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A Study of ASP1951 in Subjects With Advanced Solid Tumors

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NIAID Data Ecosystem2026-03-10 收录
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https://www.omicsdi.org/dataset/ecrin-mdr-crc/2293965
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资源简介:
The primary purpose of this study is to evaluate the tolerability and safety profile of ASP1951 when administered as a single agent and in combination with pembrolizumab in participants with locally advanced (unresectable) or metastatic solid tumors; characterize the pharmacokinetic profile of ASP1951 when administered as a single agent and in combination with pembrolizumab; and determine the recommended phase 2 dose (RP2D) of ASP1951 and/or maximum tolerated dose (MTD) when administered as a single agent and in combination with pembrolizumab. This study will also evaluate the anti-tumor effect of ASP1951 when administered as a single agent and in combination with pembrolizumab.
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2019-01-15
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