Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00267007 · ClinicalTrials.gov registry record · Phase 2

A Study to Investigate the Neuroprotective Effect of PROCRIT (Epoetin Alfa) Versus Placebo in Cancer Patients Who Develop Chemotherapy-induced Peripheral Neuropathy

A Phase 2 study, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C..

Terminated
Registry status
Phase 2
Development phase
32
Enrollment target

NCT00267007 is a Phase 2 study that was terminated before completion, run by Johnson & Johnson Pharmaceutical Research & Development, L.L.C.. The registered enrollment target is 32 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00267007, a Phase 2 study, was terminated before completion, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C..

TERMINATED
Registry status
Phase 2
Development phase
32 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the neuroprotective effect of PROCRIT (epoetin alfa, a glycoprotein that stimulates red blood cell production) versus placebo in patients with cancer who develop chemotherapy-induced peripheral neuropathy due to combination Taxane and Platinum-Based treatment.

Interventions

  • DRUG Placebo
  • DRUG PROCRIT 40,000 IU QW

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2006-06
Est. Completion 2008-08
Phase Phase 2

What the Registry Record Tells You About NCT00267007

The ClinicalTrials.gov registry entry for NCT00267007 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 32 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johnson & Johnson Pharmaceutical Research & Development, L.L.C., which has 102 total studies on file at ClinicalTrials.gov.

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

NCT00267007 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00267007 about?

NCT00267007 is a clinical study titled "A Study to Investigate the Neuroprotective Effect of PROCRIT (Epoetin Alfa) Versus Placebo in Cancer Patients Who Develop Chemotherapy-induced Peripheral Neuropathy". The purpose of this study is to evaluate the neuroprotective effect of PROCRIT (epoetin alfa, a glycoprotein that stimulates red blood cell production) versus placebo in patients with cancer who develop chemotherapy-induced peripheral neuropathy due to combination Taxane and Platinum-Based treatment...

What is the current status of trial NCT00267007?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 32 participants. The study started on 2006-06. Estimated completion is 2008-08.

What interventions are being tested in trial NCT00267007?

The interventions under investigation include: Placebo (DRUG), PROCRIT 40,000 IU QW (DRUG).

Who is sponsoring clinical trial NCT00267007?

This trial is sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C., which has 102 total clinical trials registered on ClinicalTrials.gov.

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.