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NCT00502112 · ClinicalTrials.gov registry record · Phase 1

A Phase I Study of Lintuzumab Combined With Lenalidomide in Patients With Myelodysplastic Syndromes (MDS)

A Phase 1 study, sponsored by Seagen.

Completed
Registry status
Phase 1
Development phase
13
Enrollment target

NCT00502112: Completed Phase 1 study, sponsored by Seagen.

NCT00502112 is a Phase 1 study that has completed, run by Seagen. The registered enrollment target is 13 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (78% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00502112, a Phase 1 study, has completed, sponsored by Seagen.

COMPLETED
Registry status
Phase 1
Development phase
13 participants
Enrollment target

Study Summary

This study is a phase I, open-label, single-arm, dose escalation trial to determine the safety and activity of lenalidomide combined with lintuzumab in patients with MDS. Small groups of 3-6 patients will be treated with pre-specified doses of lenalidomide and lintuzumab and will receive 3-week cycles of combination therapy.

Interventions

  • DRUG lenalidomide
  • DRUG lintuzumab

Trial Details

FieldValue
Enrollment Target 13 participants
Start Date 2008-03
Est. Completion 2010-05
Phase Phase 1
Seagen

84 total trials

What the finished NCT00502112 record still lists

NCT00502112 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 13 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (78% lower).

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

NCT00502112 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00502112 about?

NCT00502112 is a clinical study titled "A Phase I Study of Lintuzumab Combined With Lenalidomide in Patients With Myelodysplastic Syndromes (MDS)". This study is a phase I, open-label, single-arm, dose escalation trial to determine the safety and activity of lenalidomide combined with lintuzumab in patients with MDS. Small groups of 3-6 patients will be treated with pre-specified doses of lenalidomide and lintuzumab and will receive 3-week cycl...

What is the current status of trial NCT00502112?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 13 participants. The study started on 2008-03. Estimated completion is 2010-05.

What interventions are being tested in trial NCT00502112?

The interventions under investigation include: lenalidomide (DRUG), lintuzumab (DRUG).

Who is sponsoring clinical trial NCT00502112?

This trial is sponsored by Seagen, which has 84 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00502112's enrollment target sits among peer trials

13 1847th of 2000 higher than 149 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 NCT00502112, the US trial registry maintained by the National Library of Medicine. NCT00502112 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.