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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03444844
Other study ID # IU-1711061247
Secondary ID
Status Active, not recruiting
Phase Phase 1/Phase 2
First received
Last updated
Start date May 10, 2018
Est. completion date July 2022

Study information

Verified date April 2022
Source Five Eleven Pharma, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Initial performance of Ga-68-P16-093 in prostate cancer patients including dosimetry and preliminary efficacy evaluation in BCR patients, and correlation of Ga-68-P16-093 uptake with tissue histopathology in intermediate to high risk primary prostate cancer patients.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 60
Est. completion date July 2022
Est. primary completion date October 27, 2020
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria (Cohort 1): - Male = 18 years of age - Prostate cancer patients presenting with rising PSA after radical prostatectomy for treatment if primary disease. - PSA = 0.2 ng/mL - Patients must give informed consent for the research study, and agree to allow investigator access to clinical results following treatment plan implementation such as description of the treatment plan and PSA values following implementation of treatment plan as part of standard care, typically determined 3-4 months after treatment. Inclusion Criteria (Cohort 2): - Male = 18 years of age - Histologically confirmed prostate cancer with following Gleason scoring at biopsy: - Gleason = 4+3 OR - Gleason 3+4 with >30% pattern 4 or =3 cores positive - Scheduled for radical prostatectomy (expected to occur within 60-days of scanning) - Patients must give informed consent for the research study, and agree to allow investigator access to the clinical results such as SOC imaging (mpMRI, e.g.) for surgical planning if done, or biopsy data following prostatectomy including lymph node dissection biopsy data, if available. Exclusion Criteria (Cohorts 1& 2): - Inability to give informed consent. - Patient is unable to tolerate remaining still on the bed of the PET camera, due to physical limitations or claustrophobia. - Significant acute or chronic medical, neurologic, or illness in the subject that, in the judgment of the Clinical Investigators, could compromise subject safety, limit the ability to complete the study, and/or compromise the objectives of the study

Study Design


Intervention

Drug:
Ga-68 P16-093 PET/CT scan
IV injection followed by PET/CT scanning

Locations

Country Name City State
United States Goodman Hall, Indiana Institute for Biomedical Imaging Sciences, Indiana University School of Medicine Indianapolis Indiana

Sponsors (2)

Lead Sponsor Collaborator
Five Eleven Pharma, Inc. Indiana University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sensitivity of Ga-68-P16-093 in BCR We will compare the number and location of metastatic lesions apparently detected by 68Ga-P16-093 with the number and location of lesions detected by standard-of-care imaging. Sensitivity of the 68Ga-P16-093 PET procedure will be estimated based on the number of subjects in whom a site of disease is identified by the imaging procedure. Scans will also be reconstructed summing passes 1-5, passes 2-5, passes 3-5, and passes 1-2 to assess how image quality varies with chosen framing. 2 weeks
Primary The proportion of patients for whom Ga-18-P16-093 PET/CT changes treatment through detection of lesions Change in management will be based on physician questionnaires including confirmation of actual treatment. 4 months
Primary Sensitivity and Specificity of Ga-68-P16-093 in primary PCa We will estimate the sensitivity and specificity of the 68Ga-P16-093 PET imaging by comparing the PET SUV values and whole-mount pathology findings on a sextant basis (6 sextants per subject x 10 subjects). Images will be evaluated from ~ 5 min to 60 minutes of scanning in 5-10 minutes up to 45 min frames. 2-60 days following PET/CT scan
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