J&J Wins First FDA Approval for Warm Autoimmune Hemolytic Anemia
Johnson & Johnson received the first FDA approval for Imaavy, a treatment targeting warm autoimmune hemolytic anemia. In 115 adults, patients on Imaavy were about three times as likely as placebo to achieve sustained hemoglobin improvement after 24 weeks, according to trial results. Shares fell about 1%, as investors focused on the commercial ramp despite strong sales and increased revenue guidance.