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 @ 2:45 PM
Ignite Modification Date:
2025-12-24 @ 2:45 PM
NCT ID:
NCT00959959
Eligibility Criteria:
Inclusion Criteria:
* Signed informed consent form
* Confirmed cancer of the prostate
* Progressing disease in spite of androgen ablation therapy
* Able to swallow multiple capsules
Exclusion Criteria:
* Participation in another clinical trial \< 4 weeks prior to enrollment
* Metastatic disease with one or more of the following:
* Liver involvement
* Bone pain associated with confirmed evidence of metastases
* Non-hepatic visceral involvement
* The following medications:
* Prior treatment with MDV3100, abiraterone, Provenge or TAK700
* Prior treatment with ketoconazole
* Prior treatment with chemotherapy
* Prior radiation therapy completed ≤ 4 weeks prior to enrollment
* The following medical conditions:
* Active angina pectoris
* History of Hepatitis B or Hepatitis C
* Known HIV infection
* Ongoing hypertension
Note: There are additional inclusion and exclusion criteria. The clinical site center will determine if you are eligible. If you are not eligible for the trial, site staff will detail the reasons to you.
Healthy Volunteers:
False
Sex:
MALE
Minimum Age:
18 Years
Study:
NCT00959959
Study Brief:
Protocol Section:
NCT00959959