Combination of 177Lu-TLX250 and Peposertib in Patients With Carbonic Anhydrase IX -Expressing Solid Tumors

PHASE1RecruitingINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

May 23, 2023

Primary Completion Date

December 31, 2024

Study Completion Date

December 31, 2026

Conditions
Solid Tumor, AdultAdvanced Solid TumorAdvanced Renal Cell Carcinoma
Interventions
DIAGNOSTIC_TEST

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

COMBINATION_PRODUCT

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."

Trial Locations (5)

Unknown

RECRUITING

Macquarie University, North Ryde

RECRUITING

Ashford (Icon) Cancer Centre, Adelaide

RECRUITING

Princess Alexandra Hospital, Brisbane

RECRUITING

Austin Health, Melbourne

RECRUITING

GenesisCare Murdoch, Perth

All Listed Sponsors
collaborator

Merck KGaA, Darmstadt, Germany

INDUSTRY

lead

Telix Pharmaceuticals (Innovations) Pty Limited

INDUSTRY