Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 6:52 PM
Ignite Modification Date:
2025-12-24 @ 6:52 PM
NCT ID:
NCT04509557
Eligibility Criteria:
Inclusion Criteria:
1. Among prostate cancer patients with blood testosterone ≤50ng/dL, mCRPC patients showing radiological progression after standard taxene-based anticancer treatment and 2nd generation hormone agent (abiraterone, enzalutamed, or both)) treatment or patients who are not eligible for such standard medical treatment at the discretion of an investigator or patients who refuse such standard treatment
2. Patients who are positive on the \[18F\]PSMA PET/CT imaging
3. Subjects who were fully informed by an investigator of the study objectives, details, and characteristics of the study drug prior to study enrollment, and had an informed consent form signed by the subject or caretaker or legally acceptable representative
4. Male patients aged 20 years or older
5. Subjects who are sexually active and have a female partner of childbearing potential should meet the followings
* Subjects should consent to practice contraception by continuously using a male condom from screening, throughout the study, and for at least 6 months after the last dose of the study drug
* Subjects should never donate sperms from screening, throughout the study, and for at least 6 months after the last dose of the study drug
* Subjects with a partner who is a woman of childbearing potential (including a pregnant or breastfeeding mother) should consent to maintain sexual abstinence or practice double contraception throughout the study \* Double contraception: Corresponding to 2 or more of the followings - use of a condom, use of a non-hormonal intrauterine device, use of a diaphragm, use of a cervical cap, a sexual partner who has been vasectomized at least 3 months (as of the first screening visit) or a sexual partner medically diagnosed to be sterile
6. ECOG \_ Performance score ≤2
7. Life expectancy ≥6 months
Exclusion Criteria:
1. Subjects determined by an investigator to have a serious medical condition making study conduct difficult
2. Subjects corresponding to the following conditions 1) Glomerular filtration rate ≤40 ml/min, 2) hemoglobin level ≤10.0 g/dL, 3) white cell count ≤4.0 × 109/L, 4) platelet count ≤100 × 109/L, 5) total bilirubin level ≥1.5 x upper normal limit, 6) serum albumin level ≤3.0 g/dL, 7) active ischemic heart disease or heart failure (New York Heart Association Classification III-IV), 8) uncontrolled diabetes/hypertension, 9) hyperkalemia \>6.0 mmol/L
3. Vulnerable subjects (the investigator involved in the study or his/her family, research staff or students of the investigator involved in the study)
4. Patients with a persistent malignancy other than the prostate cancer
5. Patients who participated in a therapeutic clinical trial within the past 30 days and administered an investigational product other than standard treatment
6. Patients are excluded if treatment other than the treatment provided in this study is determined more appropriate as determined by the investigator based on the patient and disease characteristics
Healthy Volunteers:
False
Sex:
MALE
Minimum Age:
20 Years
Study:
NCT04509557
Study Brief:
Protocol Section:
NCT04509557