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A Study of Sirolimus (Albumin-Bound) in Combination With Different ADCs Treatment of Advanced Solid Tumors
Sponsor: CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
Summary
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).
Official title: A Phase Ib/II Clinical Trial on the Safety and Efficacy of Sirolimus (Albumin-bound) Combined With Different ADCs in Patients With Advanced Solid Tumors
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
444
Start Date
2025-11-13
Completion Date
2028-10-30
Last Updated
2025-11-28
Healthy Volunteers
No
Conditions
Interventions
sirolimus (albumin-bound)
intravenous infusion
DP303c
intravenous infusion
SYS6043
intravenous infusion
SYS6002
intravenous infusion
SYS6010
intravenous infusion
Locations (1)
Fudan University Shanghai Cancer Center
Shanghai, China