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NOT YET RECRUITING
NCT06129851
PHASE2

Relugolix in Combination With Radiation Therapy for Treating Patients With High Risk Prostate Cancer

Sponsor: University of Kansas Medical Center

View on ClinicalTrials.gov

Summary

This phase II trial evaluates the best duration for relugolix to be given in combination with radiation therapy when treating patients with high risk prostate cancer. Prostate cancer is a hormonal influenced cancer. Part of the usual treatment for patients with prostate cancer is androgen deprivation therapy (ADT). ADT is used to lower the amount of testosterone in the body, because testosterone appears to help prostate cancer grow. Relugolix works to reduce testosterone levels, which may inhibit proliferation of prostate cancer cells. It is approved by the Food and Drug Administration to treat prostate cancer. Adding relugolix to standard radiation therapy might work better and have fewer side effects than prior forms of hormonal therapy, but the optimal duration of relugolix in combination with radiation is not known.

Official title: Quantifying Optimal Relugolix Duration With Radiation in High Risk Prostate Cancer (QURE-PC)

Key Details

Gender

MALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

90

Start Date

2023-11-20

Completion Date

2026-10-23

Last Updated

2023-11-13

Healthy Volunteers

No

Interventions

PROCEDURE

Biospecimen Collection

Undergo blood sample collection

PROCEDURE

Bone Scan

Undergo bone scan

RADIATION

Brachytherapy

Undergo brachytherapy

PROCEDURE

Computed Tomography

Undergo CT

PROCEDURE

Dual X-ray Absorptiometry

Undergo DEXA scan

RADIATION

External Beam Radiation Therapy

Undergo external beam radiation therapy

PROCEDURE

Magnetic Resonance Imaging

Undergo MRI

PROCEDURE

PSMA PET Scan

Undergo PSMA PET

OTHER

Questionnaire Administration

Ancillary studies

DRUG

Relugolix

Given PO

Locations (1)

University of Kansas Cancer Center

Kansas City, Kansas, United States