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COMPLETED Phase 2

A Study of Lintuzumab (SGN-33) in Combination With Low Dose Cytarabine in Patients 60+ Years With AML

NCT00528333 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to assess whether there is a survival benefit with lintuzumab given in combination with low dose cytarabine versus low dose cytarabine and placebo in patients with AML.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Lintuzumab (SGN-33)
  • DRUG Low dose cytarabine

Study Locations (20)

California

  • Tower Cancer Research Foundation — Beverly Hills
  • Glendale Memorial Hospital — Glendale
  • Kenmar Research Institute — Los Angeles
  • University of California Los Angeles — Los Angeles
  • Bay Area Cancer Research Group — Pleasant Hill

Florida

  • Lakeland Regional Cancer Center — Lakeland
  • H. Lee Moffitt Cancer Center & Research Institute — Tampa

Illinois

  • Rush University Medical Center — Chicago
  • Joliet Oncology-Hematology Associates — Joliet

New York

  • Northshore University Hospital, Monter Cancer Center — Lake Success
  • Memorial Sloan Kettering Cancer Center — New York

Alabama

  • Southern Cancer Center — Mobile

Colorado

  • University of Colorado Cancer Center — Aurora

Michigan

  • Michigan State University, Breslin Cancer Center — Lansing

Montana

  • Billings Clinic Cancer Research — Billings

Trial Details

FieldValue
Enrollment Target 211 participants
Start Date 2007-09
Est. Completion 2010-08
Phase Phase 2

Sponsor

Seagen

12 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00528333

The ClinicalTrials.gov registry entry for NCT00528333 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 211 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Seagen, which has 12 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Acute Myeloid Leukemia appearing as the primary indexed condition, and to 3 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00528333 reports 20 study locations spanning 13 distinct geographic areas — top geographies include California, Florida, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00528333 about?

NCT00528333 is a clinical study titled "A Study of Lintuzumab (SGN-33) in Combination With Low Dose Cytarabine in Patients 60+ Years With AML". The purpose of this study is to assess whether there is a survival benefit with lintuzumab given in combination with low dose cytarabine versus low dose cytarabine and placebo in patients with AML.

What is the current status of trial NCT00528333?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 211 participants. The study started on 2007-09. Estimated completion is 2010-08.

What conditions does trial NCT00528333 study?

This clinical trial studies the following conditions: Acute Myeloid Leukemia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00528333?

The interventions under investigation include: Placebo (DRUG), Lintuzumab (SGN-33) (DRUG), Low dose cytarabine (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00528333?

This trial is sponsored by Seagen, which has 12 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00528333 being conducted?

This trial has 20 study locations across Alabama, California, Colorado, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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