4.6 Article

Efficacy and safety of vadadustat compared with darbepoetin alfa in Japanese anemic patients on hemodialysis: a Phase 3, multicenter, randomized, double-blind study

Journal

NEPHROLOGY DIALYSIS TRANSPLANTATION
Volume 36, Issue 9, Pages 1731-1741

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ndt/gfab055

Keywords

anemia; chronic kidney disease; hemodialysis; hypoxia-inducible factor prolyl hydroxylase inhibitor; vadadustat

Funding

  1. Mitsubishi Tanabe Pharma Corporation

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The study compared the efficacy and safety of vadadustat with darbepoetin alfa in Japanese anemic patients on hemodialysis. Vadadustat was found to be noninferior to darbepoetin alfa in maintaining hemoglobin levels within the target range, with similar adverse events observed in both groups. This suggests that vadadustat can be a viable alternative to ESA in managing anemia in Japanese hemodialysis patients.
Background Vadadustat is an oral hypoxia-inducible factor prolyl hydroxylase inhibitor that stimulates erythropoiesis. Methods The efficacy and safety of vadadustat, compared with darbepoetin alfa, was determined in a Phase 3 double-blind study in Japanese anemic patients on hemodialysis. Patients receiving erythropoiesis-stimulating agents (ESAs) were randomized and switched to either vadadustat or darbepoetin alfa for 52 weeks. Doses were adjusted to maintain a hemoglobin (Hb) level of 10.0-12.0g/dL. The primary endpoint was average Hb level at Weeks 20 and 24. Results Of the 323 randomized patients, 120 and 135 completed the 52-week treatment period in the vadadustat and darbepoetin alfa groups, respectively. The average Hb levels at Weeks 20 and 24 [least square mean (LSM) and 95% confidence interval (CI)] were 10.61 (10.45-10.76) and 10.65 (10.50-10.80) g/dL in the vadadustat and darbepoetin alfa groups, respectively, demonstrating vadadustat's noninferiority to darbepoetin alfa (difference: -0.05g/dL; 95% CI -0.26 to 0.17). In both groups, the mean Hb levels were maintained within the target range for 52weeks. Furthermore, irrespective of patient backgrounds, the LSMs of Hb at Week 52 were within the target range. The most common adverse events were nasopharyngitis, diarrhea and shunt stenosis, which occurred at similar frequencies in both groups. No new safety concerns were identified. Conclusions Vadadustat was as well-tolerated and effective as darbepoetin alfa in maintaining Hb levels within the target range. The findings suggest that vadadustat can be an alternative to ESA in the management of anemia in Japanese hemodialysis patients receiving ESA.

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