Randomized, multicentre, prospective, two-arm, open-label Phase II study to investigate the efficacy and safety of two ZK219477 i.v. infusions (3-hour infusion of 16mg/m2 versus 0.5-hour infusion of 16mg/m2) in patients with recurrent ovarian cancer progressing during, or within 6 months of the end of platinum-based chemotherapy

Registry ID
EUCTR2005-000635-15
Source registry
EUCTR
Status
Completed
Phase
PHASE2
Sponsor
Schering AG
Start date
2005-07-06
Completion date
2007-06-26
Last update
2026-08-16

Conditions

Summary

To investigate the efficacy of ZK 219477 in patients with recurrent ovarian cancer progressing during, or within 6 months of platinum-based chemotherapy (proof of concept)

Locations

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