Can sparsentan treat primary IgA nephropathy and its efficacy evaluation
In the international phase III clinical study (PROTECT trial) for the treatment of primary IgA nephropathy, sparsentan showed superior efficacy to conventional RAAS inhibitors. The results of the study showed that the urine protein/creatinine ratio of patients treated with sparsentan decreased by approximately 50% on average within 36 weeks, which was significantly higher than that of the irbesartan group (a decrease of approximately 15%-20%). In addition, patients' glomerular filtration rate (eGFR) declined more slowly, suggesting the drug's clinical value in delaying the progression of IgA nephropathy.
Sparsentan is currently approved in the United States for the treatment of IgA nephropathy and focal segmental glomerulosclerosis (FSGS), and is considered a new breakthrough in the treatment of IgA nephropathy. The drug can effectively reduce proteinuria and delay the progression of renal failure, providing a new treatment option for patients whose condition cannot be controlled by traditional drugs. With the subsequent accumulation of more real-world data, sparsentan is expected to be approved for marketing in China, bringing more precise and longer-lasting treatment options to patients with IgA nephropathy.
Reference: https://www.drugs.com/
[ 免责声明 ] 本页面内容来自公开渠道(如FDA官网、Drugs官网、原研药厂官网等),仅供持有医疗专业资质的人员用于医学药学研究参考,不构成任何治疗建议或药品推荐。所涉药品可能未在中国大陆获批上市,不适用于中国境内销售和使用。如需治疗,请咨询正规医疗机构。本站不提供药品销售或代购服务。
.jpeg)