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RECRUITING
NCT07241936
PHASE1/PHASE2

A Study of Sirolimus (Albumin-Bound) in Combination With Different ADCs Treatment of Advanced Solid Tumors

Sponsor: CSPC ZhongQi Pharmaceutical Technology Co., Ltd.

View on ClinicalTrials.gov

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

Interventions

DRUG

sirolimus (albumin-bound)

intravenous infusion

DRUG

DP303c

intravenous infusion

DRUG

SYS6043

intravenous infusion

DRUG

SYS6002

intravenous infusion

DRUG

SYS6010

intravenous infusion

Locations (1)

Fudan University Shanghai Cancer Center

Shanghai, China