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Supplementary Material for: Enarodustat for the Treatment of Anemia in Chinese Patients with Non-Dialysis Chronic Kidney Disease: A Phase 3 Trial

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Figshare2024-12-20 更新2026-04-28 收录
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https://figshare.com/articles/dataset/Supplementary_Material_for_Enarodustat_for_the_Treatment_of_Anemia_in_Chinese_Patients_with_Non-Dialysis_Chronic_Kidney_Disease_A_Phase_3_Trial/28070855
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Introduction: Renal anemia is a common complication among patients with non-dialysis chronic kidney disease (ND-CKD), and there remains an unmet need for more efficient and convenient daily oral medications to improve patient outcomes. This study aimed to evaluate the efficacy and safety of enarodustat, a hypoxia-inducible factor prolyl hydroxylase inhibitor, in treating anemia for ND-CKD patients. Methods: This phase 3 study was conducted at 48 centers across China, enrolling 156 ND-CKD patients. Participants were randomly randomized in a 2:1 ratio to receive either enarodustat or placebo for an initial 8-week double-blind period, followed by a 16-week open-label period during which all patients received enarodustat. Results: The primary endpoint was the mean change in hemoglobin (Hb) levels from baseline to the average level during weeks 7-9. Secondary endpoints focused on Hb concentration or treatment pattern, while exploratory endpoints assessed iron metabolism-related parameters. The mean (±SD) change in Hb levels from baseline to weeks 7-9 was 15.99 (±9.46) g/L in the enarodustat group, compared to -0.14 (±8.08) g/L in the placebo group, resulting in a mean difference of 16.00 (±1.54) g/L (P<0.001). During weeks 7-9, 85.3% of patients in the enarodustat group achieved Hb levels ≥ 100 g/L. with 86.0% maintaining this level during weeks 21-25. In the first 4 weeks, the Hb increased by 11.82 (± 9.56) g/L in the enarodustat group. By week 9, the mean change in hepcidin level was -42.94(± 37.56) ng/mL in the enarodustat group, compared to +4.58(±33.34) ng/mL in the placebo group. Enarodustat also improved other iron-related parameters and reduced the need for iron supplements. The safety profile of enarodustat was well-tolerable with adverse events comparable to those of the placebo. Conclusion: Enarodustat effectively corrected renal anemia with a manageable safety profile. Its once-daily oral administration offers convenience that may enhance the adherence. Enarodustat shows the potential as a promising therapy for anemic patients with ND-CKD.
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2024-12-20
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