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NCT00002565 · ClinicalTrials.gov registry record · Phase 3

Combination Chemotherapy in Treating Patients With Intermediate-Grade or Immunoblastic Non-Hodgkin's Lymphoma

A Phase 3 study of Lymphoma, sponsored by M.D. Anderson Cancer Center.

Completed
Registry status
Phase 3
Development phase
61
Enrollment target
3
Study locations

NCT00002565 is a Phase 3 study of Lymphoma that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 61 participants, below the 484-participant average among 299 other Lymphoma trials with a reported enrollment target (87% lower). The trial reports 3 study locations across 2 states.

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The verdict

NCT00002565, a Phase 3 study of Lymphoma, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
Phase 3
Development phase
61 participants
Enrollment target
3
Study locations

Study Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Combining more than one drug may kill more cancer cells. It is not yet known which combination chemotherapy regimen is more effective for intermediate-grade or immunoblastic non-Hodgkin's lymphoma. PURPOSE: Randomized phase III trial to compare the effectiveness of two combination chemotherapy regimens in treating patients who have intermediate-grade or immunoblastic non-Hodgkin's lymphoma.

Conditions Studied

Interventions

  • DRUG cisplatin
  • DRUG cyclophosphamide
  • DRUG cytarabine
  • DRUG CHOP regimen
  • BIOLOGICAL bleomycin sulfate

Study Locations (3)

Other

  • Faculdade de Medicina do ABC - São Paulo
  • Clinica Alemana - Santiago

Texas

  • University of Texas - MD Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 61 participants
Start Date 1994-05-25
Est. Completion 2007-02-05
Phase Phase 3

Sponsor

M.D. Anderson Cancer Center

2,692 total trials

What the Registry Record Tells You About NCT00002565

The ClinicalTrials.gov registry entry for NCT00002565 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 61 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 484-participant average among 299 other Lymphoma trials with a reported enrollment target (87% lower). The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Lymphoma appearing as the primary indexed condition, and to 5 interventions - of which cisplatin is the first listed.

NCT00002565 reports 3 study locations spanning 2 distinct geographic areas - top geographies include Other, Texas.

Frequently Asked Questions

What is clinical trial NCT00002565 about?

NCT00002565 is a clinical study titled "Combination Chemotherapy in Treating Patients With Intermediate-Grade or Immunoblastic Non-Hodgkin's Lymphoma". RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Combining more than one drug may kill more cancer cells. It is not yet known which combination chemotherapy regimen is more effective for intermediate-grade or immunoblastic non-H...

What is the current status of trial NCT00002565?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 61 participants. The study started on 1994-05-25. Estimated completion is 2007-02-05.

What conditions does trial NCT00002565 study?

This clinical trial studies the following conditions: Lymphoma.

What interventions are being tested in trial NCT00002565?

The interventions under investigation include: cisplatin (DRUG), cyclophosphamide (DRUG), cytarabine (DRUG), CHOP regimen (DRUG), bleomycin sulfate (BIOLOGICAL).

Who is sponsoring clinical trial NCT00002565?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00002565 being conducted?

This trial has 3 study locations across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.