ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Dose-Adjusted EPOCH Chemotherapy and Rituximab (CD20+) in Previously Untreated Aggressive Non-Hodgkin's Lymphoma

ClinicalTrials.gov ID: NCT00001337

Public ClinicalTrials.gov record NCT00001337. 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 May 18, 2026, 1:42 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

Dose-Adjusted EPOCH Chemotherapy and Rituximab (CD20+) in Adults and Children With Previously Untreated Patients With Aggressive Non-Hodgkin's Lymphoma

Study identification

NCT ID
NCT00001337
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
National Cancer Institute (NCI)
NIH
Enrollment
348 participants

Conditions and interventions

Interventions

  • Biopsy Procedure
  • CT Diagnostic Test
  • Cyclophosphamide Drug
  • Docusate Sodium + Sennosides Other
  • Doxorubicin Drug
  • Etoposide Drug
  • Lactulose Other
  • Laparotomy Procedure
  • MRI Diagnostic Test
  • Omeprazole Other
  • Ondansetron Other
  • PET scan Diagnostic Test
  • Prednisone Drug
  • Prochlorperazine Other
  • Rituximab Biological
  • Vincristine Drug

Procedure · Diagnostic Test · Drug + 2 more

Eligibility (public fields only)

Age range
12 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 7, 1993
Primary completion
May 23, 2024
Completion
May 23, 2024
Last update posted
Jun 21, 2025

1993 – 2024

United States locations

U.S. sites
5
U.S. states
4
U.S. cities
5
Facility City State ZIP Site status
Holy Cross Hospital, Fort Lauderdale Fort Lauderdale Florida 33308
University of Maryland, Baltimore Baltimore Maryland 21201-1595
National Institutes of Health Clinical Center Bethesda Maryland 20892
Brigham and Women's Hospital Boston Massachusetts 02115
St. Luke's Roosevelt Hospital New York New York 10025

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 NCT00001337, 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 21, 2025 · Synced May 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00001337 live on ClinicalTrials.gov.

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