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HLX10-015-CRC301臨床試驗結果（截至2024H1）-行業數據

HLX10-015-CRC301臨床試驗結果（截至2024H1）
HLX10-015-CRC301臨床試驗結果（截至2024H1）
安全性方面：大多數 irAEs為輕度（1-2 級）；A組中 12.7%的患者發生了≥3 級的 irAEs；B組中有 1.8%的患者發生了≥3 級的 irAEs。
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第1頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第2頁
HLX10-015-CRC301臨床試驗結果（截至2024H1）_第3頁
HLX10-015-CRC301臨床試驗結果（截至2024H1）_第4頁
HLX10-015-CRC301臨床試驗結果（截至2024H1）_第5頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第6頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第7頁
HLX10-015-CRC301臨床試驗結果（截至2024H1）_第8頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第9頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第10頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第11頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第12頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第13頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第14頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第15頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第16頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第17頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第18頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第19頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第20頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第21頁
HLX10-015-CRC301臨床試驗結果（截至2024H1）_第22頁
HLX10-015-CRC301臨床試驗結果（截至2024H1）_第23頁
HLX10-015-CRC301臨床試驗結果（截至2024H1）_第24頁
HLX10-015-CRC301臨床試驗結果（截至2024H1）_第25頁
HLX10-015-CRC301臨床試驗結果（截至2024H1）_第26頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第27頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第28頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第29頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第30頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第31頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第32頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第33頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第34頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第35頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第36頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第37頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第38頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第39頁
HLX10-015-CRC301臨床試驗結果（截至2024H1）_第40頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第41頁
HLX10-015-CRC301臨床試驗結果（截至2024H1）_第42頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第43頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第44頁
HLX10-015-CRC301臨床試驗結果（截至2024H1）_第45頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第46頁
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HLX10-015-CRC301臨床試驗結果（截至2024H1）_第47頁
所屬報告： 復宏漢霖-港股公司研究報告-再啟航創新+國際化步入收獲期-250427（46頁）.pdf
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