Study of 111In-XYIMSR-01 SPECT/CT in Patients With Metastatic Clear Cell Renal Cell

Recruiting now · Phase 1

Conditions studied: Renal Cell Carcinoma (Kidney Cancer)

In brief

This study is being done to determine if the investigational radiotracer called 111In-XYIMSR-01 is helpful in detecting clear cell renal cell carcinoma tissue in your body when used during a SPECT-CT Scan

Key facts

Study ID

NCT07062549

Run by

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

People needed

6

Starts

2022-01-26

Expected to finish

2029-07-01

Last updated by the study team

2026-07-21

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Males or female sex
• ≥18 years of age
• Willingness to provide signed informed consent and comply with all protocol requirements
• Histological confirmation of RCC with a clear cell component
• 2-10 sites of disease measuring ≥1.5 cm on contrast-enhanced CT and/or MRI imaging of the chest, abdomen and pelvis performed ≤60 days prior to the date of study enrollment
• Screening clinical laboratory values as specified below:
• Serum bilirubin ≤ 1.5 times the upper limit of normal; for patients with known Gilbert's syndrome, ≤ 3 × ULN is permitted
• ALT ≤ 3 times the upper limits of normal
• AST ≤ 3 times the upper limits of normal
• Creatinine clearance ≥50 mL/min based on Cockcroft-Gault formula
• Absolute neutrophil count ≥ 1,500 /mm3
• Platelets ≥100,000/ mm3
• Hemoglobin ≥ 9.0 g/dL
• White blood cell count ≥ 2,000/ mm3

You may not qualify if…

• Systemic therapy for the treatment of ccRCC within 12 months of study enrollment.
• Subjects administered any radioisotope within five physical half-lives prior to study drug injection.
• Subjects with any medical condition or other circumstances that, in the opinion of the investigator, compromise obtaining reliable data, achieving study objectives, or completion.
• Women of child-bearing potential (WOCBP) must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of human chorionic gonadotropin) within 24 hours prior to the imaging day.
• Women must not be breastfeeding.

Where it is running

• Johns Hopkins University — Baltimore, Maryland, United States (enrolling)

Full record on ClinicalTrials.gov

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