Condition: Cholangiocarcinoma · Sponsor: Shanghai Zhongshan Hospital
This study is a prospective, observational study designed to analyze the safety, tolerability, and efficacy of first-line treatment using the combination of gemcitabine and cisplatin plus anti-PD-1/PD-L1 antibodies for patients with advanced cholangiocarcinoma.
This description comes directly from the study's public registry record.
Qinghai Ye, PhD · 2164041990 · 24111210117@m.fudan.edu.cn
Always discuss trial participation with your own doctor first.
| Zhongshan Hospital Fudan university | Shanghai, Shanghai Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07291063