Last updated: 11/07/2018 00:54:18
A Phase II, Multicentre, Open Label Study of Oral Topotecan and Cisplatin in Ovarian Cancer Recurring ≥6 Months Following Initial Platinum-based Chemotherapy
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A Phase II, Multicentre, Open Label Study of Oral Topotecan and Cisplatin in Ovarian Cancer Recurring ≥6 Months Following Initial Platinum-based Chemotherapy
Trial description: A Phase II, Multicentre, Open Label Study of Oral Topotecan and Cisplatin in Ovarian Cancer Recurring ≥6 Months Following Initial Platinum-based Chemotherapy
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Jasas K; Trudeau M; Stuart G; Gillesby B; Fields N; Oza A: Early results of a phase II study of oral topotecan and intravenous cisplatin in epithelial ovarian cancer recurring more than 6 months following initial platinum therapy. European Journal of Cancer Supplements; Vol. 1, No. 5, September 2003, page S59: (Abstract 185)
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
2003-19-12
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
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