Johnson & Johnson Reports Phase 3 subgroup analysis Data for Vadadustat in Multiple myeloma

Johnson & Johnson today announced Phase 3 subgroup analysis results for Vadadustat in patients with Multiple myeloma. The study demonstrated that Vadadustat demonstrates durable complete remissions compared to standard of care or placebo. These results provide important insights into the treatment of Multiple myeloma and support the continued development of Vadadustat in this patient population. The data were presented at a major medical conference and will be submitted for publication in a peer-reviewed journal. Regulatory submissions are planned based on these results. The safety profile of Vadadustat was consistent with previous observations, with no new safety signals identified.