Status:
RECRUITING
CAT-VHL Exploring the Role of Carbonic Anhydrase IX as Diagnostic and Theranostic Target in Von-Hippel Lindau Disease
Lead Sponsor:
IRCCS Ospedale San Raffaele
Conditions:
VHL - Von Hippel-Lindau Syndrome
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
The study is a phase 2, non-comparative and non-randomized, single arm, national clinical trial testing the hypothesis that CAIX-PET has diagnostic and theranostic potential in VHL disease and in VHL-...
Eligibility Criteria
Inclusion
- Voluntarily given informed consent
- Age ≥18 years old
- Performance Status ECOG/WHO score 0-2
- For females of reproductive potential, negative pregnancy test and use of highly effective contraception for 30 days following IMP administration
- For males of reproductive potential, use of highly effective contraception for 30 days following IMP administration.
- And, for the primary cohort:
- Diagnosis of VHL disease requiring surveillance following confirmation of pathogenic variant at genetic test
- Alternatively, for the secondary cohort:
- \- Clinical and/or pathological diagnosis of hemangioblastoma, pheochromocytoma, pancreatic neuroendocrine tumor or clear cell renal cell carcinoma requiring surgery.
Exclusion
- Performance Status ECOG/WHO score \>2
- Women who are pregnant or breastfeeding or are planning pregnancy during the study
- Men who are planning fatherhood during the study
- Exposure to any murine or chimeric antibodies within 5 years prior to the planned IMP administration
- Exposure to any experimental diagnostic or therapeutic drug within 30 days from the planned IMP administration
- Surgery, biopsy, ablative procedure, radiotherapy or any other local treatment for any primary tumor within 4 weeks prior to the planned IMP administration
- Exposure to any systemic agent within 4 weeks prior to the planned IMP administration or in case of continuing adverse effects with grade \>1 from such therapy
- Current exposure to systemic agents or scheduled therapy in the next 6 months following the planned IMP administration
- Serious non-malignant disease (e.g. psychiatric, infectious, autoimmune or metabolic) that may interfere with the objectives of the study or within the safety of compliance of the subjects as judged by the Investigator
- Known hypersensitivity to \[89Zr\]Zr-DFO-Girentuximab or DFO (Desferrioxamine)
- Severe chronic kidney disease with glomerular filtration rate ≤ 30 mL/min/1.73m2
- Other vulnerable categories than rare disease (e.g, being in detention)
Key Trial Info
Start Date :
January 23 2026
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 31 2026
Estimated Enrollment :
38 Patients enrolled
Trial Details
Trial ID
NCT07171905
Start Date
January 23 2026
End Date
December 31 2026
Last Update
December 5 2025
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
IRCCS Ospedale San Raffaele
Milan, Italia, Italy, 20132