Finding studies
Finding studies
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Clinical Trials Information Group officer
CONTACT
Xiaohua Wu
CONTACT
Lead
CSPC Megalith Biopharmaceutical Co.,Ltd.
The study aims to evaluate the safety/tolerability, pharmacokinetics, and preliminary efficacy of SYS6041 in combination with other agents in subjects with recurrent ovarian cancer. Eligible subjects will receive SYS6041 in combination with different agents (carboplatin, paclitaxel, bevacizumab, enlonstobart) . Each treatment cycle lasting 3 weeks, until disease progression, intolerable toxicity, initiation of new anti-tumor therapy, withdrawal of informed consent, loss to follow-up, or death, whichever occurs first.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted