Evaluation of a Targeted Magnetic Resonance Imaging Contrast Agent in Prostate Cancer Patients
Recruiting · NCT06262139 · Interventional (participants receive a specific treatment) · Lead sponsor: Songqi Gao
View the official record on ClinicalTrials.gov →Interventions studied
MT218 injection
What this trial is about
This phase 1b open label, dose-escalating investigation study is to evaluate the dose dependent initial efficacy of the use of MT218 injection for biomarker targeted MR molecular imaging (MRMI) of prostate cancer in patients scheduled for radical prostatectomy.
Who can take part
Age range
18 Years to 90 Years
Sex
Male
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 1, Phase 2
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Male subjects aged \>18 years.
- Patients with confirmed Gleason score of 8 - 10 prostate cancer, had at least one prostate mpMRI and one prostate biopsy.
- Ability to lie still for MRI scanning.
- Patients must be able to provide written informed consent.
- Glomerular filtration rate (GFR) \> 60 mL/min within a 30 days of the research MRI.
- Key
Exclusion criteria
- Any diagnosis of active acute, chronic, or sub-chronic kidney or liver disease.
- Documented acute prostatitis, symptomatic or severe benign prostatic hyperplasia (BPH) or urinary tract infections.
- Patients with uncontrolled diabetes or hypertension.
- Patients with active non-prostate malignancy.
- Patients with contraindications for MRI including implantable pace makers, cochlear implants.
- Patients with uni- or bilateral hip prosthesis.
- Subjects with other significant medical conditions that would create unacceptable operative risk, compromise retention on study or compromise study related assessments.
- Major surgery within 4 weeks prior to entry on this study or patients who have not recovered from side effects of such therapy.
- Prostate biopsy within 4 weeks prior to entry on this study in which inflammation might affect MRI result.
- Subjects who received or will receive any other MRI contrast agent within 48 hours prior to MT218 injection or up to 24 hours after MT218 injection.
- Is determined by the investigator that the patient is clinically unsuitable for the study.
- Is incapable of understanding the language in which the information for the patient is given.
- Participation in a concurrent clinical trial or in another trial within the past 30 days.
Where it is running
1 location listed across 1 US state.
- Emory University - Atlanta, Georgia, United States