Condition: Advanced Solid Tumor · Sponsor: Hansoh BioMedical R&D Company
This is a Phase I clinical study of HS-20108. The purpose of this study is to evaluate the safety, tolerability, PK and efficacy of intravenous HS-20108 in patients with advanced solid tumors.
This description comes directly from the study's public registry record.
Jie Chen, Doctor · +8613660217442 · Chen0jie@hotmail.com
Always discuss trial participation with your own doctor first.
| Fudan University Shanghai Cancer Center | Shanghai, Shanghai Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06936735