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NCT00086125 · ClinicalTrials.gov registry record · Phase 2

Study of AP23573 in Patients With Relapsed or Refractory Hematologic Malignancies (8669-024)(COMPLETED)

A Phase 2 study of Lymphoma and Leukemia, sponsored by Merck Sharp & Dohme.

Completed
Registry status
Phase 2
Development phase
57
Enrollment target
8
Study locations

NCT00086125 is a Phase 2 study of Lymphoma and Leukemia that has completed, run by Merck Sharp & Dohme. The registered enrollment target is 57 participants, below the 484-participant average among 299 other Lymphoma trials with a reported enrollment target (88% lower). The trial reports 8 study locations across 8 states.

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The verdict

NCT00086125, a Phase 2 study of Lymphoma and Leukemia, has completed, sponsored by Merck Sharp & Dohme.

COMPLETED
Registry status
Phase 2
Development phase
57 participants
Enrollment target
8
Study locations

Study Summary

The purpose of this phase II study is to assess the efficacy of AP23573 in patients with specified relapsed or refractory hematological malignancies.

Interventions

  • DRUG ridaforolimus

Study Locations (8)

Illinois

  • University of Chicago Hospitals, Section of Hematology/Oncology - Chicago

Missouri

  • Washington University School of Medicine, Siteman Cancer Center, 4921 Parkview Place - St Louis

New Jersey

  • The Cancer Institute of New Jersey - New Brunswick

New York

  • New York Presbyterian Hospital, Weill College of Cornell University - New York

North Carolina

  • Morris Cancer Center - Duke University Medical Center, Adult Bone Marrow Transplant Clinic - Durham

Ohio

  • Gabrail Cancer Center - Canton

Pennsylvania

  • Jeane's Hospital of TUHS - Philadelphia

Texas

  • MD Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 57 participants
Start Date 2004-06
Est. Completion 2006-06
Phase Phase 2

Sponsor

Merck Sharp & Dohme

558 total trials

What the Registry Record Tells You About NCT00086125

The ClinicalTrials.gov registry entry for NCT00086125 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 57 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 484-participant average among 299 other Lymphoma trials with a reported enrollment target (88% lower). The listed sponsor is Merck Sharp & Dohme, which has 558 total studies on file at ClinicalTrials.gov.

The record links to 5 conditions, with Lymphoma appearing as the primary indexed condition, and to 1 intervention - of which ridaforolimus is the first listed.

NCT00086125 reports 8 study locations spanning 8 distinct geographic areas - top geographies include Illinois, Missouri, New Jersey.

Frequently Asked Questions

What is clinical trial NCT00086125 about?

NCT00086125 is a clinical study titled "Study of AP23573 in Patients With Relapsed or Refractory Hematologic Malignancies (8669-024)(COMPLETED)". The purpose of this phase II study is to assess the efficacy of AP23573 in patients with specified relapsed or refractory hematological malignancies.

What is the current status of trial NCT00086125?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 57 participants. The study started on 2004-06. Estimated completion is 2006-06.

What conditions does trial NCT00086125 study?

This clinical trial studies the following conditions: Lymphoma, Leukemia, Myelodysplastic Syndromes, Hematologic Malignancies, Myeloid Metaplasia.

What interventions are being tested in trial NCT00086125?

The interventions under investigation include: ridaforolimus (DRUG).

Who is sponsoring clinical trial NCT00086125?

This trial is sponsored by Merck Sharp & Dohme, which has 558 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00086125 being conducted?

This trial has 8 study locations across Illinois, Missouri, New Jersey, New York, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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.