Finding studies
Finding studies
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Lead
Chugai Pharmaceutical
This is a Phase I open-label dose escalation study of GC33 in patients with advanced or metastatic HCC. This study is designed to evaluate safety, tolerability, pharmacokinetics, and preliminary assessment of anti-tumor activity. Enrollment will proceed until a maximum tolerated dose (MTD) and a recommended Phase II dose has been established.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted