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TREMFYA® is now approved for pediatric patients living with moderate to severe plaque psoriasis, who are candidates for systemic therapy or phototherapy, and active psoriatic arthritis in children six years and older, weighing at least 40 kg Approval was based on PROTOSTAR study, which showed pediatric patients receiving TREMFYA® achieved high levels of skin clearance vs. placebo at Week 16

Her natural curiosity, determination and fascination with science inspired Esi Lamousé, M.D., Ph.D., to pursue a career that’s helped bring innovative therapies for inflammatory bowel disease to patients in need around the world.

Investment brings total J&J Foundation commitment to $20 million to support deployment of 200,000 professional community health workers to bring more communities closer to care Announced during a UN General Assembly side event focused on strengthening health systems and tackling health threats

Through collaborations with Americares, Heart to Heart International and the American Red Cross, Johnson & Johnson, with support from the J&J Foundation is standing with those who care for communities when catastrophe occurs.

Seltorexant, in combination with an oral antidepressant, demonstrated a numerically greater response rate at week 26 with a more favorable safety and tolerability profile compared to adjunctive quetiapine XR Patients treated with adjunctive seltorexant also saw notably less weight gain, and somnolence rates were four times lower than those in patients treated with adjunctive quetiapine XR

TREMFYA® offers the flexibility of self-administration from the start of treatment, building on the prior approval of subcutaneous induction in Crohn’s disease TREMFYA® achieved significant rates of clinical remission and endoscopic improvement versus placebo at Week 12 with a subcutaneous induction regimen, consistent with IV induction Johnson & Johnson is initiating a head-to-head study seeking to demonstrate the superiority of TREMFYA® vs. Skyrizi® (risankizumab) in Crohn’s disease, based on the confidence in the clinical profile

Across three days, a group of New Jersey high school students participated in a broad range of STEM-focused activities, workshops, speaker sessions and a site tour as part of Johnson & Johnson’s WiSTEM²D Camp global initiative.

Pending the European Commission’s final decision, nipocalimab could be the first FcRn blocker approved in both adult and adolescent gMG patients aged 12 and older who are anti-AChR or anti-MuSK antibody-positive CHMP opinion is supported by results from the Phase 3 Vivacity-MG3 and Phase 2/3 Vibrance-mg studies over 24 weeks, which demonstrated a sustained reduction in immunoglobulin G (IgG) levels, one of the root causes of autoantibody diseases

100 percent of evaluable patients achieved minimal residual disease (MRD) negativity Updated Phase 2 MajesTEC-5 results underscore the importance of additional treatment options earlier in the disease