Overview
Abiraterone and Prednisone or Darolutamide for the Treatment of Advanced Prostate Cancer
Status:
Recruiting
Recruiting
Trial end date:
2027-05-01
2027-05-01
Target enrollment:
0
0
Participant gender:
Male
Male
Summary
This phase II trial compares the effects, good and/or bad of abiraterone and prednisone or darolutamide alone in treating patients with prostate cancer that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Androgens (male hormones) can cause the growth of prostate tumor cells. Abiraterone acetate lowers the amount of androgens made by the body. This may help stop the growth of prostate tumor cells that need androgen to grow. Darolutamide blocks the use of androgens by the tumor cells. Prednisone is used to lessen inflammation and lower the body's immune response. Researchers want to compare the side effects of standard of care (SOC) abiraterone and prednisone or darolutamide alone in treating patients with advanced prostate cancer.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Mamta ParikhCollaborator:
National Cancer Institute (NCI)Treatments:
Androgen Antagonists
Cortisone
Prednisone
Criteria
Inclusion Criteria:- Ability to understand and willingness to sign an informed consent form
- Histologically confirmed prostate adenocarcinoma
- Advanced prostate cancer appropriate for treatment with abiraterone acetate plus
prednisone or darolutamide as assessed by the treating physician
- Participants are encouraged to be currently treated with androgen deprivation therapy
(ADT) or having undergone bilateral orchiectomy
- Performance status 0 - 2 (Karnofsky ≥ 50%)
- Age ≥ 18 years at time of consent
- Life expectancy ≥ 6 months per investigator discretion
- Ability and stated willingness to adhere to the study visit schedule and other
protocol procedures/requirements for the duration of the study
Exclusion Criteria:
- Have been on either abiraterone or darolutamide for > 28 days prior to initiating
enrollment
- Any condition that in the opinion of the investigator would prohibit the understanding
or rendering of informed consent or interfere with the participant's safety or
compliance while on trial