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

Recruiting Phase 1 Phase 2 Interventional Study
Advanced Solid Tumors
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 75
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Treatment
Participants needed
444 (estimated)
Sponsor
CSPC ZhongQi Pharmaceutical Technology Co., Ltd. · Industry
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About This Trial
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 re…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 1\. Subjects aged 18 to 75 years (inclusive). * 2\. Patients with advanced solid tumors that are unresectable or metastatic and confirmed by histology or cytology. * 3\. At least one measurable lesion, as defined by RECIST 1.1 criteria. * 4\. ECOG performance status of 0 or 1.…
Contacts

Clinical Trials Information Group officer

86-0311-69085587

ctr-contact@cspc.cn

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