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NCT00620633 · ClinicalTrials.gov registry record · Phase 1

Dose Escalation Trial of WT1-Sensitized T Cells for Residual or Relapsed Leukemia After Allogeneic Hematopoietic Progenitor Cell Transplantation

A Phase 1 study of Leukemia and Myelodysplastic Syndrome, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
Phase 1
Development phase
22
Enrollment target
1
Study location

NCT00620633 is a Phase 1 study of Leukemia and Myelodysplastic Syndrome that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 22 participants, below the 487-participant average among 233 other Leukemia trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00620633, a Phase 1 study of Leukemia and Myelodysplastic Syndrome, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
Phase 1
Development phase
22 participants
Enrollment target
1
Study location

Study Summary

This study will test the safety of giving you specialized white cells from your donor. They are called WT1 sensitized T cells. They have been grown in the lab and are immunized against a protein. The protein is called the Wilms' tumor protein, or WT1. Your leukemic cells make too much of this protein. We want to learn whether the WT1 sensitized T cells will attack the protein and kill the leukemia cells.

Interventions

  • BIOLOGICAL WT1-sensitized T cells

Study Locations (1)

New York

  • Memorial Sloan Kettering Cancer Center - New York

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2008-02-08
Est. Completion 2021-02-26
Phase Phase 1

Sponsor

Memorial Sloan Kettering Cancer Center

1,884 total trials

What the Registry Record Tells You About NCT00620633

The ClinicalTrials.gov registry entry for NCT00620633 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 22 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 487-participant average among 233 other Leukemia trials with a reported enrollment target (95% lower). The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 1,884 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Leukemia appearing as the primary indexed condition, and to 1 intervention - of which WT1-sensitized T cells is the first listed.

NCT00620633 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT00620633 about?

NCT00620633 is a clinical study titled "Dose Escalation Trial of WT1-Sensitized T Cells for Residual or Relapsed Leukemia After Allogeneic Hematopoietic Progenitor Cell Transplantation". This study will test the safety of giving you specialized white cells from your donor. They are called WT1 sensitized T cells. They have been grown in the lab and are immunized against a protein. The protein is called the Wilms' tumor protein, or WT1. Your leukemic cells make too much of this protei...

What is the current status of trial NCT00620633?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 22 participants. The study started on 2008-02-08. Estimated completion is 2021-02-26.

What conditions does trial NCT00620633 study?

This clinical trial studies the following conditions: Leukemia, Myelodysplastic Syndrome.

What interventions are being tested in trial NCT00620633?

The interventions under investigation include: WT1-sensitized T cells (BIOLOGICAL).

Who is sponsoring clinical trial NCT00620633?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00620633 being conducted?

This trial has 1 study location across New York. 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

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