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NCT00486265 · ClinicalTrials.gov registry record · Phase 1

Phase I/II, Open-label, Multi-center, Two Part Dose-escalation, Safety, Pharmacokinetics (PK) and Efficacy Study of AZD4877 in Patients With Acute Myelogenous Leukemia (AML)

A Phase 1 study, sponsored by AstraZeneca.

Terminated
Registry status
Phase 1
Development phase
47
Enrollment target

NCT00486265 is a Phase 1 study that was terminated before completion, run by AstraZeneca. The registered enrollment target is 47 participants.

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The verdict

NCT00486265, a Phase 1 study, was terminated before completion, sponsored by AstraZeneca.

TERMINATED
Registry status
Phase 1
Development phase
47 participants
Enrollment target

Study Summary

The primary purpose of this study is to find out what the maximum tolerated dose is for an experimental drug called AZD4877 based on the side effects experienced by patients that receive AZD4877 on a daily times 3 schedule in acute myelogenous leukemia (AML). For enrollment information see the Central Contact information below

Interventions

  • DRUG AZD4877

Trial Details

FieldValue
Enrollment Target 47 participants
Start Date 2007-07
Est. Completion 2009-07
Phase Phase 1

Sponsor

AstraZeneca

1,285 total trials

What the Registry Record Tells You About NCT00486265

The ClinicalTrials.gov registry entry for NCT00486265 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 47 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AstraZeneca, which has 1,285 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which AZD4877 is the first listed.

NCT00486265 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00486265 about?

NCT00486265 is a clinical study titled "Phase I/II, Open-label, Multi-center, Two Part Dose-escalation, Safety, Pharmacokinetics (PK) and Efficacy Study of AZD4877 in Patients With Acute Myelogenous Leukemia (AML)". The primary purpose of this study is to find out what the maximum tolerated dose is for an experimental drug called AZD4877 based on the side effects experienced by patients that receive AZD4877 on a daily times 3 schedule in acute myelogenous leukemia (AML). For enrollment information see the Cent...

What is the current status of trial NCT00486265?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 47 participants. The study started on 2007-07. Estimated completion is 2009-07.

What interventions are being tested in trial NCT00486265?

The interventions under investigation include: AZD4877 (DRUG).

Who is sponsoring clinical trial NCT00486265?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

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

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.