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NCT00061308 · ClinicalTrials.gov registry record · Phase 2

Second-line Intravenous Treatment For Recurrent Platinum-Sensitive Ovarian, Fallopian, Or Peritoneal Cancer

A Phase 2 study, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 2
Development phase
75
Enrollment target

NCT00061308: Completed Phase 2 study, sponsored by GlaxoSmithKline.

NCT00061308 is a Phase 2 study that has completed, run by GlaxoSmithKline. The registered enrollment target is 75 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (44% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00061308, a Phase 2 study, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
Phase 2
Development phase
75 participants
Enrollment target

Study Summary

This research study was designed to determine the effectiveness of the drug, topotecan, given intravenously (into a vein) together with the drug gemcitabine in patients with recurrent platinum-sensitive ovarian, fallopian or primary peritoneal cancer, as well as tumors of mixed mullerian origin. Additional purposes are to determine the long term outcome and side effects of this combination treatment. Since topotecan and gemcitabine have different mechanisms of action, the combination of these 2 drugs may provide better results than either drug alone. Prior studies suggest that the combination of topotecan and gemcitabine improves the effects on the tumor and also appeared to be well tolerated.

Interventions

  • DRUG Gemcitabine
  • DRUG Topotecan

Trial Details

FieldValue
Enrollment Target 75 participants
Start Date 2002-12
Phase Phase 2
GlaxoSmithKline

1,345 total trials

What the finished NCT00061308 record still lists

NCT00061308 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 75 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (44% lower).

The record links to 0 conditions, and to 2 interventions - of which Gemcitabine is the first listed.

NCT00061308 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00061308 about?

NCT00061308 is a clinical study titled "Second-line Intravenous Treatment For Recurrent Platinum-Sensitive Ovarian, Fallopian, Or Peritoneal Cancer". This research study was designed to determine the effectiveness of the drug, topotecan, given intravenously (into a vein) together with the drug gemcitabine in patients with recurrent platinum-sensitive ovarian, fallopian or primary peritoneal cancer, as well as tumors of mixed mullerian origin. Add...

What is the current status of trial NCT00061308?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 75 participants. The study started on 2002-12.

What interventions are being tested in trial NCT00061308?

The interventions under investigation include: Gemcitabine (DRUG), Topotecan (DRUG).

Who is sponsoring clinical trial NCT00061308?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00061308's enrollment target sits among peer trials

75 900th of 2000 higher than 1,081 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00061308, the US trial registry maintained by the National Library of Medicine. NCT00061308 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.