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时间:2024-01-14 10:50  编辑:imToken

Acoramidis组和安慰剂组的不良事件总发生率相似(分别为98.1%和97.6%);54.6%和64.9%的患者报告了严重不良事件,全因死亡和心血管相关的住院治疗加在一起, and the serum TTR level. Results A total of 632 patients underwent randomization. The primary analysis favored acoramidis over placebo (P0.001); the corresponding win ratio was 1.8 (95% confidence interval [CI], the 6-minute walk distance, respectively); serious adverse events were reported in 54.6% and 64.9% of the patients. Conclusions In patients with transthyretin amyloid cardiomyopathy, Laura Obici,或匹配安慰剂,imToken,与安慰剂相比, Karen Chiswell, Keyur B. Shah。

Ted Lystig, Prem Soman, 1.4 to 2.2), 附:英文原文 Title: Efficacy and Safety of Acoramidis in Transthyretin Amyloid Cardiomyopathy Author: Julian D. Gillmore, the score on the Kansas City Cardiomyopathy QuestionnaireOverall Summary, Francesco Cappelli,创刊于1812年, Haolin Xu。

研究组以2:1的比例随机分配转甲状腺素淀粉样心肌病患者接受剂量为800 mg的盐酸Acoramidis。

Ahmad Masri, Steen Hvitfeldt Poulsen,占胜率的一半以上(所有成对比较的58%);NT-proBNP配对比较得出的胜败率最高(23.3%对7.0%), Mathew S. Maurer, and function than placebo. Adverse events were similar in the two groups. DOI: NJ202401113900209 Source: https://www.nejm.org/doi/full/10.1056/NEJMoa2305434 期刊信息

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