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NCT02757885 · ClinicalTrials.gov registry record · Phase 2

Transplantation for Patients With Sickle Cell Disease From Mismatched Family Donors of Bone Marrow

A Phase 2 study of Sickle Cell Disease, sponsored by Emory University.

Completed
Registry status
Phase 2
Development phase
10
Enrollment target
1
Study location

NCT02757885 is a Phase 2 study of Sickle Cell Disease that has completed, run by Emory University. The registered enrollment target is 10 participants, below the 293-participant average among 213 other Sickle Cell Disease trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02757885, a Phase 2 study of Sickle Cell Disease, has completed, sponsored by Emory University.

COMPLETED
Registry status
Phase 2
Development phase
10 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to learn if it is possible and safe to treat persons with severe sickle cell disease (SCD) by bone marrow transplant (BMT) from human leukocyte antigen (HLA) half-matched related donors. Preparation before transplant includes the chemotherapy drugs hydroxyurea, fludarabine, thiotepa, anti-thymocyte globulin, and cyclophosphamide. It also includes radiation.

Conditions Studied

Interventions

  • DRUG Cyclophosphamide
  • DRUG Hydroxyurea
  • DRUG Thiotepa
  • PROCEDURE Bone Marrow Transplant (BMT)
  • DRUG Fludarabine monophosphate

Study Locations (1)

Georgia

  • Children's Healthcare of Atlanta - Atlanta

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2019-07-10
Est. Completion 2021-12-14
Phase Phase 2

Sponsor

Emory University

1,208 total trials

What the Registry Record Tells You About NCT02757885

The ClinicalTrials.gov registry entry for NCT02757885 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 293-participant average among 213 other Sickle Cell Disease trials with a reported enrollment target (97% lower). The listed sponsor is Emory University, which has 1,208 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Sickle Cell Disease appearing as the primary indexed condition, and to 5 interventions - of which Cyclophosphamide is the first listed.

NCT02757885 reports 1 study location spanning 1 distinct geographic area - top geographies include Georgia.

Frequently Asked Questions

What is clinical trial NCT02757885 about?

NCT02757885 is a clinical study titled "Transplantation for Patients With Sickle Cell Disease From Mismatched Family Donors of Bone Marrow". The purpose of this study is to learn if it is possible and safe to treat persons with severe sickle cell disease (SCD) by bone marrow transplant (BMT) from human leukocyte antigen (HLA) half-matched related donors. Preparation before transplant includes the chemotherapy drugs hydroxyurea, fludarabi...

What is the current status of trial NCT02757885?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 10 participants. The study started on 2019-07-10. Estimated completion is 2021-12-14.

What conditions does trial NCT02757885 study?

This clinical trial studies the following conditions: Sickle Cell Disease.

What interventions are being tested in trial NCT02757885?

The interventions under investigation include: Cyclophosphamide (DRUG), Hydroxyurea (DRUG), Thiotepa (DRUG), Bone Marrow Transplant (BMT) (PROCEDURE), Fludarabine monophosphate (DRUG).

Who is sponsoring clinical trial NCT02757885?

This trial is sponsored by Emory University, which has 1,208 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02757885 being conducted?

This trial has 1 study location across Georgia. 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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