Efficacy and Safety of Sevelamer Carbonate in Chinese Nondialysis Chronic Kidney Disease Patients with Hyperphosphatemia: A Randomized, Double-Blind, Parallel-Group Study

• Published in: Kidney diseases Vol. 9; no. 2; pp. 82 - 93
• Main Authors: Chen, Wei, Liu, Hua-Feng, Chen, Qin-Kai, Zhao, Ming-Hui, Chen, Xiao-Nong, Liu, Hong, Wan, Jian-Xin, Li, Shao-Mei, Chen, Meng-Hua, Dai, Chun, Shi, Hong-Bin, Wei, Jia-Li, Zhao, Hong-Wen, Wang, Li-Hua, Long, Gang, Lu, Wan-Hong, Tang, Ying, Yang, Jun-Wei, Cao, Li-Ying, Tang, Dong-Xing, Yang, Yu-Qiong, Yu, Xue-Qing
• Format: Journal Article
• Language: English
• Published: Basel, Switzerland S. Karger AG 01.04.2023; Karger Publishers
• Subjects: Carbonates; Care and treatment; Chronic kidney failure; Cinacalcet; Clinical trials; Low density lipoproteins; Medical research; Medicine, Experimental; Phosphates; Phosphorus imbalance; Research Article; Sevelamer carbonate; China; Hyperphosphatemia; Chronic kidney disease; Nondialysis; Phosphate binder; Sevelamer carbonate
• ISSN: 2296-9381; 2296-9357
• DOI: 10.1159/000527833

Introduction: Previous studies suggested that sevelamer carbonate is well tolerated with a favorable efficacy and safety profile in both dialysis and nondialysis patients in Europe; however, the efficacy remains controversial, and few studies have examined sevelamer carbonate therapy in other ethnic nondialysis CKD patients. This study assessed the efficacy and safety of sevelamer carbonate in Chinese nondialysis CKD patients with hyperphosphatemia. Methods: The multicenter, randomized, double-blind, parallel-group, placebo-controlled, and phase 3 clinical trial enrolled 202 Chinese nondialysis CKD patients with serum phosphorus ≥1.78 mmol/L. Patients were randomly assigned 1:1 to receive sevelamer carbonate (2.4–12 g per day) or placebo for 8 weeks. The primary outcome was the change in serum phosphorous between baseline and week 8. Results: Totally 482 Chinese patients were screened and 202 were randomized (sevelamer carbonate, n = 101; placebo, n = 101). The mean serum phosphorous decreased significantly in patients treated with sevelamer carbonate compared with placebo (−0.22 ± 0.47 vs. 0.05 ± 0.44 mmol/L, p < 0.0001). Significantly (p < 0.0001), decreases of serum total cholesterol, low-density lipoprotein cholesterol, and calcium-phosphorus (Ca × P) product levels from baseline to week 8 were shown in sevelamer carbonate group compared with placebo group. Serum intact parathyroid hormone was not significantly changed in the sevelamer carbonate group (p = 0.83). Patients in the sevelamer carbonate group experienced similar adverse events as the placebo group. Conclusion: Sevelamer carbonate is an effective and well-tolerated phosphate binder in advanced nondialysis CKD Chinese patients with hyperphosphatemia.