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NCT00002609 · ClinicalTrials.gov registry record · Phase 2

Monoclonal Antibody Therapy and Chemotherapy in Treating Patients With Acute Promyelocytic Leukemia in Remission

A Phase 2 study, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
Phase 2
Development phase
40
Enrollment target

NCT00002609: Completed Phase 2 study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT00002609 is a Phase 2 study that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 40 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00002609, a Phase 2 study, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
40 participants
Enrollment target

Study Summary

RATIONALE: Monoclonal antibodies can locate cancer cells and either kill them or deliver tumor-killing substances to them, without harming normal cells. Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Combining chemotherapy with monoclonal antibody therapy may kill more cancer cells. PURPOSE: Phase II trial to study the effectiveness of chemotherapy plus monoclonal antibody therapy in treating patients with acute promyelocytic leukemia in remission.

Interventions

  • DRUG cytarabine
  • DRUG idarubicin
  • BIOLOGICAL lintuzumab

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 1994-08
Est. Completion 2003-02
Phase Phase 2
Memorial Sloan Kettering Cancer Center

1,884 total trials

What the finished NCT00002609 record still lists

NCT00002609 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower).

The record links to 0 conditions, and to 3 interventions - of which cytarabine is the first listed.

NCT00002609 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00002609 about?

NCT00002609 is a clinical study titled "Monoclonal Antibody Therapy and Chemotherapy in Treating Patients With Acute Promyelocytic Leukemia in Remission". RATIONALE: Monoclonal antibodies can locate cancer cells and either kill them or deliver tumor-killing substances to them, without harming normal cells. Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Combining chemotherapy with monoclona...

What is the current status of trial NCT00002609?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 1994-08. Estimated completion is 2003-02.

What interventions are being tested in trial NCT00002609?

The interventions under investigation include: cytarabine (DRUG), idarubicin (DRUG), lintuzumab (BIOLOGICAL).

Who is sponsoring clinical trial NCT00002609?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00002609's enrollment target sits among peer trials

40 1362nd of 2000 higher than 542 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 NCT00002609, the US trial registry maintained by the National Library of Medicine. NCT00002609 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.