Fatty Acid Synthase Inhibition in Castration Refractory Prostate Cancer

PHASE2RecruitingINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

March 5, 2021

Primary Completion Date

January 31, 2026

Study Completion Date

April 30, 2028

Conditions
Prostate CancerRefractory CancerCastration Resistant Prostatic Cancer
Interventions
DRUG

Omeprazole 80 mg twice daily

Participants will be treated with omeprazole 80 mg twice daily on Day 0. Within 10 days of starting omeprazole, participants will be treated with standard prostate cancer dosing of every three week docetaxel or cabazitaxel based on package insert. Participants that have only had docetaxel will be retreated with docetaxel along with concurrent omeprazole. Patients that have had both docetaxel and cabazitaxel will be retreated with either cabazitaxel or docetaxel (investigators choice) along with concurrent omeprazole. However investigators encourage investigator to choose cabazitaxel in patients previously treated with cabazitaxel.

Trial Locations (2)

27157

RECRUITING

Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem

28144

RECRUITING

W.G. Bill Hefner VA Medical Center, Salisbury

All Listed Sponsors
collaborator

National Cancer Institute (NCI)

NIH

lead

Wake Forest University Health Sciences

OTHER

NCT04337580 - Fatty Acid Synthase Inhibition in Castration Refractory Prostate Cancer | Biotech Hunter | Biotech Hunter