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NCT00010192 · ClinicalTrials.gov registry record · Phase 1

Rituximab Plus Interleukin-2 in Treating Patients With Hematologic Cancer

A Phase 1 study, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 1
Development phase
30
Enrollment target

NCT00010192: Completed Phase 1 study, sponsored by National Cancer Institute (NCI).

NCT00010192 is a Phase 1 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 30 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00010192, a Phase 1 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 1
Development phase
30 participants
Enrollment target

Study Summary

Monoclonal antibodies such as rituximab can locate cancer cells and either kill them or deliver cancer-killing substances to them without harming normal cells. Interleukin-2 may stimulate a person's white blood cells to kill cancer cells. Combining rituximab with interleukin-2 may kill more cancer cells. Phase I trial to study the effectiveness of rituximab plus interleukin-2 in treating patients who have hematologic cancer.

Primary Outcome

Data collected will be descriptive and provide limited estimates of variability given the small sample sizes at each dose level.

Interventions

  • OTHER laboratory biomarker analysis
  • BIOLOGICAL rituximab
  • OTHER pharmacological study
  • BIOLOGICAL aldesleukin

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2000-12
Phase Phase 1
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT00010192 record still lists

NCT00010192 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower).

The record links to 0 conditions, and to 4 interventions - of which laboratory biomarker analysis is the first listed.

NCT00010192 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00010192 about?

NCT00010192 is a clinical study titled "Rituximab Plus Interleukin-2 in Treating Patients With Hematologic Cancer". Monoclonal antibodies such as rituximab can locate cancer cells and either kill them or deliver cancer-killing substances to them without harming normal cells. Interleukin-2 may stimulate a person's white blood cells to kill cancer cells. Combining rituximab with interleukin-2 may kill more cancer c...

What is the current status of trial NCT00010192?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2000-12.

What interventions are being tested in trial NCT00010192?

The interventions under investigation include: laboratory biomarker analysis (OTHER), rituximab (BIOLOGICAL), pharmacological study (OTHER), aldesleukin (BIOLOGICAL).

Who is sponsoring clinical trial NCT00010192?

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

How this trial's enrollment target compares

Where NCT00010192's enrollment target sits among peer trials

30 1332nd of 2000 higher than 561 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00010192, the US trial registry maintained by the National Library of Medicine. NCT00010192 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.