FDA Approves Roivant’s Lisraya (brepocitinib) as First Oral Drug for Dermatomyositis
The FDA approved Roivant’s Lisraya (brepocitinib), the first oral dual TYK2/JAK1 inhibitor, to treat dermatomyositis in adults.
ALL ABOUT DAILYZ HEALTH NEWS
ALL ABOUT DAILYZ HEALTH NEWS
The FDA approved Pluvicto with androgen receptor inhibitors for earlier-stage PSMA-positive metastatic hormone-sensitive prostate cancer, expanding patient eligibility.
Read MoreAlkem Laboratories and Major Pharmaceuticals recalled 299,520 dabigatran etexilate capsules nationwide due to FDA quality concerns.
Read MoreChipotle removed jalapeños from some Minnesota restaurants after a Salmonella Javiana outbreak sickened 110 people linked to the peppers.
Read MoreThe CDC is investigating over 7,400 suspected Cyclospora cases and a second outbreak cluster amid a record U.S. cyclosporiasis surge in 2026.
Read MoreMidwest Poultry Services recalled nearly 1.6 million dozen eggs from Texas farms due to potential Salmonella Enteritidis contamination risk.
Read MoreFourteen Americans returning from Congo were quarantined for four days at a New York military base due to Ebola outbreak precautions.
Read MoreViiV Healthcare presented Phase IIIb VOGUE trial data comparing two-drug Dovato to three-drug Biktarvy in treatment-naïve adults with HIV at AIDS 2026.
Read MoreThe CDC is investigating nearly 7,000 suspected cyclosporiasis cases across 34 states since May 2026, with 1,645 confirmed infections.
Read MoreThe FDA approved Leqembi Iqlik subcutaneous injections as a once-weekly starting dose for early Alzheimer’s disease treatment at home.
Read MoreMichigan reports over 3,000 cyclosporiasis cases linked to lettuce and salad greens in southeast counties as of July 13, 2026.
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