SGI-110 in Combination With Carboplatin in Ovarian Cancer
Status: | Completed |
---|---|
Conditions: | Ovarian Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 1/21/2018 |
Start Date: | September 2012 |
End Date: | August 2016 |
A Randomized, Controlled, Open-Label, Phase 2 Trial of SGI-110 and Carboplatin in Subjects With Platinum-Resistant Recurrent Ovarian Cancer
A 2-part, Phase 2 controlled, open-label, randomized study in patients with
platinum-resistant recurrent ovarian cancer. In Part 1, patients will receive SGI-110 and
carboplatin. The optimum dose will be identified in Part 1 based on safety and efficacy. In
Part 2, patients will be randomized to receive the dose identified in Part 1 plus carboplatin
or one of three treatment of choice at the discretion of the investigator. The treatment of
choice consists of topotecan, pegylated liposomal doxorubicin, or paclitaxel.
platinum-resistant recurrent ovarian cancer. In Part 1, patients will receive SGI-110 and
carboplatin. The optimum dose will be identified in Part 1 based on safety and efficacy. In
Part 2, patients will be randomized to receive the dose identified in Part 1 plus carboplatin
or one of three treatment of choice at the discretion of the investigator. The treatment of
choice consists of topotecan, pegylated liposomal doxorubicin, or paclitaxel.
Inclusion Criteria:
1. Patients who are women 18 years of age or older.
2. Patients who have histologically or cytologically confirmed recurrent high-grade
serous epithelial ovarian cancer (Grade 2 or 3), primary peritoneal carcinomatosis or
fallopian tube cancer.
3. Patients who have platinum-resistant disease (defined as having relapsed within 6
months of her last platinum-containing regimen). There is no limit on the number of
prior treatment regimens in Part 1. In Part 2, patients may have had no more than 3
prior cytotoxic treatment regimens, excluding adjuvant or maintenance therapy.
4. Patients must have had prior paclitaxel treatment.
5. Patients who have measurable disease according to RECIST v1.1 or detectable disease.
6. Patients with ECOG performance status of 0 or 1.
7. Patients with acceptable organ function.
8. Patients must be at least 3 weeks from last chemotherapy.
Exclusion Criteria:
1. Patients who have hypersensitivity to SGI-110 and/or carboplatin or other components
of these drug products.
2. Patients who have received prior therapy with any hypomethylating agents.
3. Patients who are refractory to platinum treatment i.e., progressed while on platinum
treatment.
4. Patients with abnormal left ventricular ejection fraction.
5. Patients with Grade 2 or greater neuropathy.
6. Patients with known brain metastases.
7. Patients with known history of HIV, HCV or HBV.
We found this trial at
14
sites
1376 Mowry Road
Gainesville, Florida 32610
Gainesville, Florida 32610
(352) 273-8010
University of Florida Shands Cancer Center We are the University of Florida Health Cancer Center
Click here to add this to my saved trials
University of Chicago One of the world's premier academic and research institutions, the University of...
Click here to add this to my saved trials
Inova Fairfax Hospital Inova Fairfax Hospital, Inova's flagship hospital, is an 833-bed, nationally recognized regional...
Click here to add this to my saved trials
Georgia Health Sciences University Georgia Regents University, home of the Medical College of Georgia, is...
Click here to add this to my saved trials
Click here to add this to my saved trials
Dana-Farber Cancer Institute Since it’s founding in 1947, Dana-Farber has been committed to providing adults...
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials