
The abstract is for reference only. Please refer to the full text of the announcement on the very day.
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Filed with SSE · Stock code 688578 · · 3 pages · Chinese
The trial, known as FURVENT, did not meet its primary endpoint of progression-free survival as assessed by independent review. However, clinical benefits were observed in secondary endpoints, and safety data were consistent with previous studies. The company is evaluating the complete dataset to determine future steps regarding the drug's development.
Written in English by 6ix AI from the company’s Chinese-language filing. How 6ix writes summaries

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