A Study of Giredestrant in Participants With Grade 1 Endometrial Cancer

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

June 27, 2023

Primary Completion Date

June 30, 2026

Study Completion Date

June 30, 2026

Conditions
Endometrial Cancer
Interventions
DRUG

Giredestrant

Participants will receive giredestrant 30 milligrams (mg) taken orally (PO) once a day (QD) on Days 1 to 28 of each 28-day cycle for 6 cycles. After completion of 6 cycles, the participant and investigator can choose to continue study treatment for an additional 18 cycles or discontinue study treatment and receive investigator-determined care.

Trial Locations (12)

15224

Western Pennsylvania Hospital, Pittsburgh

23502

Virginia Oncology Associates, Norfolk

33140

Mount Sinai Medical Center, Miami Beach

47014

Istituto Scientifico Romagnolo Per Lo Studio E La Cura Dei Tumori IRST - PPDS, Meldola

55404

Minnesota Oncology Minneapolis, Minneapolis

72205

University of Arkansas for Medical Sciences, Little Rock

76104

Texas Oncology, P.A. - Fort Worth, Fort Worth

07631

Englewood Health/Hematology Oncology Practice of Englewood (HOPE), Englewood

H3T 1E2

Jewish General Hospital, Montreal

H4A 3J1

McGill University Health Centre - Glen Site, Montreal

44-101

Narodowy Inst.Onkol.im.Sklodowskiej-Curie Panstw.Inst.Bad Gliwice, Gliwice

25-734

Swietokrzyskie Centrum Onkologii, Kielce

All Listed Sponsors
lead

Hoffmann-La Roche

INDUSTRY