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Clinical Trial Summary

This is a Phase II, randomized, multi-centre study aiming at comparing the efficacy of Olaparib and Cediranib vs. weekly Paclitaxel in terms of progression free survival (PFS) in platinum refractory or resistant recurrent ovarian cancer.

Patients will be randomised in a 1:1:1 ratio to three treatment arms:

- Arm A: Paclitaxel 80 mg/mq every week

- Arm B: Cediranib 20 mg/day + Olaparib 600 mg / day (i.e. 300 mg BD) given every day

- Arm C: Cediranib 20 mg/day given 5 days per weeks + Olaparib 600 mg / day (i.e. 300 mg BD) given 7 days per weeks


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03314740
Study type Interventional
Source Mario Negri Institute for Pharmacological Research
Contact
Status Active, not recruiting
Phase Phase 2
Start date June 1, 2017
Completion date November 30, 2019

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