drugset / Trial / NCT01170650
Study for Women With Platinum Resistant Ovarian Cancer Evaluating EC145 in Combination With Doxil® (PROCEED)
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this study is to compare progression-free survival (PFS) (based upon investigator assessment using RECIST v1.1) in participants with platinum-resistant ovarian cancer who receive combination therapy with EC145 and pegylated liposomal doxorubicin (EC145+PLD) with that in participants who receive PLD and placebo.
Timeline
- Start
- 2011-04-22
- Primary completion
- 2015-05-31
- Completion
- 2015-09-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | EC20 | Diagnostic / imaging agent | — | Intravenous |
| Subject | Vintafolide | Other / unclassified | — | Intravenous |
| Background | Doxorubicin | Other / unclassified | 50 mg/m2 | — |