D8488C00001/ CONCERTO: A single arm, open-label, Phase IIb study to assess the efficacy and safety of the combination of cediranib and olaparib tablets in women with recurrent platinum resistant epithelial ovarian cancer, including Fallopian tube and/or primaryperitoneal cancer who do not carry a deleterious or suspected deleterious germline BRCA mutation
CONCERTO: Study of combination tablets in women with recurrent platinum resistant epithelian ovarian cancer
Sponsor: AstraZeneca
Enrolling: Female Patients Only
IRB Number: AAAR5554
U.S. Govt. ID: NCT02889900
Contact: Reena Vattakalam: 212-342-6895 / rmv2110@cumc.columbia.edu
Additional Study Information: A single arm, open-label, Phase IIb study to assess the efficacy and safety of the combination of cediranib and olaparib tablets in women with recurrent platinum resistant epithelial ovarian cancer, including Fallopian tube and/or primary peritoneal cancer who do not carry a deleterious or suspected deleterious germline BRCA mutation. The purpose of the study is to see if the combination of two drugs, cediranib and olaparib, is effective and tolerable in patients with ovarian cancer who have received at least 3 prior chemotherapy treatments, including treatment that included either carboplatin or cisplatin, and their disease came back within 6 months of the last dose of chemotherapy that included either cisplatin or carboplatin.
This study is closed
Investigator
Jason Wright, MD
Do You Qualify?
Have you been diagnosed with endometroid, ovarian cancer, fallopian tube or primary peritoneal carcinoma? Yes No
Have you been found to have BRCA1 or BRCA2 gene mutations? Yes No
Have you had at least 3 previous chemotherapy lines? Yes No
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You may be eligible for this study

Place Holder




For more information, please contact:
Reena Vattakalam
rmv2110@cumc.columbia.edu
212-342-6895