Study of Birinapant in Combination With Conatumumab in Subjects With Relapsed Ovarian Cancer
Completed · Phase 1
Conditions studied: Relapsed Epithelial Ovarian Cancer, Relapsed Primary Peritoneal Cancer, Relapsed Fallopian Tube Cancer
In brief
This is a dose escalation study in female subjects with relapsed ovarian cancer (including epithelial ovarian cancer, primary peritoneal cancer, or fallopian tube cancer). Approximately 30 to 40 subjects will be administered a combination of conatumumab and birinapant. In the initial dose-escalation stage of the study, adult female subjects will receive conatumumab in combination with increasing doses of birinapant in dose-escalation cohorts to determine the MTD of birinapant when administered with a fixed dose of conatumumab. In safety expansion stage, adult female subjects will receive conatumumab in combination with birinapant at the MTD of the combination.
Key facts
- Study ID
- NCT01940172
- Run by
- TetraLogic Pharmaceuticals
- People needed
- 27
- Starts
- 2013-11-01
- Expected to finish
- 2015-12-01
- Last updated by the study team
- 2016-01-14
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
Where it is running
- TetraLogic research site — Fresno, California, United States
- TetraLogic Research Site — San Luis Obispo, California, United States
- TetraLogic Research Site — Fairway, Kansas, United States
- TetraLogic Research Site — Boston, Massachusetts, United States
- TetraLogic Research Site — Durham, North Carolina, United States
- TetraLogic Research Site — Philadelphia, Pennsylvania, United States
- TetraLogic Research Site — Philadelphia, Pennsylvania, United States
- TetraLogic Research Site — Nashville, Tennessee, United States
- TetraLogic Research Facility — Dallas, Texas, United States
Full record on ClinicalTrials.gov
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