A Phase 2 Diagnostic Imaging Study With 99mTc-MIP-1404 in Men With High-Risk Prostate Cancer Scheduled for Radical Prostatectomy (RP) and Extended Pelvic Lymph Node Dissection (EPLND) Compared to Histopathology



Status:Completed
Conditions:Prostate Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:21 - Any
Updated:4/21/2016
Start Date:August 2012
End Date:December 2013

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A Phase 2 Assessment of the Diagnostic Accuracy of 99mTc-MIP-1404 Imaging in Men With High-Risk Prostate Cancer Scheduled for Radical Prostatectomy (RP) and Extended Pelvic Lymph Node Dissection (EPLND) Compared to Histopathology

This is a single arm, open label study of approximately 100 high-risk prostate cancer
patients scheduled for prostatectomy and extended 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 extended
pelvic lymph node dissection (EPLND) within three weeks of study drug dosing. 99mTc-MIP-1404
image data will be evaluated for visible uptake and compared with histopathology.


Inclusion Criteria:

- Male aged 21 years or older.

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

- Biopsy confirmed presence of adenocarcinoma of the prostate gland.

- At high-risk for metastatic disease by a stage of cT3, cT4, or a total nomogram score
of greater than or equal to 130.

- Scheduled to undergo radical prostatectomy with extended pelvic lymph node
dissection.

- Agree to use an acceptable form of birth control for a period of 7 days after the
99mTc MIP-1404 injection.

Exclusion Criteria:

- Participating would significantly delay the scheduled standard of care therapy.

- Administered a radioisotope within 5 physical half lives prior to study drug
injection.

- Have 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.

- Have a contraindication for MR imaging.
We found this trial at
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Rochester, Minnesota 55905
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171 Ashley Avenue
Charleston, South Carolina 29425
843-792-1414
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2301 Erwin Rd
Durham, North Carolina 27710
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Madison, Wisconsin 53792
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New York City, New York 10021
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