE Trial Outcomes on Guselkumab Dosing
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European Commission Approves Janssen’s TREMFYA®▼ (guselkumab), a First-in-Class Treatment for Active Psoriatic Arthritis (PsA)
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Johnson & Johnson: U.S. FDA approves TREMFYA (guselkumab) for the treatment of pediatric plaque psoriasis and active psoriatic arthritis, marking a first and only approval for an IL-23 inhibitor
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Johnson & Johnson seeks U.S. FDA approval for first pediatric indications for TREMFYA (guselkumab)
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Johnson & Johnson: TREMFYA (guselkumab) is first and only IL-23 inhibitor to demonstrate sustained clinical and endoscopic outcomes with a fully subcutaneous regimen through 48 weeks in ulcerative colitis
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Two mechanisms. One target.  Audrey Gibson, PA-C, simplifies how guselkumab addresses IL-23–driven inflammation in a way that’s easy to understand and clinically relevant. See it in action: https://bit.ly/Dual-Mechanism-of-Action-of-Guselkumab | Rhapp | Facebook
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