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NCT00003268 · ClinicalTrials.gov registry record · Phase 1

Amifostine and Combination Chemotherapy in Treating Patients With Newly Diagnosed Acute Myeloid Leukemia

A Phase 1 study of Leukemia and Drug/Agent Toxicity by Tissue/Organ, sponsored by Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University.

Completed
Registry status
Phase 1
Development phase
1
Study location

NCT00003268: Completed Phase 1 study of Leukemia and Drug/Agent Toxicity by Tissue/Organ, sponsored by Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University.

NCT00003268 is a Phase 1 study of Leukemia and Drug/Agent Toxicity by Tissue/Organ that has completed, run by Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00003268, a Phase 1 study of Leukemia and Drug/Agent Toxicity by Tissue/Organ, has completed, sponsored by Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University.

COMPLETED
Registry status
Phase 1
Development phase
1
Study location

Study Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. Chemoprotective drugs, such as amifostine, may protect normal cells from the side effects of chemotherapy. PURPOSE: Phase I trial to study the effectiveness of amifostine in treating patients with newly diagnosed acute myeloid leukemia who are receiving idarubicin plus cytarabine.

Interventions

  • DRUG cytarabine
  • DRUG idarubicin
  • DRUG amifostine trihydrate

Study Locations (1)

Pennsylvania

  • Kimmel Cancer Center of Thomas Jefferson University - Philadelphia - Philadelphia

Trial Details

FieldValue
Start Date 1998-01
Est. Completion 2003-12
Phase Phase 1

What the finished NCT00003268 record still lists

NCT00003268 is an interventional study that assigns participants to a tested intervention. An enrollment target was not published in the registry record, which is common for early-stage or observational entries.

The record links to 2 conditions, with Leukemia appearing as the primary indexed condition, and to 3 interventions - of which cytarabine is the first listed.

NCT00003268 reports a single indexed study location in Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT00003268 about?

NCT00003268 is a clinical study titled "Amifostine and Combination Chemotherapy in Treating Patients With Newly Diagnosed Acute Myeloid Leukemia". RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. Chemoprotective drugs, such as amifostine, may protect normal cells from the side effects of chemotherapy. PURPOSE: Phase I...

What is the current status of trial NCT00003268?

This trial is currently completed. It is a Phase 1 study. The study started on 1998-01. Estimated completion is 2003-12.

What conditions does trial NCT00003268 study?

This clinical trial studies the following conditions: Leukemia, Drug/Agent Toxicity by Tissue/Organ.

What interventions are being tested in trial NCT00003268?

The interventions under investigation include: cytarabine (DRUG), idarubicin (DRUG), amifostine trihydrate (DRUG).

Who is sponsoring clinical trial NCT00003268?

This trial is sponsored by Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University, which has 138 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00003268 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT00003268, the US trial registry maintained by the National Library of Medicine. NCT00003268 (unsized enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.