This study adopts a multi-center, open-label, non-randomized trial design. It plans to enroll patients with Advanced solid tumor. Dose-escalation and PK-expansion studies will be carried out to evaluate the safety, tolerability, and preliminary efficacy of sirolimus (albumin-bound) in combination with Different ADCs (DP303c/SYS6043/SYS6002/SYS6010) in this patient population, and to confirm the recommended phase 2 dose (RP2D).
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
444
intravenous infusion
intravenous infusion
intravenous infusion
intravenous infusion
intravenous infusion
Fudan University Shanghai Cancer Center
Shanghai, China
RECRUITINGThe occurrence and frequency of adverse events (AE) and serious adverse events (SAE)
Time frame: Up to approximately 36 weeks after the first participant is enrolled
dose - limiting toxicities (DLT)
Time frame: Up to approximately 36 weeks after the first participant is enrolled
The recommended phase 2 dose
Time frame: Up to approximately 36 weeks after the first participant is enrolled
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