A Study for Subjects With Prostate Cancer Who Previously Participated in an Enzalutamide Clinical Study

Recruiting now · Phase 2

Conditions studied: Prostate Cancer

In brief

The purpose of this study is to collect long term safety data in subjects who are continuing to derive clinical benefit from treatment with Enzalutamide from the subjects participation in an enzalutamide clinical study sponsored by Astellas or Medivation (i.e., parent study) which has completed, at a minimum, the primary analysis or the study specified evaluation period.

Key facts

Study ID

NCT02960022

Run by

Astellas Pharma Global Development, Inc.

People needed

900

Starts

2016-12-22

Expected to finish

2029-07-31

Last updated by the study team

2026-07-31

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Subject must currently be receiving enzalutamide or assigned to receive enzalutamide (if on treatment suspension) for prostate cancer in a study sponsored by Astellas or Medivation and, based on the investigator's assessment, benefit from continued treatment. Subjects participating in investigator-initiated trials are not eligible.
• Subject is able to continue on the treatment regimen that they were receiving or were assigned to receive in the prior study. If in the investigator's assessment, a change is needed to the subject's regimen (e.g., dose change in Androgen deprivation therapy (ADT) or dropping of a combination therapy) approval from a medical monitor is required prior to enrollment.
• Subject is able to swallow enzalutamide capsules and comply with study requirements.
• Subject and female partner who is of childbearing potential must continue to use 2 forms of birth control, of which 1 must be highly effective and 1 must be a barrier method throughout the study and for 3 months after final enzalutamide administration.
• Subject agrees to avoid sperm donation during the study and for at least 3 months after final enzalutamide administration.
• Subject agrees not to participate in another interventional study while on treatment.
• Canada Specific:
• Institutional Review Board (IRB)/Independent Ethics Committee (IEC) approved written Informed Consent and privacy language as per national regulations (e.g., Health Insurance Portability and Accountability Act authorization for the United States sites) must be obtained from the subject prior to any study-related procedures.
• Subject must currently be receiving enzalutamide for breast cancer in a study sponsored by Astellas or Medivation/Pfizer and based on the investigator's assessment, benefit from continued treatment. Subjects participating in investigator-initiated trials are not eligible.
• Subject is able to continue on the treatment regimen that they were receiving in the prior study. If in the investigator's assessment, a change is needed to the subject's regimen (e.g., dropping of a combination therapy) approval from a medical monitor is required prior to enrollment.
• Subject is able to swallow enzalutamide capsules and comply with study requirements.
• Subject is either:
• Of nonchildbearing potential:
• postmenopausal (defined as no spontaneous menses for at least 12 months prior to Day 1 with follicle stimulating hormone (FSH) > 40 IU/L at Day 1 for women < 55 years of age),
• documented surgically sterile or status post hysterectomy (at least 1 month prior to Day 1),
• Or, if of childbearing potential,
• must have a negative urine pregnancy test at Day 1 before the first dose of study drug is administered,
• must use 2 acceptable methods of birth control starting at Day 1 and through 6 months after the final study drug administration,
• must not donate ova starting at first administration of study intervention and throughout 6 months after final study intervention administration.
• The 2 acceptable methods of birth control are as follows or per local guidelines where these require additional description of contraceptive methods:
• A barrier method (e.g., condom by a male partner) is required; AND
• One of the following is required:
• Placement of an intrauterine device (IUD) or intrauterine system (IUS);
• Additional barrier method including occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/suppository;
• Vasectomy or other surgical castration at least 6 months before Day 1.

You may not qualify if…

• Subject met any of the discontinuation criteria or whose cancer progressed on the current enzalutamide clinical study in which subject is enrolling from.
• Subject requires treatment with or plans to use either of the following:
• New systemic therapy for subjects cancer (palliative radiation therapy is allowed). The treatment with agents administered during previous studies which was stopped and then restarted during this study does not represent new treatment.
• Investigational therapy other than enzalutamide.
• Subject is currently participating in an investigator-initiated interventional trial and receiving enzalutamide.
• Subject has any concurrent disease, infection, or comorbid condition that interferes with the ability of the subject to participate in the study, which places the subject at undue risk or complicates the interpretation of data.
• Canada Specific:
• Subject will be excluded from participation if any of the following apply:
• Subject met any of the discontinuation criteria or whose cancer progressed on the current enzalutamide clinical study in which they are enrolling from.
• Subject requires treatment with or plans to use any of the following:
• New systemic therapy for their cancer (palliative radiation therapy is allowed). The treatment with agents administered during previous studies which was stopped and then restarted during this study does not represent new treatment.
• Investigational therapy other than enzalutamide.
• Subject is currently participating in an investigator-initiated interventional trial and receiving enzalutamide.
• Subject has any concurrent disease, infection, or comorbid condition that interferes with the ability of the subject to participate in the study, which places the subject at undue risk or complicates the interpretation of data in the opinion of the investigator.

Where it is running

• Site US10067 — Orange, California, United States (enrolling)
• Site IL97206 — Haifa, Israel (enrolling)
• Site BR55004 — Ijuí, Brazil (enrolling)
• Site US10040 — Los Angeles, California, United States
• Site US10008 — San Bernardino, California, United States
• Site US10042 — San Diego, California, United States
• Site US10017 — Denver, Colorado, United States
• Site US10001 — Aurora, Colorado, United States
• Site US10032 — St Louis, Missouri, United States
• Site US10050 — Washington D.C., District of Columbia, United States
• Site US10049 — Daytona Beach, Florida, United States
• Site US10048 — Jacksonville, Florida, United States
• Site US10002 — Chicago, Illinois, United States
• Springfield Clinic, LLP — Springfield, Illinois, United States
• University of Kansas Medical Center — Kansas City, Kansas, United States
• Site US10007 — Jeffersonville, Indiana, United States
• Site US10066 — Lenexa, Kansas, United States
• Site US10029 — Towson, Maryland, United States
• Site US10028 — Stanford, California, United States
• Nebraska Medical Hospital — Omaha, Nebraska, United States
• Site US10023 — Omaha, Nebraska, United States
• Site US10004 — Hackensack, New Jersey, United States
• Site US10024 — Garden City, New York, United States
• Site US10055 — New York, New York, United States
• Site US10009 — Los Angeles, California, United States

Full record on ClinicalTrials.gov

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