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
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | Hematopoietic stem cell transplantation | Autologous 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.