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Estrogen to Improve Quality of Life for Men With Newly Diagnosed or Recurrent Metastatic Hormone Sensitive Prostate Cancer, EQUIP Trial

StatusNot Yet Recruiting
PhasePhase 2
Started2026-11-01
View on ClinicalTrials.gov ↗

Amendment history

2026-08-27
notable
Study Identification, Study Status, Sponsor/Collaborators v2
Sponsor changed: University of Washington → Fred Hutchinson Cancer Center+5 characters
WasUniversity of Washington
NowFred Hutchinson Cancer Center
2026-08-10
minor
Study Status v1
Start date2026-08-01→2026-11-01
2026-03-09
minor
Original filing
This phase II trial compares giving estrogen with an androgen receptor signaling inhibitor to standard of care luteinizing hormone-releasing hormone (LHRH) analogues with an androgen receptor signaling inhibitor for improving quality of life for patients with hormone sensitive prostate cancer that is newly diagnosed or that has come back after a period of improvement (recurrent) and has spread from where it first started (primary site) to other places in the body (metastatic). Standard prostate cancer treatment decreases hormone levels, specifically estrogen, in the body which can lead to hot flashes, fatigue, decreased bone health, and cardiovascular and metabolic dysfunction. Transdermal estrogen may help to alleviate these symptoms. Androgen receptor signaling inhibitors work by blocking the effects of androgen (a male reproductive hormone) to stop the growth and spread of tumor cells. LHRH analogues are a type of androgen deprivation therapy that blocks the use of androgen by the tumor cells. Giving estrogen with androgen receptor signaling inhibitor may improve quality of life in men with newly diagnosed or recurrent metastatic hormone sensitive prostate cancer.
Trial Details
NCT Number NCT07466498
Lead Sponsor Fred Hutchinson Cancer Center
Collaborators: Institute for Prostate Cancer Research (IPCR)
Conditions Castration-Sensitive Prostate Adenocarcinoma, Metastatic Castration-Sensitive Prostate Adenocarcinoma, Stage IVB Prostate Cancer AJCC v8
Enrollment 60 participants
Start Date 2026-11-01
Primary Completion 2029-06-01 (estimated)
Study Completion 2029-06-01 (estimated)
Updated on ClinicalTrials.gov 2026-08-31