EUCTR2012-001864-30-HU
Active, not recruiting
Not Applicable
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
ConditionsProstate Cancer within prostate gland and metastatic prostate cancer in regional lymph nodesMedDRA version: 15.0Level: LLTClassification code 10007113Term: Cancer of prostateSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)Therapeutic area: Diseases [C] - Cancer [C04]
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Prostate Cancer within prostate gland and metastatic prostate cancer in regional lymph nodes
- Sponsor
- Molecular Insight Pharmaceuticals, Inc
- Enrollment
- 100
- Status
- Active, not recruiting
- Last Updated
- 12 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Subjects must meet all of the following criteria to be enrolled in this study:
- •1\. Male aged 21 years or older.
- •2\. Ability to provide signed informed consent and willingness to comply with protocol requirements.
- •3\. Biopsy confirmed presence of adenocarcinoma of the prostate gland.
- •4\. At high\-risk for metastatic disease by a stage of cT3, cT4, or a total nomogram score of greater than or equal to 130
- •5\. Scheduled to undergo radical prostatectomy with extended pelvic lymph node dissection.
- •6\. Agree to use an acceptable form of birth control for a period of 7 days after the 99mTc\-MIP\-1404 injection
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) yes
Exclusion Criteria
- •Subjects must not meet any of the following criteria to be enrolled in this study:
- •1\. Participating would significantly delay the scheduled standard of care therapy.
- •2\. Administered a radioisotope within 5 physical half lives prior to study drug injection.
- •3\. 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.
- •4\. Have a contraindication for MR imaging.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Active, not recruiting
Phase 1
A clinical study in men with prostate cancer undergoing surgery to assess the accuracy of 99mTc-MIP-1404 imaging as compared to pathology resultsProstate Cancer within prostate gland and metastatic prostate cancer in regional lymph nodesMedDRA version: 14.1Level: LLTClassification code 10007113Term: Cancer of prostateSystem Organ Class: 100000004864Therapeutic area: Diseases [C] - Cancer [C04]EUCTR2012-001864-30-BEMolecular Insight Pharmaceuticals, Inc100
Active, not recruiting
Phase 1
Phase 2 study to assess the effectiviness of the investigational drug 99mTc-MIP-1404 in detecting prostate cancer tissue within the prostate gland and elsewhere in human body.Prostate Cancer within prostate gland and metastatic prostate cancer in regional lymph nodesMedDRA version: 14.1Level: LLTClassification code 10007113Term: Cancer of prostateSystem Organ Class: 100000004864Therapeutic area: Diseases [C] - Cancer [C04]EUCTR2012-001864-30-CZMolecular Insight Pharmaceuticals, Inc100
Active, not recruiting
Not Applicable
A clinical study in men with prostate cancer undergoing surgery to assess the accuracy of 99mTc-MIP-1404 imaging as compared to pathology resultsProstate Cancer within prostate gland and metastatic prostate cancer in regional lymph nodesMedDRA version: 14.1Level: LLTClassification code 10007113Term: Cancer of prostateSystem Organ Class: 100000004864Therapeutic area: Diseases [C] - Cancer [C04]EUCTR2012-001864-30-NLMolecular Insight Pharmaceuticals, Inc100
Recruiting
Not Applicable
Pilot study of 68Ga-Pentixafor positron emission tomography (PET) imaging in multiple myelomaACTRN12617000593336Royal Brisbane and Women's Hospital10
Not yet recruiting
Not Applicable
Retrospective study of the diagnostic accuracy of CT scan in evaluation of resectability of Boderline resectable pancareatic cancer after neoadjuvant S-1 and concurrent radiotherapyBorderline resectable pancreatic cancerJPRN-UMIN000029166ational Cancer Centor Japan53