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Approved for marketingNCT02355054Updated Jan 20, 2017

Detecting Recurrent Prostate Cancer With C-11 Choline Positron Emission Tomography: An Expanded Access Study

An expanded access record providing C-11 Choline PET Imaging in Cancer of the Prostate, sponsored by Washington University School of Medicine. Approved for marketing at 1 site in United States. Open to male participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-01-20.

Sponsored by Washington University School of Medicine · Expanded access

Study type
Expanded access
Ages
18 Years and older
Sex
Male
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Study summary

The purpose of this study is to provide clinical access to PET/CT and PET/MRI with C-11 choline for evaluation of men with biochemically recurrent prostate cancer while awaiting approval of the Washington University Abbreviated New Drug Application for C-11 choline.

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Conditions studied

  • Cancer of the Prostate

Keywords

  • Recurrent
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In context

Prostatic Neoplasms

6,484 studies on the registry are indexed under Prostatic Neoplasms; 1,415 are open to participants now.

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Lead sponsor

Washington University School of Medicine is the lead sponsor of 1,795 studies on the registry; 271 are open to participants now.

Of its 330 completed or terminated interventional studies of FDA-regulated products, 216 (65%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Male

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Patient must have biopsy-proven adenocarcinoma of the prostate initially treated with curative intent (surgery and radiation therapy are most common treatments but other treatments are also eligible).
  2. Biochemical recurrence defined as any of the following:

    • PSA ≥ 0.2 ng/mL in at least two sequential tests for patients treated with surgery.
    • PSA ≥ 2.0 ng/mL above the post therapy nadir for patients treated with radiation therapy, brachytherapy or cryotherapy.
    • PSA ≥ 2.0 ng/ml above the most recent therapy nadir for patients who have received additional treatment in the recurrent setting.
  3. Patient must have undergone standard-of-care restaging that does not clearly identify site(s) of active disease. Standard staging examinations may include one or more of the following: CT or MRI, bone imaging (either Tc-99m bisphosphonate scintigraphy or F-18 sodium fluoride PET), OR In-111 capromab pendetide scintigraphy.
  4. Age > 18 years.
  5. Patient must be able to tolerate PET/MRI or PET/CT imaging
  6. Patient must be able to understand and willing to sign a written informed consent document.
  7. Patient must be able to understand and willing to sign an Advance Beneficiary Notice (ABN) (Medicare patient) or a Notice of Non-coverage (NNC) from (non-Medicare patient) that addresses the potential cost to the patient of C-11 choline PET/CT or PET/MRI.

Exclusion criteria

Exclusion Criteria:

  1. For patients planned to have PET/MRI:

    • Patient must not have claustrophobia or any other contraindication to MRI as evaluated by a standardized MRI safety questionnaire.
    • If applicable, patient must not have renal insufficiency (estimated glomerular filtration rate \< 30 mL/min/1.73 m2 based on measurement within the past 60 days) or be undergoing dialysis as these conditions preclude safe administration of MRI contrast agents. NOTE: At the discretion of principal investigator, a subject may be allowed to enroll/continue on study and undergo imaging without the administration of contrast in the event of renal insufficiency.
    • If applicable, patient must not have a known prior reaction to gadolinium based MRI contrast agents.
  2. For patients planned to have PET/CT:

    • Patient must not have claustrophobia that would preclude PET/CT imaging or other contraindications to CT imaging.
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Access details

Study type
Expanded access

Available treatment

  • DrugC-11 Choline PET Imaging

    Patients will receive IV injection of C-11 Choline followed by imaging from the base of the brain to the upper thigh on a PET/CT or a PET/MRI scanner

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Where to request access

1 site
  • Washington University School of Medicine, Barnes-Jewish Hospital
    St Louis, Missouri 63110, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 20, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02355054
Responsible party
Farrokh Dehdashti (Professor of Radiology, Washington University School of Medicine) — Principal investigator
First posted
Feb 4, 2015
Last update
Jan 20, 2017
View the source record on ClinicalTrials.gov ↗

Requesting access

Expanded access is arranged between your doctor and the company. Ask your care team to contact the provider listed on this record.

No contact was published for this record. The registry link below has the sponsor’s details.

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Discussion

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