Clinical trial

Second-line Intravenous Treatment For Recurrent Platinum-Sensitive Ovarian…

NCT00061308 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00061308
Title Second-line Intravenous Treatment For Recurrent Platinum-Sensitive Ovarian, Fallopian, Or Peritoneal Cancer
Official title An Open-label, Multicenter, Non-Comparative Phase II Study of the Combination of Intravenous Topotecan and Gemcitabine Administered Once Weekly for Three Weeks Every 28 Days as Second-line Treatment in Patients With Recurrent Platinum Sensitive Ovarian Cancer
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Peritoneal Cancer, Ovarian Cancer, Neoplasms, Ovarian, Fallopian Tube Cancer
Intervention type Drug
Interventions Topotecan, Gemcitabine
Enrollment 75
Start date Dec 1, 2002
Primary completion Sep 1, 2004
First posted May 28, 2003
Last update posted Jun 9, 2017
Countries Canada, United States

At a glance

  • 10–99 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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