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Efficacy, tolerability, and safety of the oral phosphate binder VS-505 (AP301).
Zhuang, Bing; Gan, Liangying; Liu, Bin; Yuan, Weijie; Shi, Ming; Peng, Ai; Wang, Lihua; Chen, Xiaolan; Liu, Tongqiang; Zhang, Shiying; Wang, Song; Gao, Qing; Wang, Baoxing; Zheng, Huixiao; Liu, Changhua; Luo, Yuan; Ye, Hong; Lin, Hongli; Li, Yiwen; He, Qiang; Zheng, Feng; Luo, Ping; Long, Gang; Lu, Wei; Li, Kanghui; Yang, Junwei; Liu, Yingxue Cathy; Zhang, Zhizheng; Li, Xiaolin; Zhang, Weifeng; Zuo, Li.
Afiliação
  • Zhuang B; Center for Kidney Disease, Second Affiliated Hospital, Nanjing Medical University, Nanjing, China.
  • Gan L; Department of Nephrology, Peking University People's Hospital, Beijing, China.
  • Liu B; Nephrology Department, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, China.
  • Yuan W; Nephrology Department, Shanghai General Hospital, Shanghai, China.
  • Shi M; Nephrology Department, Renmin Hospital of Wuhan University, Wuhan, China.
  • Peng A; Nephrology Department, Shanghai Tenth Hospital, Shanghai, China.
  • Wang L; Nephrology Department, The Second Hospital of Shanxi Medical University, Taiyuan, China.
  • Chen X; Nephrology Department, Affiliated Hospital of Nantong University, Nantong, China.
  • Liu T; Nephrology Department, Changzhou No. 2 People's Hospital, Changzhou, China.
  • Zhang S; Nephrology Department Jilin Province People's Hospital, Changchun, China.
  • Wang S; Nephrology Department, Peking University Third Hospital, Beijing, China.
  • Gao Q; Department of Nephrology, Zhongshan Hospital of Xiamen University School of Medicine, Xiamen, China.
  • Wang B; Nephrology Department, The Third Hospital of Hebei Medical University, Shijiazhuang, China.
  • Zheng H; Nephrology Department, The Second Affiliated Hospital of Xingtai Medical College, Xingtai, China.
  • Liu C; Nephrology Department, Northern Jiangsu People's Hospital, Yangzhou, China.
  • Luo Y; Center for Kidney Disease, Second Affiliated Hospital, Nanjing Medical University, Nanjing, China.
  • Ye H; Center for Kidney Disease, Second Affiliated Hospital, Nanjing Medical University, Nanjing, China.
  • Lin H; Nephrology Department, The First Hospital of Dalian Medical University, Dalian, China.
  • Li Y; Department of Nephrology, Zhejiang Provincial People's Hospital, Hangzhou, China.
  • He Q; Department of Nephrology, Zhejiang Provincial People's Hospital, Hangzhou, China.
  • Zheng F; Nephrology Department, The Second Hospital of Dalian Medical University, Dalian, China.
  • Luo P; Nephrology Department, The Second Hospital of Jilin University, Changchun, China.
  • Long G; Department of Nephrology, Tianjin Union Medical Center, Tianjin, China.
  • Lu W; Department of Nephrology, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
  • Li K; Nephrology Department, The Affiliated Hospital of Guilin Medical University, Guilin, China.
  • Yang J; Center for Kidney Disease, Second Affiliated Hospital, Nanjing Medical University, Nanjing, China.
  • Liu YC; Shanghai Alebund Pharmaceuticals Limited, Shanghai, China.
  • Zhang Z; Shanghai Alebund Pharmaceuticals Limited, Shanghai, China.
  • Li X; Shanghai Alebund Pharmaceuticals Limited, Shanghai, China.
  • Zhang W; Shanghai Alebund Pharmaceuticals Limited, Shanghai, China.
  • Zuo L; Department of Nephrology, Peking University People's Hospital, Beijing, China.
Article em En | MEDLINE | ID: mdl-38453435
ABSTRACT

BACKGROUND:

VS-505 (AP301), an acacia and ferric oxyhydroxide polymer, is a novel fiber-iron-based phosphate binder. This two-part phase 2 study evaluated the tolerability, safety, and efficacy of oral VS-505 administered three times daily with meals in treating hyperphosphatemia in chronic kidney disease (CKD) patients receiving maintenance hemodialysis (MHD).

METHODS:

In Part 1, patients received dose-escalated treatment with VS-505 2.25, 4.50, and 9.00 g/day for 2 weeks each, guided by serum phosphorus levels. In Part 2, patients received randomized, open-label, fixed-dosage treatment with VS-505 (1.50, 2.25, 4.50, or 6.75 g/day) or sevelamer carbonate 4.80 g/day for 6 weeks. The primary efficacy endpoint was the change in serum phosphorus.

RESULTS:

The study enrolled 158 patients (Part 1 25; Part 2 133), with 130 exposed to VS-505 in total. VS-505 was well tolerated. The most common adverse events were gastrointestinal disorders, mainly feces discolored (56%) and diarrhea (15%; generally during weeks 1‒2 of treatment). Most gastrointestinal disorders resolved without intervention, and none were serious. In Part 1, serum phosphorus significantly improved (mean change -2.0 mg/dL; 95% confidence interval -2.7, -1.4) after VS-505 dose escalation. In Part 2, serum phosphorus significantly and dose-dependently improved in all VS-505 arms, with clinically meaningful reductions with VS-505 4.50 and 6.75 g/day, and sevelamer carbonate 4.80 g/day (mean change -1.6 (-2.2, -1.0), -1.8 (-2.4, -1.2), and -1.4 (-2.2, -0.5) mg/dL, respectively). In both Parts, serum phosphorus reductions occurred within 1 week of VS-505 initiation, returning to baseline within 2 weeks of VS-505 discontinuation.

CONCLUSION:

VS-505, a novel phosphate binder, was well tolerated with a manageable safety profile, and effectively and dose-dependently reduced serum phosphorus in CKD patients with hyperphosphatemia receiving MHD. Clinical Trial registration number NCT04551300.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article