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Completed Phase 3 Interventional

Epoetin Alfa in Treating Anemia in Patients With Lymphoma, Chronic Lymphocytic Leukemia, or Multiple Myeloma and Anemia Caused By Chemotherapy

ClinicalTrials.gov ID: NCT00003341

Public ClinicalTrials.gov record NCT00003341. 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, 8:34 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

The Effects of Procrit (Epoetin Alfa) on Hemoglobin Symptom Distress and Quality of Life During Chemotherapy in Lymphoma Patients With Mild to Moderate Anemia A Multicenter Trial

Study identification

NCT ID
NCT00003341
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Memorial Sloan Kettering Cancer Center
Other
Enrollment
275 participants

Conditions and interventions

Interventions

  • epoetin alfa Biological
  • quality-of-life assessment Procedure

Biological · Procedure

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
Nov 30, 1997
Primary completion
Aug 31, 2003
Completion
Aug 31, 2003
Last update posted
Jul 2, 2013

1997 – 2003

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Alta Bates Comprehensive Cancer Center Berkeley California 94704
USC/Norris Comprehensive Cancer Center and Hospital Los Angeles California 90033-0804
Jonsson Comprehensive Cancer Center, UCLA Los Angeles California 90095-1781
Comprehensive Cancer Centers of the Desert Palm Springs California 92262
Division of Oncology Palo Alto California 94304
George Washington University Medical Center Washington D.C. District of Columbia 20037
H. Lee Moffitt Cancer Center and Research Institute Tampa Florida 33612-9497
Rush Cancer Institute Chicago Illinois 60612
University of Chicago Cancer Research Center Chicago Illinois 60637-1470
Marlene & Stewart Greenebaum Cancer Center, University of Maryland Baltimore Maryland 21201
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
Roswell Park Cancer Institute Buffalo New York 14263-0001
Memorial Sloan-Kettering Cancer Center New York New York 10021
Duke Comprehensive Cancer Center Durham North Carolina 27710
Cleveland Clinic Taussig Cancer Center Cleveland Ohio 44195
Milton S. Hershey Medical Center Hershey Pennsylvania 17033-0850
Vanderbilt-Ingram Cancer Center Nashville Tennessee 37232-6838
University of Texas - MD Anderson Cancer Center Houston Texas 77030-4009

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 NCT00003341, 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 Jul 2, 2013 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00003341 live on ClinicalTrials.gov.

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