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NCT00005601 · ClinicalTrials.gov registry record · Phase 2

Combination Chemotherapy Plus Rituximab in Treating Patients With Relapsed Non-Hodgkin's Lymphoma

A Phase 2 study, sponsored by Alliance for Clinical Trials in Oncology.

Completed
Registry status
Phase 2
Development phase
58
Enrollment target

NCT00005601: Completed Phase 2 study, sponsored by Alliance for Clinical Trials in Oncology.

NCT00005601 is a Phase 2 study that has completed, run by Alliance for Clinical Trials in Oncology. The registered enrollment target is 58 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (56% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00005601, a Phase 2 study, has completed, sponsored by Alliance for Clinical Trials in Oncology.

COMPLETED
Registry status
Phase 2
Development phase
58 participants
Enrollment target

Study Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Monoclonal antibodies, such as rituximab, can locate cancer cells and either kill them or deliver cancer-killing substances to them without harming normal cells. Combining combination chemotherapy with monoclonal antibody therapy may kill more cancer cells. PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy plus rituximab in treating patients who have relapsed non-Hodgkin's lymphoma.

Interventions

  • DRUG cisplatin
  • BIOLOGICAL rituximab
  • DRUG dexamethasone
  • DRUG cytarabine
  • DRUG sargramostim

Trial Details

FieldValue
Enrollment Target 58 participants
Start Date 2000-10
Est. Completion 2008-02
Phase Phase 2

What the finished NCT00005601 record still lists

NCT00005601 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 58 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (56% lower).

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

NCT00005601 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00005601 about?

NCT00005601 is a clinical study titled "Combination Chemotherapy Plus Rituximab in Treating Patients With Relapsed Non-Hodgkin's Lymphoma". RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Monoclonal antibodies, such as rituximab, can locate cancer cells and either kill them or deliver cancer-killing substances to them without harming normal cells. Combining combina...

What is the current status of trial NCT00005601?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 58 participants. The study started on 2000-10. Estimated completion is 2008-02.

What interventions are being tested in trial NCT00005601?

The interventions under investigation include: cisplatin (DRUG), rituximab (BIOLOGICAL), dexamethasone (DRUG), cytarabine (DRUG), sargramostim (DRUG).

Who is sponsoring clinical trial NCT00005601?

This trial is sponsored by Alliance for Clinical Trials in Oncology, which has 446 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00005601's enrollment target sits among peer trials

58 1135th of 2000 higher than 860 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00005601, the US trial registry maintained by the National Library of Medicine. NCT00005601 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.