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Prospective Pilot Study Assessing Imaging Performance of 89Zirconium-labelled Girentuximab (89Zr-TLX250) PET-CT in Patients With HepatoCellular Carcinoma, Biliary Tract Carcers or Gastro-Entero-Pancreatic Neuroendocrine Neoplasms.

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Radiation
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Precision medicine represents a major goal in oncology. It has its underpinning in the identification of biomarkers with diagnostic, prognostic, or predictive values. Gastro-entero-pancreatic neuroendocrine neoplasia (GEP-NENs) are rare tumors, but their frequency is increasing. In this context, the tumor expression of carbonic anhydrase IX (CAIX), complemented by a restricted profile in normal tissues, provides an opportunity for therapeutic targeting and precision medicine. Indeed, radiolabeling the anti-CAIX monoclonal antibody girentuximab with Zirconium 89 has shown promise as a novel positron emission tomography (PET) tracer and labeling with 177 Lutetium promise as a therapeutic agent in clear cell renal cell carcinoma (ccRCC) in the context of a theranostic approach. The purpose of this study is to evaluate the use of 89Zr-labeled girentuximab (89Zr-TLX250) as a novel, carbonic anhydrase IX (CAIX) targeted PET/CT tracer for the imaging of Gastro-Entero-Pancreatic Neuroendocrine Neoplasms, Hepatocellular Carcinoma or IntraHepatic Cholangiocarcinoma.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Provided written informed consent.

• Patients aged ≥ 18 years.

• \- For basket 1 and 2: HCC or ICC histologically proven: newly diagnosed patients or patients with suspected refractory, residual, or recurrent disease.

• \- For basket 3: Progressive GEP-NENs with low or heterogeneous expression of SSTR2 or progressive pancreatic NENs which previously received at least two systemic treatments (excluding SSA) or pancreatic NENs with germline or somatic VHL mutation or G3 GEP-NENs .

• Presence of at least one morphological evaluable lesion according to RECIST 1.1 using contrast CT/MRI.

• Patients must have an ECOG (Eastern Cooperative Oncology Group) performance status of 0 to 2.

• For cirrhotic patients: Child-Pugh ≤ B7.

• Patient affiliated to or beneficiary of the National Health Service.

Locations
Other Locations
France
CHU de Nantes
RECRUITING
Nantes
AP-HP - Site de Beaujon
NOT_YET_RECRUITING
Paris
Contact Information
Primary
Clément BAILLY
clement.bailly@chu-nantes.fr
+33240084136
Backup
Astrid GARREAU
astrid.garreau@chu-nantes.fr
+33253482840
Time Frame
Start Date: 2025-11-04
Estimated Completion Date: 2027-08-04
Participants
Target number of participants: 60
Treatments
Experimental: 89Zr-TLX250
Patients will be injected with a single dose of 89Zr-TLX250.
Sponsors
Leads: Nantes University Hospital

This content was sourced from clinicaltrials.gov

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