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Clinical Trial Summary

The purpose of this long-term safety study is to follow up subjects treated with CTX0E03 DP to monitor for delayed oncological, neurological, and CTX0E03 DP-related adverse events and to monitor survival


Clinical Trial Description

The goal of this study is to assess the long-term safety of subjects treated with intracerebral CTX0E03 DP as measured by the onset of delayed adverse events of special interest (AESIs). AESIs are defined as adverse events leading to death, new oncological adverse events, new neurological adverse events and any other adverse event, which in the opinion of the Safety/Project Physician is related to CTX0E03 DP. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05598775
Study type Observational
Source ReNeuron Limited
Contact
Status Enrolling by invitation
Phase
Start date November 1, 2022
Completion date December 31, 2026

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