Pilot Study of 99mTc-MIP-1404 SPECT/CT Imaging in Men With Prostate Cancer Undergoing Prostatectomy and/or Pelvic Lymph Node Dissection



Status:Completed
Conditions:Prostate Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:21 - Any
Updated:4/21/2016
Start Date:January 2012

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A Phase 1 Pilot Study of 99mTc-MIP-1404 Single Photon Emission Computed Tomography (SPECT)/CT Imaging in Men With Prostate Cancer Undergoing Prostatectomy and/or Pelvic Lymph Node Dissection (PLND)

This is a single arm, open label study of up to 24 high risk prostate cancer patients
scheduled for prostatectomy and/or pelvic lymph node dissection. Patients receive a single
IV dose of 99mTc-MIP-1404 (study drug) followed by SPECT/CT scan 3-6 hours after injection.
As standard of care, patients will undergo prostatectomy and/or pelvic lymph node dissection
(PLND) within two weeks of study drug dosing. Patients may receive a second injection of
study drug within 24 hours of surgery to measure activity counts in tissue samples
post-surgery, but prior to pathology processing. 99mTc-MIP-1404 image data will be evaluated
for visible uptake and compared with histopathology.


Inclusion Criteria:

1. Male aged 21 years or older.

2. Ability to provide signed informed consent and willingness to comply with protocol
requirements.

3. Past biopsy indicating the presence of adenocarcinoma of the prostate gland.

4. Participant is deemed to be high-risk with potential for pelvic lymph node
involvement. The criteria for high-risk are:

- Patient has PSA value >10 and clinical stage T2 or higher, and Gleason score 8,
9 or 10.

- Patient has PSA value >20 and clinical stage T2 or higher, and Gleason score

5. Participant is or will be scheduled to undergo standard of care prostatectomy and/or
pelvic lymph node dissection.

6. Have had (within previous 2 months) or will undergo diagnostic CT or MRI imaging
prior to surgery.

7. Have had (within previous 2 months) or will undergo bone scan imaging prior to
surgery.

8. Participants must agree to use an acceptable form of birth control throughout the
study period. Participants must use condoms for a period of seven days after each
injection, if engaged in sexual activity.

Exclusion Criteria:

1. Participants for whom participating would significantly delay the scheduled standard
of care therapy.

2. Participants administered a radioisotope within 5 physical half lives prior to study
enrollment.

3. Participants with any medical condition or other circumstances that, in the opinion
of the Investigator, would significantly decrease obtaining reliable data, achieving
study objectives or completing the study.
We found this trial at
1
site
New York, New York 10021
?
mi
from
New York, NY
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