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Clinical Trial Summary

This is an open label, single arm, parallel-group, multicentre, and dose finding study to evaluate the safety of ascending radioactive dose levels of 131I-TLX101 administered intravenously in combination with best standard of care in newly diagnosed GBM patients.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05450744
Study type Interventional
Source Telix International Pty Ltd
Contact
Status Recruiting
Phase Phase 1
Start date April 1, 2023
Completion date June 2025

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