Status:

ACTIVE_NOT_RECRUITING

Biodistribution and Dosimetry of Ga-68 P16-093 in Prostate Cancer

Lead Sponsor:

Five Eleven Pharma, Inc.

Collaborating Sponsors:

Indiana University

Conditions:

Prostate Cancer Recurrent

Prostate Cancer

Eligibility:

MALE

18+ years

Phase:

PHASE1

PHASE2

Brief 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 histopatho...

Eligibility Criteria

Inclusion

  • 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

Exclusion

    Key Trial Info

    Start Date :

    May 10 2018

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ESTIMATED

    End Date :

    July 1 2022

    Estimated Enrollment :

    60 Patients enrolled

    Trial Details

    Trial ID

    NCT03444844

    Start Date

    May 10 2018

    End Date

    July 1 2022

    Last Update

    May 2 2022

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    Goodman Hall, Indiana Institute for Biomedical Imaging Sciences, Indiana University School of Medicine

    Indianapolis, Indiana, United States, 46202