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瑪仕度肽GLORY-1三期研究安全性-行業數據

瑪仕度肽GLORY-1三期研究安全性
瑪仕度肽GLORY-1三期研究安全性
瑪仕度肽耐受性和安全性良好?，斒硕入?4 mg 和 6 mg 組因不良事件導致研究藥物停用的受試者比例分別 1.5%和 0.5%，安慰劑組為 1.0%。胃腸道癥狀（惡心、腹瀉和嘔吐）是最常發生的不良事件，絕大多數為輕度或中度，且大部分發生于滴定期。
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瑪仕度肽GLORY-1三期研究安全性_第34頁
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瑪仕度肽GLORY-1三期研究安全性_第35頁
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瑪仕度肽GLORY-1三期研究安全性_第36頁
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瑪仕度肽GLORY-1三期研究安全性_第44頁
瑪仕度肽GLORY-1三期研究安全性_第45頁
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瑪仕度肽GLORY-1三期研究安全性_第47頁
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所屬報告： 信達生物-港股公司研究報告-非腫瘤領域即將迎來重磅商業化產品-250313（37頁）.pdf
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