drugset / Trial / NCT07608848

First-in-human Diagnostic Imaging Profile of the Theranostic Pair [68Ga]Ga-DOTA-STR-17126 and Low Dose [177Lu] Lu-DOTA-STR-17126 in Patients With Advanced or Metastatic Cancer

NCT07608848 ↗

Phase 0 Recruiting 20 enrolled Integrated Haematology and Oncology Network
NaSingle-groupOpen-labelDiagnostic

Summary

This is an open-label, first-in-human, exploratory Phase 0 study evaluating the safety and diagnostic imaging performance of the DOTA-STR-17126 theranostic pair in patients with advanced or metastatic breast or prostate cancer. The study investigates \[68Ga\]Ga-DOTA-STR-17126 for PET imaging and, in patients with positive GRPR uptake, a low dose of \[177Lu\]Lu-DOTA-STR-17126 for SPECT imaging and dosimetry. The primary objective is to assess safety and tolerability. Secondary objectives include evaluation of imaging quality, biodistribution, pharmacokinetics, and radiation dosimetry. Exploratory objectives assess correlations between GRPR expression in tumour tissue and imaging uptake. The study is conducted at a single centre in Australia, with 12 evaluable participants (up to 20 enrolled), and supports the development of a GRPR-targeted theranostic approach for personalised cancer management.

Timeline

Start
2026-05-28
Primary completion
2028-05-30
Completion
2029-05-31

Drugs

EvaluationDrugModalityDoseRoute
Subject [177Lu]Lu-DOTA-STR-17126 Diagnostic / imaging agent 50 ug Intravenous
Subject [177Lu]Lu-DOTA-STR-17126 Diagnostic / imaging agent 1000 mbq Intravenous
Subject [68Ga]Ga-DOTA-STR-17126 Diagnostic / imaging agent 50 ug Intravenous
Subject [68Ga]Ga-DOTA-STR-17126 Diagnostic / imaging agent 150 mbq Intravenous