drugset / Trial / NCT07259889

Safety and Tolerability Evaluation of CEL001 Injection in Advanced Solid Tumors

NCT07259889 ↗

Phase 1 Recruiting 13 enrolled Guangzhou Xiling Biotechnology Co., Ltd.
Non-randomizedSequentialOpen-labelTreatment

Summary

This study is the first human, open label, dose escalation, and expansion phase I clinical trial aimed at evaluating the safety, tolerability, preliminary efficacy, pharmacokinetic characteristics, biomarker changes, and immunogenicity of CEL001 injection in the treatment of advanced solid tumors.

Timeline

Start
2025-06-16
Primary completion
2028-06-15
Completion
2028-06-15

Drugs

EvaluationDrugModalityDoseRoute
Subject CEL001 Cell therapy 5e+08 cells Intravenous
Subject CEL001 Cell therapy 2e+09 cells Intravenous
Subject CEL001 Cell therapy 5e+09 cells Intravenous

Indications

No indication recorded.