ARIEL4: A Study of Rucaparib Versus Chemotherapy BRCA Mutant Ovarian, Fallopian Tube, or Primary Peritoneal Cancer Patients identifier:
NCT02855944 (

Study Contact Information:

Questions about the study should be directed to Clovis Oncology Clinical Trial Navigation Service at: 1-855-262-3040

The study is open and recruiting at sites in these state: AZ, CA, CO, FL, ME, MI, NY, OH and these countries: Canada, Czechia, Brazil, Hungary, Israel, Italy, Poland, Spain, Ukraine, United Kingdom

About the Study

ARIEL4 is a treatment study for women with relapsed, high-grade epithelial ovarian, fallopian tube, or primary peritoneal cancer who have a BRCA1 or BRCA2 mutation. ARIEL4 is designed to evaluate rucaparib against standard of care chemotherapy in women who have had at least two prior chemotherapy regimens. 


Type of Study

ARIEL4 is a randomized, 2-arm, open-label cross-over study. 

What the Study Entails

Patient who qualify for the ARIEL4 trial and enroll, receive the following as part of the study: standard-of-care and study related clinical exams, blood tests, imaging scans of your cancer, lab test results including BRCA and the other biomarker tests, the study medication (rucaparib or chemotherapy) and other assessments. Patients who were treated with chemotherapy on the main study and then experience a worsening of their ovarian cancer may be eligible to receive rucaparib after they discontinue chemotherapy.

Study Sites

Study sites are open in several states in the US and international sites are open as well. 

US Sites:

State City Facility Contact Info
Arizona Tucson University of Arizona cancer CenteAllison Wolgast (Study Coordinator) by phone: 1-313-576-8994 or by emailr Yrma Burruel (Study Coordinator) by phone: 1-520-694-9081l
Elizabeth (Jennie) Collins (Study Coordinator) by phone: 1-520-694-9067
California Monterey Pacific Cancer Care Leslie Hohenbrink (Study Coordinator) by phone: 1-831-375-4105
Orange University of California Irvine Health Chao Family Comprehensive Cancer Center Anita Wallick (Study Coordinator) by phone: 1-714-456-6191
Colorado Littleton Rocky Mountain Cancer Center Valerie Apodaca by phone: 1-303-285-5081 
Florida Orlando Florida Hospital Cancer Institute Jane LeBlanc (Study Coordinator) by phone: 1-407-303-2090, ext: 1104286
Maine Scarborough Maine Medical Center Maine Medical Partners Gynecologic Oncology Robin Donovan (Study Coordinator) by phone: 1-207-396-7089
Michigan Detroit Wayne State University Allison Wolgast (Study Coordinator) by phone: 1-313-576-8994
New York Mineola Women's Contemporary Care Associates (WCCA) – Mineola Jennifer Brown (Study Coordinator) by phone: 1-516-663-3115 or
Ohio Cincinnati University of Cincinnati Lisa Woeste (Study Coordinator) by phone: 1-513-584-4528

International Study Sites:

Canada, Czechia, Brazil, Hungary, Israel, Italy, Poland, Spain, Ukraine, United Kingdom

This Study is Open To:


This Study is Not Open To:


FORCE is a national nonprofit organization, established in 1999. Our mission is to improve the lives of individuals and families affected by adult hereditary cancers.