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Brief Title: Olaparib Treatment in Relapsed Germline Breast Cancer Susceptibility Gene (BRCA) Mutated Ovarian Cancer Patients Who Have Progressed at Least 6 Months After Last Platinum Treatment and Have Received at Least 2 Prior Platinum Treatments
Official Title: A Phase III, Open Label, Randomised, Controlled, Multi-centre Study to Assess the Efficacy and Safety of Olaparib Monotherapy Versus Physician's Choice Single Agent Chemotherapy in the Treatment of Platinum Sensitive Relapsed Ovarian Cancer in Patients Carrying Germline BRCA1/2 Mutations.
Study ID: NCT02282020
Brief Summary: Comparison of olaparib vs. physician's choice of single agent standard of care non-platinum based chemotherapy in patients with germline Breast Cancer susceptibility gene (gBRCA) mutated ovarian cancer who have progressed at least 6 months after the last platinum based chemotherapy. Patient should have received at least 2 prior lines of platinum based chemotherapy. The aim of the study is to assess the efficacy and safety of olaparib tablets.
Detailed Description: This open label, randomised, controlled, multi-centre study will assess the efficacy and safety of single agent olaparib vs. standard of care, based on physician's choice of single agent chemotherapy ( i.e paclitaxel, or topotecan, or pegylated liposomal doxorubicin, or gemcitabine) in platinum sensitive or partially platinum sensitive relapsed ovarian cancer patients who carry germline deleterious or suspected deleterious BRCA mutation and who have received at least 2 prior lines of platinum based chemotherapy. Patients are eligible to undergo BRCA testing even if they have not yet had recurrence or progression of disease \>6 months (\>/=183 days) after completion of their last platinum therapy.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: FEMALE
Healthy Volunteers: No
Research Site, Birmingham, Alabama, United States
Research Site, Mobile, Alabama, United States
Research Site, Sacramento, California, United States
Research Site, San Francisco, California, United States
Research Site, Aurora, Colorado, United States
Research Site, Littleton, Colorado, United States
Research Site, Hartford, Connecticut, United States
Research Site, Fort Gordon, Georgia, United States
Research Site, Covington, Louisiana, United States
Research Site, Towson, Maryland, United States
Research Site, Detroit, Michigan, United States
Research Site, Albany, New York, United States
Research Site, Mineola, New York, United States
Research Site, Chapel Hill, North Carolina, United States
Research Site, Columbus, Ohio, United States
Research Site, Springfield, Oregon, United States
Research Site, Abington, Pennsylvania, United States
Research Site, Knoxville, Tennessee, United States
Research Site, Nashville, Tennessee, United States
Research Site, Bedford, Texas, United States
Research Site, Houston, Texas, United States
Research Site, Milwaukee, Wisconsin, United States
Research Site, Berazategui, , Argentina
Research Site, Caba, , Argentina
Research Site, Ciudad de Buenos Aires, , Argentina
Research Site, Cordoba, , Argentina
Research Site, La Plata, , Argentina
Research Site, San Miguel de Tucumán, , Argentina
Research Site, Gent, , Belgium
Research Site, Leuven, , Belgium
Research Site, Ijui, , Brazil
Research Site, Passo Fundo, , Brazil
Research Site, Porto Alegre, , Brazil
Research Site, Porto Alegre, , Brazil
Research Site, Rio de Janeiro, , Brazil
Research Site, Sao Paulo, , Brazil
Research Site, Sao Paulo, , Brazil
Research Site, São José do Rio Preto, , Brazil
Research Site, Toronto, Ontario, Canada
Research Site, Toronto, Ontario, Canada
Research Site, Montreal, Quebec, Canada
Research Site, Hradec Kralove, , Czechia
Research Site, Ostrava-Poruba, , Czechia
Research Site, Praha 2, , Czechia
Research Site, Zlin, , Czechia
Research Site, Budapest, , Hungary
Research Site, Budapest, , Hungary
Research Site, Budapest, , Hungary
Research Site, Debrecen, , Hungary
Research Site, Győr, , Hungary
Research Site, Miskolc, , Hungary
Research Site, Afula, , Israel
Research Site, Haifa, , Israel
Research Site, Holon, , Israel
Research Site, Jerusalem, , Israel
Research Site, Jerusalem, , Israel
Research Site, Petah Tikva, , Israel
Research Site, Ramat Gan, , Israel
Research Site, Rehovot, , Israel
Research Site, Tel Hashomer, , Israel
Research Site, Tel-Aviv, , Israel
Research Site, Zerifin, , Israel
Research Site, Meldola, , Italy
Research Site, Messina, , Italy
Research Site, Milano, , Italy
Research Site, Milano, , Italy
Research Site, Milano, , Italy
Research Site, Napoli, , Italy
Research Site, Roma, , Italy
Research Site, Roma, , Italy
Research Site, Goyang-si, , Korea, Republic of
Research Site, Seoul, , Korea, Republic of
Research Site, Seoul, , Korea, Republic of
Research Site, Seoul, , Korea, Republic of
Research Site, Seoul, , Korea, Republic of
Research Site, Seoul, , Korea, Republic of
Research Site, Mexico, , Mexico
Research Site, Mexico, , Mexico
Research Site, Oaxaca, , Mexico
Research Site, Gdańsk, , Poland
Research Site, Grzepnica, , Poland
Research Site, Lublin, , Poland
Research Site, Olsztyn, , Poland
Research Site, Poznan, , Poland
Research Site, Warszawa, , Poland
Research Site, Łódź, , Poland
Research Site, Barcelona, , Spain
Research Site, Barcelona, , Spain
Research Site, Barcelona, , Spain
Research Site, Córdoba, , Spain
Research Site, Gerona, , Spain
Research Site, Granada, , Spain
Research Site, Madrid, , Spain
Research Site, Madrid, , Spain
Name: Richard T Penson, Associate Prof. of Medicine
Affiliation: Harvard Medical School (HMS and HSDM)
Role: PRINCIPAL_INVESTIGATOR