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Terminated Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT00267007

Public ClinicalTrials.gov record NCT00267007. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 11:53 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled, Multicenter, 18 Week Pilot Study to Investigate the Neuroprotective Effect of PROCRIT (Epoetin Alfa) on the Development of Peripheral Neuropathy in Patients Receiving Combination Taxane and Platinum-Based Chemotherapy for Cancer

Study identification

NCT ID
NCT00267007
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Industry
Enrollment
32 participants

Conditions and interventions

Interventions

  • PROCRIT 40,000 IU QW Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 31, 2006
Primary completion
Jul 31, 2008
Completion
Jul 31, 2008
Last update posted
Jun 3, 2014

2006 – 2008

United States locations

U.S. sites
28
U.S. states
18
U.S. cities
28
Facility City State ZIP Site status
Not listed Mobile Alabama
Not listed Little Rock Arkansas
Not listed Alhambra California
Not listed Bakersfield California
Not listed Fullerton California
Not listed La Verne California
Not listed Long Beach California
Not listed Northridge California
Not listed Oxnard California
Not listed Santa Maria California
Not listed New Haven Connecticut
Not listed Hollywood Florida
Not listed Augusta Georgia
Not listed Joliet Illinois
Not listed Indianapolis Indiana
Not listed Lexington Kentucky
Not listed Bethesda Maryland
Not listed Detroit Michigan
Not listed Southfield Michigan
Not listed Las Vegas Nevada
Not listed Lebanon New Hampshire
Not listed Buffalo New York
Not listed Syracuse New York
Not listed Durham North Carolina
Not listed Winston-Salem North Carolina
Not listed Oklahoma City Oklahoma
Not listed Philadelphia Pennsylvania
Not listed Chattanooga Tennessee

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00267007, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 3, 2014 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00267007 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →