89Zr-TLX250 for PET/CT Imaging of ccRCC- ZIRCON Study
NCT03849118 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 300
Last updated 2024-05-17
Summary
89Zr-TLX250 is under clinical development as a diagnostic agent targeting clear cell renal cell carcinoma.
Conditions
Interventions
- DIAGNOSTIC_TEST
-
89Zr-girentuximab
Single IV administration on Day 0, followed by diagnostic scan on Day 5 +/- 2 days.
Sponsors & Collaborators
-
Telix Pharmaceuticals (Innovations) Pty Limited
lead INDUSTRY
Principal Investigators
-
Howard Gurney, MD · Macquarie University Hospital
-
Francoise Brodere, MD · University Hospital ICO, Nantes, France
-
Peter Mulders, MD · Radboud University Medical Center
-
Marcel Stokkel, MD · The Netherlands Cancer Institute
-
Declan Murphy, MD · Victorian Comprehensive Cancer Centre
-
Andrew Scott, MD · Olivia Newton John Cancer Research Center, Austin Hospital
-
Simon Wood, MD · Princess Alexander Hospital
-
Mark Frydenberg, MD · Cabrini Hospital
-
David Chan · Royal North Shore Hospital
-
Jean-Christophe Bernhard, MD · CHU de Bordeaux, Groupe Hospitalier Pellegrin
-
Pierre Olivier, MD · CHRU de Nancy - Hôpitaux de Brabois
-
Linda Heijmen, MD · Leiden University Medical Centre
-
Martin Geert Steffens, MD · Isala
-
Karolien Goffin, MD · Universitair Ziekenhuis Leuven
-
Carlos Artigas Guix, MD · Instutit Jules Bordet
-
Nicolas Lumen, MD · University Ghent
-
Sumer Baltaci, MD · Ankara University
-
Bulent Akdogan, MD · Ankara Hacettepe University
-
Bulent Onal, MD · Istanbul University - Cerrahpasa
-
Tamer Aksoy, MD · Istanbul Training and Research Hospital
Study Design
- Allocation
- NA
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-08-15
- Primary Completion
- 2022-10-20
- Completion
- 2022-11-07
- FDA Drug
- Yes
Countries
- United States
- Australia
- Belgium
- Canada
- France
- Netherlands
- Turkey (Türkiye)
- United Kingdom
Study Locations
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