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NCT01527838 · ClinicalTrials.gov registry record · Phase 1

Single Treatment With FT1050 of an Ex-vivo Modulated Umbilical Cord Blood Unit

A Phase 1 study of Chronic Lymphocytic Leukemia (CLL) and Hodgkin's Disease, sponsored by Fate Therapeutics.

Completed
Registry status
Phase 1
Development phase
10
Enrollment target
3
Study locations

NCT01527838 is a Phase 1 study of Chronic Lymphocytic Leukemia (CLL) and Hodgkin's Disease that has completed, run by Fate Therapeutics. The registered enrollment target is 10 participants, below the 191-participant average among 29 other Chronic Lymphocytic Leukemia (CLL) trials with a reported enrollment target (95% lower). The trial reports 3 study locations across 2 states.

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The verdict

NCT01527838, a Phase 1 study of Chronic Lymphocytic Leukemia (CLL) and Hodgkin's Disease, has completed, sponsored by Fate Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
10 participants
Enrollment target
3
Study locations

Study Summary

This trial is a prospective, open-label, single-arm trial of the safety of a single FT1050-treated CB unit for hematopoietic reconstitution after a reduced-intensity conditioning regimen for hematologic malignancies. A maximum of 40 eligible adult subjects will be enrolled and treated in the trial at approximately 2-4 centers within the U.S.

Interventions

  • BIOLOGICAL Single FT1050 treated UCB unit

Study Locations (3)

Massachusetts

  • Massachusetts General Hospital - Boston
  • Dana Farber Cancer Institute-Hematopoietic Stem Cell Transplant Program - Boston

Ohio

  • Ohio State Univeristy Comprehensive Cancer Center - Columbus

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2012-01
Est. Completion 2013-11
Phase Phase 1

Sponsor

Fate Therapeutics

22 total trials

What the Registry Record Tells You About NCT01527838

The ClinicalTrials.gov registry entry for NCT01527838 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 191-participant average among 29 other Chronic Lymphocytic Leukemia (CLL) trials with a reported enrollment target (95% lower). The listed sponsor is Fate Therapeutics, which has 22 total studies on file at ClinicalTrials.gov.

The record links to 5 conditions, with Chronic Lymphocytic Leukemia (CLL) appearing as the primary indexed condition, and to 1 intervention - of which Single FT1050 treated UCB unit is the first listed.

NCT01527838 reports 3 study locations spanning 2 distinct geographic areas - top geographies include Massachusetts, Ohio.

Frequently Asked Questions

What is clinical trial NCT01527838 about?

NCT01527838 is a clinical study titled "Single Treatment With FT1050 of an Ex-vivo Modulated Umbilical Cord Blood Unit". This trial is a prospective, open-label, single-arm trial of the safety of a single FT1050-treated CB unit for hematopoietic reconstitution after a reduced-intensity conditioning regimen for hematologic malignancies. A maximum of 40 eligible adult subjects will be enrolled and treated in the trial a...

What is the current status of trial NCT01527838?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 10 participants. The study started on 2012-01. Estimated completion is 2013-11.

What conditions does trial NCT01527838 study?

This clinical trial studies the following conditions: Chronic Lymphocytic Leukemia (CLL), Hodgkin's Disease, Acute Lymphoblastic Leukemia (ALL), Acute Myelogenous Leukemia (AML), Non-Hodgkins Lymphoma (NHL).

What interventions are being tested in trial NCT01527838?

The interventions under investigation include: Single FT1050 treated UCB unit (BIOLOGICAL).

Who is sponsoring clinical trial NCT01527838?

This trial is sponsored by Fate Therapeutics, which has 22 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01527838 being conducted?

This trial has 3 study locations across Massachusetts, Ohio. 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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