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NCT00001337 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 2
Development phase
348
Enrollment target

NCT00001337: Completed Phase 2 study, sponsored by National Cancer Institute (NCI).

NCT00001337 is a Phase 2 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 348 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00001337, a Phase 2 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 2
Development phase
348 participants
Enrollment target

Study Summary

5-Drug Combination Chemotherapy with Hematologic Toxicity Attenuation. Etoposide phosphate, prednisone, vincristine sulfate (Oncovin), cyclophosphamide, and doxorubicin hydrochloride (hydroxydaunorubicin)(EPOCH): Etoposide, VP-16, NSC-141540; Prednisone, PRED, NSC-10023; Vincristine, VCR, NSC-67574; Cyclophosphamide, CTX, NSC-26271; Doxorubicin, DOX, NSC-123127; with Granulocyte Colony-Stimulating Factor (Amgen), Granulocyte colony-stimulating factor (G-CSF), NSC-614629.

Interventions

  • DRUG Cyclophosphamide
  • DRUG Etoposide
  • DRUG Vincristine
  • DRUG Prednisone
  • BIOLOGICAL Rituximab

Trial Details

FieldValue
Enrollment Target 348 participants
Start Date 1993-05-08
Est. Completion 2024-05-24
Phase Phase 2

Sponsor

National Cancer Institute (NCI)

3,257 total trials

What the Registry Record Tells You About NCT00001337

The ClinicalTrials.gov registry entry for NCT00001337 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 348 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Cancer Institute (NCI), which has 3,257 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 5 interventions - of which Cyclophosphamide is the first listed.

NCT00001337 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00001337 about?

NCT00001337 is a clinical study titled "Dose-Adjusted EPOCH Chemotherapy and Rituximab (CD20+) in Previously Untreated Aggressive Non-Hodgkin's Lymphoma". 5-Drug Combination Chemotherapy with Hematologic Toxicity Attenuation. Etoposide phosphate, prednisone, vincristine sulfate (Oncovin), cyclophosphamide, and doxorubicin hydrochloride (hydroxydaunorubicin)(EPOCH): Etoposide, VP-16, NSC-141540; Prednisone, PRED, NSC-10023; Vincristine, VCR, NSC-67574;...

What is the current status of trial NCT00001337?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 348 participants. The study started on 1993-05-08. Estimated completion is 2024-05-24.

What interventions are being tested in trial NCT00001337?

The interventions under investigation include: Cyclophosphamide (DRUG), Etoposide (DRUG), Vincristine (DRUG), Prednisone (DRUG), Rituximab (BIOLOGICAL).

Who is sponsoring clinical trial NCT00001337?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

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

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, the data changelog, or report a data error.