Status and phase
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About
This is a single-blind, randomized, cross-over design. Patients with metastatic prostate adenocarcinoma; newly diagnosed, high-risk patients with prostate adenocarcinoma; and healthy subjects will be administered a single intravenous dose of each of the study drugs 99mTc MIP 1404 and 99mTc MIP 1405 administered approximately 14 to 21 days apart.
Full description
This trial is a single-blind, randomized, cross-over design. Up to six patients with confirmed metastatic prostate adenocarcinoma; six newly diagnosed, high-risk patients with prostate adenocarcinoma; and up to six healthy volunteers will receive 20.0 (± 3) mCi of intravenously administered 99mTc MIP 1404 or 99mTc MIP 1405. Whole-body planar scintigraphic images will be acquired at various times post-injection over 24 hours. A pelvic SPECT/CT image will be acquired on the first day. Blood and urine will be collected for pharmacokinetic measurements and metabolic analysis over 24 hours. Each patient will receive an initial study drug administration and a second study drug administration approximately 14 to 21 days after the first. A final follow-up visit will occur approximately 2-3 weeks after the second study drug.
Enrollment
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Volunteers
Inclusion criteria
Participants must meet all of the following criteria to be enrolled in this study.
Additional Inclusion Criteria for Patients:
i. Histologic diagnosis of prostate cancer by validated medical history. (Pathology report, if available).
ii. Evidence of metastatic disease demonstrated by a documented abnormal bone scan, CT scan, or MRI plus a Clinical Stage 3 and Gleason Score ≥ 8.
iii. Karnofsky performance is ≥ 60.
Additional Inclusion Criteria for Healthy Volunteers:
i. PSA laboratory assessment within normal range (PSA < 4 ng/ml). ii. Normal findings on a digital rectal examination. iii. Hemoglobin and hematocrit within normal range.
Exclusion criteria
Participants must NOT meet any of the following criteria to be enrolled in this study.
Additional Exclusion Criteria for Patients:
Patients will be excluded from the study if any of the following criteria are observed:
i. Androgen deprivation therapy or other forms of hormonal therapy not stable for a period of 14 days prior to screening.
ii. Subject has received a permanent prostate brachytherapy implant within the last 3 months for 103Pd implants; or 12 months for 125I implants.
iii. Subject on or expected to be starting cytotoxic chemotherapy during the study period.
iv. Has had any other malignancies within the past year, other than basal or squamous cell carcinoma of the skin, diagnosis and location must be defined or be defined as clinically controlled or treated to complete response.
Additional Exclusion Criteria for Healthy Volunteers:
Healthy Volunteers will be excluded from the study if any of the following criteria are observed:
i. Have had any malignancies within 5 years other than basal or squamous cell carcinoma of the skin.
ii. History of known prostate adenocarcinoma, prostate surgery/biopsy, prostatitis and/or symptoms suggestive of or associated with possible prostatitis within 6 months of enrollment.
Primary purpose
Allocation
Interventional model
Masking
16 participants in 3 patient groups
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Data sourced from clinicaltrials.gov
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