Enarodustat for the Treatment of Anemia in Chinese Patients with Non-Dialysis Chronic Kidney Disease: A Phase 3 Trial
Year: 2024
Type: article
Study designs: Randomized Controlled Trial, Clinical Trial
Abstract: 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.
Source: Kidney Diseases
DOI: 10.1159/000543193
Authors: Xin-Ling Liang, Ren-Wei Huang, Jian-Teng Xie, Yan-Ning Zhang, Yi-Nan Li, Xiao-Nong Chen, Tian-Jun Guan, Hua Zhou, Ping Fu, Yun-Hua Liao, Hui Xu, Ai-Cheng Yang, Hong-Wen Zhao, Zi-Chen Liu, Li-Li Yang, Xue-Qing Yu
Institutions: Guangdong Academy of Medical Sciences, Guangdong Provincial People's Hospital, Southern Medical University, General Hospital of Shenyang Military Region, First Affiliated Hospital of Xiamen University, Shanghai Jiao Tong University, Ruijin Hospital, Xiamen University, Zhongshan Hospital of Xiamen University, Sheng Jing Hospital, China Medical University, Sichuan University, West China Hospital of Sichuan University, Guangxi Medical University, First Affiliated Hospital of GuangXi Medical University, Central South University, Xiangya Hospital Central South University, Jiangmen Wuyi Traditional Chinese Medicine Hospital, Army Medical University
Language: English
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,320
OpenAlex ID: W4405621681
