REDECT 2: REnal Masses: Pivotal Trial to DEteCT Clear Cell Renal Cell Carcinoma With PET/CT
Primary Purpose
Renal Cell Carcinoma, Kidney Cancer
Status
Withdrawn
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Iodine (124I) Girentuximab
Sponsored by
About this trial
This is an interventional diagnostic trial for Renal Cell Carcinoma
Eligibility Criteria
Inclusion Criteria:
- ≥18 years of age.
- Presence of indeterminate cT1 renal mass by screening CT with and without contrast or MRI with and without contrast (MRI only if CT is contra-indicated).
- Negative serum pregnancy test; to be performed on female patients of childbearing potential within 24 hours prior to receiving investigational product.
- Recovered from toxicity of any prior therapy to grade 1 or better.
- Able to take oral medication (KI).
- Written informed consent available.
Exclusion Criteria:
- Renal mass known to be a metastasis of another primary tumor.
- Known histology of renal mass (e.g. by biopsy).
- Active non-renal malignancy requiring therapy during the time frame of individual patient study participation.
- Chemotherapy, radiotherapy, or immunotherapy within 4 weeks prior to Iodine (124I) Girentuximab infusion on Day 0 or continuing adverse effects (>grade 1) from such therapy.
- Exposure to murine proteins or chimeric antibodies within the last 5 years.
- Intercurrent medical condition that may limit patient's study participation or compliance.
- History of autoimmune hepatitis.
- Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study.
- Participation in any other clinical trial involving another investigational product within 4 weeks prior to enrollment.
- Women who are pregnant or breastfeeding.
- Contraindication to KI intake (see package insert/Appendix VI).
- Hyperthyroidism, or Grave's Disease.
- Contraindication for PET/CT.
Sites / Locations
- David Geffen School of Medicine, UCLA
- H. Lee Moffitt Cancer Center & Research Center
- Lahey Clinic
- Memorial Sloan-Kettering Cancer Center
- Duke University Medical Center
- Ohio State University
- Fox Chase Cancer Center
- MD Anderson
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Iodine (124I) Girentuximab
Arm Description
Single infusion of radio labeled antibody: 30 mL will be infused using an infusion pump at a rate of 2mL/min over 15 minutes on study day 0.
Outcomes
Primary Outcome Measures
Sensitivity and specificity of Iodine (124I) Girentuximab PET/CT scans will be compared to the threshold value of 0.70 using a two-sided exact binomial test at level 0.05.
Secondary Outcome Measures
Full Information
NCT ID
NCT01762592
First Posted
December 19, 2012
Last Updated
December 20, 2017
Sponsor
Heidelberg Pharma AG
1. Study Identification
Unique Protocol Identification Number
NCT01762592
Brief Title
REDECT 2: REnal Masses: Pivotal Trial to DEteCT Clear Cell Renal Cell Carcinoma With PET/CT
Official Title
A Study of Iodine (124I) Girentuximab PET/CT Scan for the Detection of Clear Cell Renal Cell Carcinoma in Patients With Indeterminate cT1 Renal Masses
Study Type
Interventional
2. Study Status
Record Verification Date
December 2017
Overall Recruitment Status
Withdrawn
Why Stopped
new sponsor
Study Start Date
December 2017 (Anticipated)
Primary Completion Date
December 1, 2018 (Anticipated)
Study Completion Date
December 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Heidelberg Pharma AG
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Study WX-20-002 will confirm diagnostic efficacy and safety of a PET/CT scan using Iodine (124I) Girentuximab performed during the diagnostic work-up in patients with indeterminate cT1-renal masses.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Cell Carcinoma, Kidney Cancer
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Iodine (124I) Girentuximab
Arm Type
Experimental
Arm Description
Single infusion of radio labeled antibody: 30 mL will be infused using an infusion pump at a rate of 2mL/min over 15 minutes on study day 0.
Intervention Type
Drug
Intervention Name(s)
Iodine (124I) Girentuximab
Other Intervention Name(s)
124I-cG250
Intervention Description
i.v.
Primary Outcome Measure Information:
Title
Sensitivity and specificity of Iodine (124I) Girentuximab PET/CT scans will be compared to the threshold value of 0.70 using a two-sided exact binomial test at level 0.05.
Time Frame
PET/CT imaging of the kidneys will be performed 5 (±1) days (Day 4, 5, or 6) after the Iodine (124I) Girentuximab infusion.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
≥18 years of age.
Presence of indeterminate cT1 renal mass by screening CT with and without contrast or MRI with and without contrast (MRI only if CT is contra-indicated).
Negative serum pregnancy test; to be performed on female patients of childbearing potential within 24 hours prior to receiving investigational product.
Recovered from toxicity of any prior therapy to grade 1 or better.
Able to take oral medication (KI).
Written informed consent available.
Exclusion Criteria:
Renal mass known to be a metastasis of another primary tumor.
Known histology of renal mass (e.g. by biopsy).
Active non-renal malignancy requiring therapy during the time frame of individual patient study participation.
Chemotherapy, radiotherapy, or immunotherapy within 4 weeks prior to Iodine (124I) Girentuximab infusion on Day 0 or continuing adverse effects (>grade 1) from such therapy.
Exposure to murine proteins or chimeric antibodies within the last 5 years.
Intercurrent medical condition that may limit patient's study participation or compliance.
History of autoimmune hepatitis.
Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study.
Participation in any other clinical trial involving another investigational product within 4 weeks prior to enrollment.
Women who are pregnant or breastfeeding.
Contraindication to KI intake (see package insert/Appendix VI).
Hyperthyroidism, or Grave's Disease.
Contraindication for PET/CT.
Facility Information:
Facility Name
David Geffen School of Medicine, UCLA
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095-1721
Country
United States
Facility Name
H. Lee Moffitt Cancer Center & Research Center
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States
Facility Name
Lahey Clinic
City
Burlington
State/Province
Massachusetts
ZIP/Postal Code
01805
Country
United States
Facility Name
Memorial Sloan-Kettering Cancer Center
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States
Facility Name
Duke University Medical Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27711
Country
United States
Facility Name
Ohio State University
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
Facility Name
Fox Chase Cancer Center
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104-4283
Country
United States
Facility Name
MD Anderson
City
Houston
State/Province
Texas
ZIP/Postal Code
77030-4009
Country
United States
12. IPD Sharing Statement
Learn more about this trial
REDECT 2: REnal Masses: Pivotal Trial to DEteCT Clear Cell Renal Cell Carcinoma With PET/CT
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