Clinical Trials Directory

Trials / Terminated

TerminatedNCT00278642

Hematopoietic Stem Cell Support in Patients With Autoimmune Bullous Skin Disorders

High Dose Cyclophosphamide & ATG With Hematopoietic Stem Cell Support in Patients With Autoimmune Bullous Skin Disorders: A Phase I Trial

Status
Terminated
Phase
Phase 1
Study type
Interventional
Enrollment
1 (actual)
Sponsor
Richard Burt, MD · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Autoimmune Bullous Skin Disorders are believed to be due to immune cells, cells that normally protect the body and are now causing damage to the body. This study is designed to examine whether treating patients with high dose cyclophosphamide (a drug which reduces the function of the immune system) together with anti-thymocyte globulin (a protein that kills the immune cells that are thought to be causing your disease), followed by return of the previously collected special blood cells (stem cells) will result in improvement of this disease. Stem cells are undeveloped cells that have the capacity to grow into mature blood cells, which normally circulate in the blood stream. The purpose of the intense chemotherapy is to destroy the cells in the immune system which may be causing this skin disease. The purpose of the stem cell infusion is to restore the body's blood production, which will be severely impaired by the high dose chemotherapy and anti-thymocyte globulin.

Conditions

Interventions

TypeNameDescription
BIOLOGICALHematopoietic stem cell transplantationAutologous hematopoietic stem cell transplantation

Timeline

Start date
2002-09-01
Primary completion
2011-09-01
Completion
2011-09-01
First posted
2006-01-18
Last updated
2013-04-08

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00278642. Inclusion in this directory is not an endorsement.