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Clinical Trial Summary

This is a single arm, open label, multi-center phase I study, including phase Ia dose escalation and phase Ib dose expansion. Safety review committee (SRC) will be formed to monitor safety and efficacy data through the study. And the independent review committee (IRC) will be formed to monitor efficacy data through the study.


Clinical Trial Description

The efficacy and safety of Yttrium-90 carbon microspheres in patients with unresectable LAPC remain unknown. This trial is a prospective, multicenter, open-label, single-arm phase I trial designed to evaluate the safety and efficacy of NRT6008 injection. The primary objective is to evaluate the safety of NRT6008 Injection. While the secondary objectives include the assessments of the preliminary efficacy. In addition, the distribution of NRT6008 injection in human body, and the changes of tumor biomarkers and the improvement of cancer pain status of participants after administration will also be evaluated. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06278454
Study type Interventional
Source Chengdu New Radiomedicine Technology Co. LTD.
Contact Zhaoshen Li
Phone +8602131162338
Email zhsl@vip.163.com
Status Not yet recruiting
Phase Phase 1
Start date March 2024
Completion date December 2026

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