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Generated: December 15, 2018

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CLINICAL TRIALS PROFILE FOR FLUDEOXYGLUCOSE F-18

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Clinical Trials for Fludeoxyglucose F-18

Trial ID Title Status Sponsor Phase Summary
NCT00001568 Phase II Study of the Role of Anti-CEA Antibody Immunoscintigraphy & Positron Emission Tomography in the Localization of Recurrent Colorectal Carcinoma in Patients With Rising Serum CEA Levels in the Absence of Imageable Disease by Conventional Modal Completed National Cancer Institute (NCI) Phase 2 Positron Emission Tomography (PET scanning) is performed using a total dose of less than 50 mRad per patient visit. Fludeoxyglucose F 18 (FDG) is injected intravenously over 2 min. Initial dynamic images will be obtained over the heart. Emission imaging will work from the midcervical region down to the perineal region. For CEA scanning, radiolabeled antibody, arcitumomab (IMMU-4), is injected intravenously over 5 min. A single photon emission computed tomography (SPECT) transmission scan is performed over the same regions as the emission scans. Total dose from transmission scans should be no more than 20 mRad per patient visit. Patients then undergo exploratory laparotomy performed by two surgeons, one blinded to the results of the CEA-Scan and PET scan. At the completion of all exploration, all identified disease is biopsied for pathologic analysis and any resectable disease is removed. Patients are followed every 3 months for 1 year, every 6 months for the second year, and then after 3 years.
NCT00004152 PET and CT Scans to Evaluate Patients With Stage III or Stage IV Melanoma Completed National Cancer Institute (NCI) Phase 2 RATIONALE: Diagnostic procedures may improve the ability to detect metastatic melanoma and to determine the extent of disease. PURPOSE: Phase II trial to evaluate the effectiveness of PET and CT scans to detect metastatic disease in patients who have stage III or stage IV melanoma.
NCT00004152 PET and CT Scans to Evaluate Patients With Stage III or Stage IV Melanoma Completed Memorial Sloan Kettering Cancer Center Phase 2 RATIONALE: Diagnostic procedures may improve the ability to detect metastatic melanoma and to determine the extent of disease. PURPOSE: Phase II trial to evaluate the effectiveness of PET and CT scans to detect metastatic disease in patients who have stage III or stage IV melanoma.
NCT00004867 Positron Emission Tomography in Determining Stage of Esophageal Cancer Completed National Cancer Institute (NCI) N/A RATIONALE: Imaging procedures such as positron emission tomography may improve the ability to determine the stage of esophageal cancer. PURPOSE: This clinical trial is studying how well fludeoxyglucose F 18 positron emission tomography determines tumor stage in patients with esophageal cancer.
NCT00004867 Positron Emission Tomography in Determining Stage of Esophageal Cancer Completed Alliance for Clinical Trials in Oncology N/A RATIONALE: Imaging procedures such as positron emission tomography may improve the ability to determine the stage of esophageal cancer. PURPOSE: This clinical trial is studying how well fludeoxyglucose F 18 positron emission tomography determines tumor stage in patients with esophageal cancer.
NCT00004891 PET and CT Scans in Patients With Locally Advanced Primary Rectal Cancer That Can Be Removed During Surgery Completed National Cancer Institute (NCI) N/A RATIONALE: Diagnostic procedures, such as PET and CT scans, may improve the ability to detect the extent of locally advanced primary rectal cancer and may also help to measure a patient's response to treatment. PURPOSE: This clinical trial is studying how well PET and CT scans detect residual or metastatic disease in patients with locally advanced primary rectal cancer that can be removed during surgery.
NCT00004891 PET and CT Scans in Patients With Locally Advanced Primary Rectal Cancer That Can Be Removed During Surgery Completed Memorial Sloan Kettering Cancer Center N/A RATIONALE: Diagnostic procedures, such as PET and CT scans, may improve the ability to detect the extent of locally advanced primary rectal cancer and may also help to measure a patient's response to treatment. PURPOSE: This clinical trial is studying how well PET and CT scans detect residual or metastatic disease in patients with locally advanced primary rectal cancer that can be removed during surgery.
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for Fludeoxyglucose F-18

Condition Name

Condition Name for Fludeoxyglucose F-18
Intervention Trials
Lymphoma 14
Lung Cancer 9
Breast Cancer 7
Cervical Adenocarcinoma 4
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Condition MeSH

Condition MeSH for Fludeoxyglucose F-18
Intervention Trials
Lymphoma 24
Lung Neoplasms 19
Carcinoma 16
Sarcoma 16
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Clinical Trial Locations for Fludeoxyglucose F-18

Trials by Country

Trials by Country for Fludeoxyglucose F-18
Location Trials
United States 975
Canada 62
Australia 12
Puerto Rico 6
New Zealand 6
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Trials by US State

Trials by US State for Fludeoxyglucose F-18
Location Trials
Maryland 42
California 41
Ohio 41
Pennsylvania 35
New York 34
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Clinical Trial Progress for Fludeoxyglucose F-18

Clinical Trial Phase

Clinical Trial Phase for Fludeoxyglucose F-18
Clinical Trial Phase Trials
Phase 4 2
Phase 3 10
Phase 2/Phase 3 1
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Clinical Trial Status

Clinical Trial Status for Fludeoxyglucose F-18
Clinical Trial Phase Trials
Completed 43
Recruiting 28
Active, not recruiting 26
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Clinical Trial Sponsors for Fludeoxyglucose F-18

Sponsor Name

Sponsor Name for Fludeoxyglucose F-18
Sponsor Trials
National Cancer Institute (NCI) 97
University of Washington 8
Sidney Kimmel Comprehensive Cancer Center 5
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Sponsor Type

Sponsor Type for Fludeoxyglucose F-18
Sponsor Trials
Other 104
NIH 99
Industry 15
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Serving hundreds of leading biopharmaceutical companies globally:

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Colorcon
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