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Johnson & Johnson : TREMFYA® (guselkumab) Provides Sustained Improvements Across All Minimal Disease Activity Domains for Adults Living with Active Psoriatic Arthritis in Phase 3b Trial

New Comprehensive Phase 3 Data Show First-in-Class TREMFYA® (guselkumab) Provided Durable Improvements in Measures of Psoriatic Arthritis (PsA) Disease Activity Through Two Years

New Phase 3 Data Show First-in-Class TREMFYA® (guselkumab) Achieved Complete Skin Clearance and Favorable Joint Efficacy in Adult Patients with Active Psoriatic Arthritis (PsA) Through Two Years

Share this article SPRING HOUSE, Pa., March 16, 2021 /PRNewswire/  The Janssen Pharmaceutical Companies of Johnson & Johnson today announced long-term data from the Phase 3 DISCOVER-2 a study showing that the skin clearance, joint symptom relief, and safety of TREMFYA ® (guselkumab) previously demonstrated through 24 weeks and one year (Week 52) in adults with active psoriatic arthritis (PsA) continued through two years (Week 112). 1,2 These findings also confirmed that the robust efficacy TREMFYA demonstrated in patients at Week 24 on physical function, physical aspects of health-related quality of life, and resolution of enthesitis b and dactylitis 1-8 In addition, the extent of radiographic progression d was studied through two years. These data will be presented virtually in abstract, poster, and video form during the Innovations in Dermatology: Virtual Spring Conference, March 16–20, 2021.

Biologic approved for plaque psoriasis shows efficacy in PsA patients

Biologic approved for plaque psoriasis shows efficacy in PsA patients Prof  Iain McInnes, the lead author of DISCOVER-2, discusses the latest findings of the phase-3 global trial to assess guselkumab in biologic-naïve patients with psoriatic arthritis. Peter Doyle reports Sustained improvements over 52 weeks were noted in biologic-naïve patients with psoriatic arthritis (PsA) who were given a monoclonal antibody against interleukin-23 normally used for the treatment of plaque psoriasis, a recent study is reporting. In 2017, guselkumab, a human monoclonal antibody specific to interleukin-23p19, was approved to treat adults with moderate-to-severe plaque psoriasis and who were candidates for systemic therapy or phototherapy.

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