CAIX PET/CT for Residual or Recurrent Post-ablative ccRCC

Part of paid clinical trials in Boston, Massachusetts.

Sponsor
Massachusetts General Hospital
Study ID
NCT07077083
Phase
PHASE2
Status
Not Yet Recruiting

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Conditions

  • Clear Cell Renal Cell Carcinoma (ccRCC)
  • ccRCC

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • 89Zr-Girentuximab — DRUG
    89Zr-Girentuximab PET

Study Details

The goal of this clinical trial is to learn whether 89Zr-Girentuximab PET scans can inform management of renal cell carcinoma. The main questions it aims to answer are: * Does the 89Zr-Girentuximab PET detect ccRCC that is left behind or has come back after treatment? * What differences can be seen on the 89Zr-Girentuximab PET before and after standard of care treatment? Participants in arm 1 will be given the study drug followed by a PET scan 3-7 days after injection. Participants in arm 2 will receive the same, but will proceed with their standard of care cryoablation after the initial PET scan. Within 3 days of the cryoablation treatment, participants will receive a repeat PET scan.

Key Dates

Start date
Mar 16, 2026
Status verified
Jul 2025
Primary completion
Aug 1, 2027
Completion
Aug 1, 2028

Study Design

Enrollment
10 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC

Arms

  • Experimental: Patients with known or suspected recurrent or residual ccRCC
    PET and Histological correlation
  • Experimental: Patients with ccRCC undergoing ablation
    PET for evaluation of post-ablative kidney

Primary Outcome Measure

SUVmean of the ablated zone and adjacent or contralateral uninvolved kidney [ Time Frame: From enrollment to 0-3 days after SOC cryoablation ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Massachusetts General HospitalBostonMassachusetts02114
Taylor McVeigh
6177261312
Shadi Abdar Esfahani, MD, MPH (PRINCIPAL_INVESTIGATOR)

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