Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Five Eleven Pharma, Inc.
Age
18–any
Sex
MALE
Healthy volunteers
Not accepted
You may be eligible if
DYNAMIC GROUP:
1. Participants will be male ≥ 18 years of age
2. History of histologically confirmed cancer that meets criteria for either a) or b)
1. Prostate cancer with known or suspected recurrent or metastatic disease based on clinical imaging (e.g. CT, bone scan, MRI, ultrasound, FDG PET/CT, FACBC PET/CT) within 12 months of screening. If subject is post curative-intent local treatment (e.g. radical prostatectomy, local radiotherapy, brachytherapy) they must have had no intervening change in cancer treatment.
OR
2. Renal Cell cancer with known or suspected metastatic disease based on clinical imaging (e.g. CT, bone scan, MRI, ultrasound, FDG PET/CT)
3. Participants must be informed of the investigational nature of this study and be willing to provide written informed consent and participate in this study in accordance with institutional and federal guidelines prior to study-specific procedures.
1. Participants will be male ≥ 18 years of age
2. History of prostate cancer that is post curative-intent local treatment (e.g. radical prostatectomy, local radiotherapy, brachytherapy) with clinical PSA levels that meet one of the following criteria
1. Post-Prostatectomy (with or without adjuvant RT): PSA level that is \< 0.2 ng/mL measured over at least 2 consecutive tests OR
2. Post-Radiotherapy: PSA level that has not risen from nadir measured over at least 2 consecutive tests
3. If clinical imaging (e.g. bone scan, CT, MRI, ultrasound, PET/CT) has been done within 3 months of screening as part of standard clinical surveillance it must be negative or equivocal for sites of recurrent or metastatic disease (clinical imaging is not required for enrollment)
4. Participants must be informed of the investigational nature of this study and be willing to provide written informed consent and participate in this study in accordance with institutional and federal guidelines prior to study-specific procedures.
You may not be if
1. Estimated creatinine clearance (eGFR) \< 30 mL/min (calculated from serum creatinine result within 30 days of screening)
2. Chemotherapy or radiation therapy within 2 weeks of screening
3. Inability to tolerate imaging procedures in the opinion of an investigator or treating physician
4. Any current medical condition, illness, or disorder as assessed by medical record review and/or self-reported that is considered by a physician investigator to be a condition that could compromise participant safety or successful completion of the study
BIODISTRIBUTION GROUP:
1. Estimated creatinine clearance (eGFR) \< 30 mL/min (calculated from serum creatinine result within 30 days of screening)
2. Androgen deprivation therapy (ADT) within 3 months prior to screening
3. Chemotherapy or radiation therapy within 2 weeks of screening
4. Inability to tolerate imaging procedures in the opinion of an investigator or treating physician
5. Any current medical condition, illness, or disorder as assessed by medical record review and/or self-reported that is considered by a physician investigator to be a condition that could compromise participant safety or successful completion of the study
Clareo Health | Preliminary Evaluation of Uptake of [68Ga]P16-093 in Metastatic Prostate and Renal Cancer
