Purpose

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

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • 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

Exclusion Criteria

  • 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.

Study Design

Phase
Phase 1
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Primary Purpose
Other
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
A (111In-XYIMSR-01)
Participants who receive 111In-XYIMSR-01 dosing and SPECT/CT imaging
  • Drug: 111In-XYIMSR-01
    Unite Dose: 10.5±1 mCi of 111In-XYIMSR-01 Route of administration: Intravenous catheter placed in an antecubital vein or an equivalent venous access

Recruiting Locations

Johns Hopkins University
Baltimore, Maryland 21287
Contact:
Yasser Ged, MBBS
410-955-8893
yged1@jhmi.edu

More Details

Status
Recruiting
Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

Study Contact

Yasser Ged, MBBS
410-955-8893
yged1@jhmi.edu

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.