Status:
TERMINATED
Decreasing Dosing Regimens of Abiraterone 500 mg in Men With Prostate Cancer to Find Lowest Recommended Dose.
Lead Sponsor:
University of Chicago
Conditions:
Prostate Cancer
Prostate Adenocarcinoma
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
Doctors leading this study plan to collect new information about the lowest effective dose of abiraterone acetate in study participants with prostate cancer who are taking abiraterone in combination w...
Detailed Description
Doctors leading this study plan to collect new information about the lowest effective dose of abiraterone acetate in study participants with prostate cancer who are taking abiraterone in combination w...
Eligibility Criteria
Inclusion
- Histologically or cytologically confirmed prostate cancer with plans to initiate abiraterone acetate
- Have never received prior abiraterone or other androgen receptor modulators, including enzalutamide, apalutamide, or darolutamide.
- Must have a baseline DHEA-S level of \>20 mg/dL (in order to adequately assess DHEA-S response)
- A minimum washout of 28 days for any other anticancer therapy other than medical or surgical castration, prior to first dose of study drug is required.
- Any other radiotherapy or radionuclide require 28-day washout prior to first dose of study drug.
- Denosumab or zoledronic acid are allowed.
- Eastern Cooperative Oncology Group performance status ≤ 2 (Appendix A).
- Participants must have normal hepatic function as defined by clinical lab values set by the study doctor/research team.
- Ability to understand and the willingness to sign a written informed consent document.
Exclusion
- Therapy with other hormonal therapy, including any dose of megestrol acetate (Megace), finasteride (Proscar), dutasteride (Avodart), or any herbal product known to decrease Prostate-Specific Antigen levels or any systemic corticosteroid (other than prednisone ≤10mg/day) within 4 weeks prior to first dose of study drug.
- Inability to swallow capsules or known gastrointestinal malabsorption.
- Blood pressure that is not controlled despite \> 2 oral agents (SBP \>160 and DBP \>90 documented during the screening period with no subsequent blood pressure readings \<160/100).
- Serum K+ \< 3.5 mmoL/L. Patients with a K+ \< 3.5 mmoL/L are required to have a documented subsequent K+ \>3.5 prior to enrollment to be eligible.
- Serious intercurrent infections or non-malignant medical illnesses that are uncontrolled.
- Active psychiatric illness/social situations that would limit compliance with protocol requirements.
- Serious heart issues/congestive heart failure as assessed by New York Heart Association's definition of class II, class III, or IV congestive heart failure.
- Taking other medications or drugs with strong inhibitors or inducers of CYP3A4 (See Section 8.12 below for list of strong inhibitor or inducers) due to concerning possible drug-drug interactions with abiraterone.
Key Trial Info
Start Date :
January 24 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 16 2024
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT05276492
Start Date
January 24 2023
End Date
November 16 2024
Last Update
October 3 2025
Active Locations (1)
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1
University of Chicago Medicine Comprehensive Cancer Center
Chicago, Illinois, United States, 60637