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NCT00004862 · ClinicalTrials.gov registry record · Phase 1

Augmerosen Plus Fludarabine and Cytarabine in Treating Patients With Refractory or Relapsed Acute Myeloid Leukemia or Acute Lymphoblastic Leukemia

A Phase 1 study, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 1
Development phase
24
Enrollment target

NCT00004862: Completed Phase 1 study, sponsored by National Cancer Institute (NCI).

NCT00004862 is a Phase 1 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 24 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00004862, a Phase 1 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 1
Development phase
24 participants
Enrollment target

Study Summary

Phase I trial to study the effectiveness of augmerosen plus fludarabine and cytarabine in treating patients who have refractory or relapsed acute myeloid leukemia or acute lymphoblastic leukemia. Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Gene therapy such as augmerosen may make cancer cells more sensitive to chemotherapy drugs. Combining more than one drug with augmerosen may kill more cancer cells.

Interventions

  • DRUG fludarabine phosphate
  • BIOLOGICAL filgrastim
  • DRUG cytarabine
  • BIOLOGICAL oblimersen sodium

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 1999-10
Phase Phase 1
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT00004862 record still lists

NCT00004862 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower).

The record links to 0 conditions, and to 4 interventions - of which fludarabine phosphate is the first listed.

NCT00004862 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00004862 about?

NCT00004862 is a clinical study titled "Augmerosen Plus Fludarabine and Cytarabine in Treating Patients With Refractory or Relapsed Acute Myeloid Leukemia or Acute Lymphoblastic Leukemia". Phase I trial to study the effectiveness of augmerosen plus fludarabine and cytarabine in treating patients who have refractory or relapsed acute myeloid leukemia or acute lymphoblastic leukemia. Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or...

What is the current status of trial NCT00004862?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 1999-10.

What interventions are being tested in trial NCT00004862?

The interventions under investigation include: fludarabine phosphate (DRUG), filgrastim (BIOLOGICAL), cytarabine (DRUG), oblimersen sodium (BIOLOGICAL).

Who is sponsoring clinical trial NCT00004862?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00004862's enrollment target sits among peer trials

24 1520th of 2000 higher than 405 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 NCT00004862, the US trial registry maintained by the National Library of Medicine. NCT00004862 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.