Clinical trial · Interventional
Safety Study With the Antibody, cG250, and Isotope, 124-Iodine, to Diagnose Patients With Renal Masses.
Pilot Study of Iodine-124 Labeled Chimeric G250 (124I-cG250) in Presurgical Patients With Renal Masses
NCT00199888CI-TRIAL-00061327completedPhase 1Results postedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this study is to see if an antibody (cG250) attached to a radioactive substance (Iodine-124) safely detects clear cell renal cancer in patients with kidney tumors scheduled for surgery.
Conditions
Conditions (7)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer of Kidney | Malignant Kidney Neoplasm | ALIAS | 0.90 |
| Clear Cell Renal Cell Carcinoma | Clear Cell Renal Cell Carcinoma | ONTOLOGY_EXACT | 0.98 |
| Kidney Cancer | Malignant Kidney Neoplasm | CURATED_EXACT | 0.92 |
| Neoplasms, Kidney | Kidney Neoplasm | ONTOLOGY_EXACT | 0.90 |
| Renal Cancer | — | UNRESOLVED | — |
| Renal Cell Carcinoma (RCC) | Renal Cell Carcinoma | CURATED_BROADER | 0.80 |
| Renal Neoplasms | Kidney Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 124-Iodine-cG250 (124I-cG250) | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- 124I-cG250
- description
- Patients who were scheduled for surgical resection of renal masses received a single intravenous (IV) dose of 10 mg of 5 milliCurie (mCi) /10 mg 124I-cG250. Patients underwent Positron-Emission Tomography/Computed Tomography (PET/CT) imaging of the whole body on at least 2 occasions: once following injection and once immediately prior to surgical resection. Patients were scheduled for surgical resection of their renal masses on day 8.
- interventionNames
- Drug: 124-Iodine-cG250 (124I-cG250)
Primary outcomes (1)
- measure
- Positive Predictive Value (PPV) of 124I-cG250 Based on Positron-Emission Tomography/Computed Tomography (PET/CT) Imaging in the Detection of Clear Cell Renal Cell Carcinoma (RCC) Compared to Pathology of Tumor Mass at Surgical Resection.
- timeFrame
- 8 days
- description
- Patients were listed as PET-positive based on a tumor to nontumor radioactive uptake ratio of \> 3 and PET-negative if less than or equal to 3. The resected renal mass (tumor) was subjected to pathological evaluation, and a diagnosis of clear cell RCC or non-clear cell RCC was made. PPV is the proportion of patients with a positive PET scan who actually have the disease based on pathology. Patients who have a positive PET scan on imaging and clear cell RCC on pathology will be considered true-positives. Patients who have negative PET scans on imaging and non-clear cell RCC on pathology will be considered true-negatives. Patients with positive PET scans on imaging and non-clear cell RCC on pathology will be considered false positives and those with clear cell RCC on pathology but negative PET scans on imaging will be considered false negatives.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Presence of a renal mass. 2. Scheduled for surgical resection of renal mass. 3. Expected survival of at least 3 months. 4. Karnofsky performance scale ≥70. 5. The following laboratory results should be within the following limits within the last 4 weeks prior to study day 1: * Absolute neutrophil count (ANC) ≥ 1.5 x 10E9/L * Platelet count ≥ 100 x 10E9/L * Serum bilirubin ≤ 2.0 mg/dL * Aspartate aminotransferase (AST) ≤ 2.5 x upper limit of normal (ULN) * Alanine aminotransferase (ALT) ≤ 2.5 x ULN * Serum creatinine ≤ 2.0 mg/dL 6. Pregnancy Test to be performed on female patients of childbearing potential within 24-48 hours before administration of radioactive material. 7. Recovered from toxicity of any prior therapy. 8. Able and willing to give valid written informed consent. Exclusion Criteria: 1. Intercurrent medical condition that may limit the amount of antibody to be administered. 2. Intercurrent medical condition that renders the patient ineligible for surgery. 3. New York Heart Association Class III/IV cardiac disease. 4. History of autoimmune hepatitis. 5. Chemotherapy, radiotherapy, or immunotherapy within 4 weeks prior to the first cG250 dose. 6. Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study. 7. Lack of availability for immunological and clinical follow-up assessments. 8. Participation in any other clinical trial involving another investigational agent within 4 weeks prior to enrollment. 9. Women who are pregnant or breastfeeding. 10. Allergy to iodine.
References
Publications (1)
- DERIVEDDivgi CR, Pandit-Taskar N, Jungbluth AA, Reuter VE, Gonen M, Ruan S, Pierre C, Nagel A, Pryma DA, Humm J, Larson SM, Old LJ, Russo P. Preoperative characterisation of clear-cell renal carcinoma using iodine-124-labelled antibody chimeric G250 (124I-cG250) and PET in patients with renal masses: a phase I trial. Lancet Oncol. 2007 Apr;8(4):304-10. doi: 10.1016/S1470-2045(07)70044-X. PMID 17395103