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NCT00493467 · ClinicalTrials.gov registry record · Phase 2

Zevalin (Ibritumomab Tiuxetan) for Early Stage Indolent Lymphomas

A Phase 2 study, sponsored by M.D. Anderson Cancer Center.

Completed
Registry status
Phase 2
Development phase
31
Enrollment target

NCT00493467: Completed Phase 2 study, sponsored by M.D. Anderson Cancer Center.

NCT00493467 is a Phase 2 study that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 31 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00493467, a Phase 2 study, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
31 participants
Enrollment target

Study Summary

The goal of this clinical research study is to find out if giving (Rituxan) rituximab with 90Y (ibritumomab tiuxetan) (90 Y Zevalin®) may be effective in treating low-grade lymphoma. The safety of this combination treatment will also be studied.

Primary Outcome

ORR defined as the percentage of number of complete response (CR), complete response unconfirmed (CRu) or partial response (PR) in patients treated using International Working Group (IWG) revised response criteria for Malignant Lymphoma. ORR to therapy is evaluated after three months using radiographic and clinical parameters to assess response. CR: Complete disappearance of all detectable clinical and radiographic evidence of disease and disappearance of all disease-related symptoms. CRu: A res

Interventions

  • DRUG Rituximab
  • DRUG Ibritumomab Tiuxetan (Zevalin)

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2006-06
Est. Completion 2022-08-11
Phase Phase 2
M.D. Anderson Cancer Center

2,692 total trials

What the finished NCT00493467 record still lists

NCT00493467 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower).

The record links to 0 conditions, and to 2 interventions - of which Rituximab is the first listed.

NCT00493467 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00493467 about?

NCT00493467 is a clinical study titled "Zevalin (Ibritumomab Tiuxetan) for Early Stage Indolent Lymphomas". The goal of this clinical research study is to find out if giving (Rituxan) rituximab with 90Y (ibritumomab tiuxetan) (90 Y Zevalin®) may be effective in treating low-grade lymphoma. The safety of this combination treatment will also be studied.

What is the current status of trial NCT00493467?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 31 participants. The study started on 2006-06. Estimated completion is 2022-08-11.

What interventions are being tested in trial NCT00493467?

The interventions under investigation include: Rituximab (DRUG), Ibritumomab Tiuxetan (Zevalin) (DRUG).

Who is sponsoring clinical trial NCT00493467?

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

How this trial's enrollment target compares

Where NCT00493467's enrollment target sits among peer trials

31 1578th of 2000 higher than 419 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 NCT00493467, the US trial registry maintained by the National Library of Medicine. NCT00493467 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.