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NCT00233506 · ClinicalTrials.gov registry record · Phase 1

A Dose Finding Study of CpG in Patients With Chronic Lymphocytic Leukemia Who Have Been Previously Treated

A Phase 1 study, sponsored by University of Iowa.

Completed
Registry status
Phase 1
Development phase
41
Enrollment target

NCT00233506: Completed Phase 1 study, sponsored by University of Iowa.

NCT00233506 is a Phase 1 study that has completed, run by University of Iowa. The registered enrollment target is 41 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (32% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00233506, a Phase 1 study, has completed, sponsored by University of Iowa.

COMPLETED
Registry status
Phase 1
Development phase
41 participants
Enrollment target

Study Summary

* CpG has the potential to stimulate the immune system * this study will evaluate the safety of CpG given sub-q or IV * purpose is to measure biological changes in CLL cells after receiving CpG

Interventions

  • DRUG CpG 7909

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2004-07
Est. Completion 2011-06
Phase Phase 1
University of Iowa

228 total trials

What the finished NCT00233506 record still lists

NCT00233506 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 41 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (32% lower).

The record links to 0 conditions, and to 1 intervention - of which CpG 7909 is the first listed.

NCT00233506 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00233506 about?

NCT00233506 is a clinical study titled "A Dose Finding Study of CpG in Patients With Chronic Lymphocytic Leukemia Who Have Been Previously Treated". * CpG has the potential to stimulate the immune system * this study will evaluate the safety of CpG given sub-q or IV * purpose is to measure biological changes in CLL cells after receiving CpG

What is the current status of trial NCT00233506?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 41 participants. The study started on 2004-07. Estimated completion is 2011-06.

What interventions are being tested in trial NCT00233506?

The interventions under investigation include: CpG 7909 (DRUG).

Who is sponsoring clinical trial NCT00233506?

This trial is sponsored by University of Iowa, which has 228 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00233506's enrollment target sits among peer trials

41 1125th of 2000 higher than 871 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 NCT00233506, the US trial registry maintained by the National Library of Medicine. NCT00233506 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.