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NCT00541034 · ClinicalTrials.gov registry record · Phase 2

Pentostatin, Cyclophosphamide, and Rituximab in Treating Patients With Previously Untreated Chronic Lymphocytic Leukemia

A Phase 2 study, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
Phase 2
Development phase
49
Enrollment target

NCT00541034: Completed Phase 2 study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT00541034 is a Phase 2 study that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 49 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00541034, a Phase 2 study, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
49 participants
Enrollment target

Study Summary

RATIONALE: Pentostatin may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as cyclophosphamide, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as rituximab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. Giving pentostatin together with cyclophosphamide and rituximab may kill more cancer cells. PURPOSE: This phase II trial is studying the side effects and how well giving pentostatin together with cyclophosphamide and rituximab works in treating patients with previously untreated chronic lymphocytic leukemia.

Interventions

  • DRUG cyclophosphamide
  • BIOLOGICAL rituximab
  • DRUG pentostatin

Trial Details

FieldValue
Enrollment Target 49 participants
Start Date 2005-05
Est. Completion 2016-01
Phase Phase 2

Sponsor

Memorial Sloan Kettering Cancer Center

1,884 total trials

What the Registry Record Tells You About NCT00541034

The ClinicalTrials.gov registry entry for NCT00541034 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 49 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 1,884 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which cyclophosphamide is the first listed.

NCT00541034 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00541034 about?

NCT00541034 is a clinical study titled "Pentostatin, Cyclophosphamide, and Rituximab in Treating Patients With Previously Untreated Chronic Lymphocytic Leukemia". RATIONALE: Pentostatin may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as cyclophosphamide, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Monoclona...

What is the current status of trial NCT00541034?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 49 participants. The study started on 2005-05. Estimated completion is 2016-01.

What interventions are being tested in trial NCT00541034?

The interventions under investigation include: cyclophosphamide (DRUG), rituximab (BIOLOGICAL), pentostatin (DRUG).

Who is sponsoring clinical trial NCT00541034?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 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.