36
Participants
Start Date
May 23, 2023
Primary Completion Date
December 31, 2024
Study Completion Date
December 31, 2026
89Zr-TLX250
Single IV administration followed by 89Zr-DFO-girentuximab PET/CT (or PET/MRI) scan at screening and approximately 8-10 weeks (±1 week) after Cycle 3 Day 1, as well as at the end of treatment visit (if feasible). The PET/CT should be obtained within 4-7 days after 89Zr-TLX250 administration
177Lu-TLX250 and Peposertib
"Dose escalation and de-escalation for the determination of the Maximum tolerated combination/ Recommended phase 2 dose.~All subjects will receive 177Lu-TLX250 intravenously on day 1 and Peposertib BID on days 4-21 of each 84-day cycle."
RECRUITING
Macquarie University, North Ryde
RECRUITING
Ashford (Icon) Cancer Centre, Adelaide
RECRUITING
Princess Alexandra Hospital, Brisbane
RECRUITING
Austin Health, Melbourne
RECRUITING
GenesisCare Murdoch, Perth
Merck KGaA, Darmstadt, Germany
INDUSTRY
Telix Pharmaceuticals (Innovations) Pty Limited
INDUSTRY