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NCT00103558 · ClinicalTrials.gov registry record · Phase 1

Lumiliximab in Combination With FCR in Subjects With Relapsed Chronic Lymphocytic Leukemia (CLL)

A Phase 1 study, sponsored by Biogen.

Completed
Registry status
Phase 1
Development phase
31
Enrollment target

NCT00103558 is a Phase 1 study that has completed, run by Biogen. The registered enrollment target is 31 participants.

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The verdict

NCT00103558, a Phase 1 study, has completed, sponsored by Biogen.

COMPLETED
Registry status
Phase 1
Development phase
31 participants
Enrollment target

Study Summary

This is an open label, Phase I/II, dose escalation research study of an investigational product called lumiliximab, given with FDA (Food and Drug Administration) approved products fludarabine, cyclophosphamide, and rituximab (FCR). The study duration is 17 visits over 42 months or until your disease progresses and you require additional CLL therapy. The total duration of participation in the study will be approximately 4 years, however your disease status will be followed indefinitely (forever).

Interventions

  • DRUG Lumiliximab with FCR

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2004-03
Est. Completion 2010-03
Phase Phase 1

Sponsor

Biogen

334 total trials

What the Registry Record Tells You About NCT00103558

The ClinicalTrials.gov registry entry for NCT00103558 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Biogen, which has 334 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Lumiliximab with FCR is the first listed.

NCT00103558 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00103558 about?

NCT00103558 is a clinical study titled "Lumiliximab in Combination With FCR in Subjects With Relapsed Chronic Lymphocytic Leukemia (CLL)". This is an open label, Phase I/II, dose escalation research study of an investigational product called lumiliximab, given with FDA (Food and Drug Administration) approved products fludarabine, cyclophosphamide, and rituximab (FCR). The study duration is 17 visits over 42 months or until your disease...

What is the current status of trial NCT00103558?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 31 participants. The study started on 2004-03. Estimated completion is 2010-03.

What interventions are being tested in trial NCT00103558?

The interventions under investigation include: Lumiliximab with FCR (DRUG).

Who is sponsoring clinical trial NCT00103558?

This trial is sponsored by Biogen, which has 334 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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, or report a data error.