A Pre-Op Window Study Evaluating Anti-Proliferative Effects of Atorvastatin on the Endometrium

EARLY_PHASE1CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

November 30, 2015

Primary Completion Date

September 26, 2019

Study Completion Date

September 26, 2019

Conditions
Endometrial Cancer
Interventions
DRUG

Atorvastatin

Once enrolled on this pre-operative window study, patients with endometrial cancer will be treated with the standard clinical dose of atorvastatin (80 mg once daily orally) for an average of 2-4 weeks prior to surgical staging. Patients will need to be able to undergo atorvastatin treatment for a minimum of 2 weeks but no more than a maximum of 4 weeks prior to surgical staging.

Trial Locations (1)

27599

University of North Carolina at Chapel Hill Lineberger Comprehensive Cancer Center, Chapel Hill

All Listed Sponsors
collaborator

Wilma Williams Education and Clinical Research for Endometrial Cancer Award

UNKNOWN

lead

UNC Lineberger Comprehensive Cancer Center

OTHER

NCT02767362 - A Pre-Op Window Study Evaluating Anti-Proliferative Effects of Atorvastatin on the Endometrium | Biotech Hunter | Biotech Hunter