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NCT00002559 · ClinicalTrials.gov registry record · Phase 1

Combination Chemotherapy in Treating Patients With Germ Cell Tumors That Have Not Responded to Previous Cisplatin

A Phase 1 study of Ovarian Cancer and Testicular Germ Cell Tumor, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
Phase 1
Development phase
43
Enrollment target
1
Study location

NCT00002559 is a Phase 1 study of Ovarian Cancer and Testicular Germ Cell Tumor that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 43 participants, below the 729-participant average among 322 other Ovarian Cancer trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00002559, a Phase 1 study of Ovarian Cancer and Testicular Germ Cell Tumor, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
Phase 1
Development phase
43 participants
Enrollment target
1
Study location

Study Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. PURPOSE: Phase I/II trial to study the effectiveness of combination chemotherapy consisting of paclitaxel, cisplatin, and ifosfamide in treating patients who have ovarian or testicular germ cell tumors that are refractory to platinum-containing chemotherapy.

Interventions

  • DRUG cisplatin
  • DRUG paclitaxel
  • DRUG ifosfamide
  • BIOLOGICAL filgrastim

Study Locations (1)

New York

  • Memorial Sloan-Kettering Cancer Center - New York

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 1994-01
Est. Completion 2003-01
Phase Phase 1

Sponsor

Memorial Sloan Kettering Cancer Center

1,884 total trials

What the Registry Record Tells You About NCT00002559

The ClinicalTrials.gov registry entry for NCT00002559 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 43 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 729-participant average among 322 other Ovarian Cancer trials with a reported enrollment target (94% lower). The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 1,884 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Ovarian Cancer appearing as the primary indexed condition, and to 4 interventions - of which cisplatin is the first listed.

NCT00002559 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT00002559 about?

NCT00002559 is a clinical study titled "Combination Chemotherapy in Treating Patients With Germ Cell Tumors That Have Not Responded to Previous Cisplatin". RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. PURPOSE: Phase I/II trial to study the effectiveness of combination chemotherapy consisting of paclitaxel, cisplatin, and i...

What is the current status of trial NCT00002559?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 43 participants. The study started on 1994-01. Estimated completion is 2003-01.

What conditions does trial NCT00002559 study?

This clinical trial studies the following conditions: Ovarian Cancer, Testicular Germ Cell Tumor.

What interventions are being tested in trial NCT00002559?

The interventions under investigation include: cisplatin (DRUG), paclitaxel (DRUG), ifosfamide (DRUG), filgrastim (BIOLOGICAL).

Who is sponsoring clinical trial NCT00002559?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00002559 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.