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| Trial name or title | A cross‐over bioequivalence study of intravenously administered ATI0918 and DOXIL/CAELYX in patients with ovarian cancer |
| Methods | Phase I single‐blind RCT |
| Participants | 40 women with ROC |
| Interventions | PLD (50 mg/m²) versus ATI‐0918 |
| Outcomes | Pharmaco‐equivalence outcomes |
| Starting date | Oct 2012 |
| Contact information | Karen Kuhn: kkuhn@ockham.com |
| Notes | May 2013 |
