Sickle Cell Disease Clinical Trial
Official title:
Pilot Study MUD HCT:Pts High Risk Sickle Cell,Other Non-Malignant RBC Disorders- Reduced Intensity Preparative Regimen, HAPLO-Identical Mesenchymal Stromal Cells
The main purpose of this project is to cure patients with high risk Sickle cell disease and
other red cell disorders including thalassemia and diamond-blackfan anemia by bone marrow
transplantation. The patients enrolled in this study will be those who lack matched sibling
donors and therefore have no other option but to undergo bone marrow transplantation using
matched but unrelated bone marrow or umbilical cord blood from the national marrow donor
program registry. Since bone marrow transplantation for these disorders using matched
unrelated donors has two major problems i.e. engraftment, or , the process of new marrow
being accepted and allowed to grow in the the patient; and graft-versus-host disease, or the
process where the new marrow "rejects" the host or the patient, this study has been devised
with methods to overcome these two problems and thus make transplantation from unrelated
donors both successful in terms of engraftment and safe in terms of side effects, both acute
and long term.
In order to accomplish these two goals, two important things will be done. Firstly, patients
will get three medicines which are considered reduced intensity because they are not known to
cause the serious organ damage seen with conventional chemotherapy. These medicines, however,
do cause intense immune suppression so these can cause increased infections. Secondly, in
addition to transplantation of bone marrow from unrelated donors, patients will also
transplanted with mesenchymal stromal cells derived from the bone marrow of their parents.
Mesenchymal stromal cells are adult stem cells that are normally found in the bone marrow and
are thought to create the right background for the blood cells to grow. They have been shown
in many animal and human studies to improve engraftment. In addition, they have a special
property by which they prevent and are now even considered to treat graft versus host
disease. Therefore, by using a reduced intensity chemotherapy regimen before transplant and
transplanting mesenchymal stromal cells, we hope to improve engraftment while at the same
time decrease the potential for severe side effects associated with a conventional transplant
which uses extremely high doses of chemotherapy.
n/a
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02227472 -
Working Memory and School Readiness in Preschool-Aged Children With Sickle Cell Disease
|
||
Recruiting |
NCT06301893 -
Uganda Sickle Surveillance Study (US-3)
|
||
Recruiting |
NCT04398628 -
ATHN Transcends: A Natural History Study of Non-Neoplastic Hematologic Disorders
|
||
Completed |
NCT02522104 -
Evaluation of the Impact of Renal Function on the Pharmacokinetics of SIKLOS ® (DARH)
|
Phase 4 | |
Recruiting |
NCT04688411 -
An mHealth Strategy to Improve Medication Adherence in Adolescents With Sickle Cell Disease
|
N/A | |
Terminated |
NCT03615924 -
Effect of Ticagrelor vs. Placebo in the Reduction of Vaso-occlusive Crises in Pediatric Patients With Sickle Cell Disease
|
Phase 3 | |
Not yet recruiting |
NCT06300723 -
Clinical Study of BRL-101 in Severe SCD
|
N/A | |
Recruiting |
NCT03937817 -
Collection of Human Biospecimens for Basic and Clinical Research Into Globin Variants
|
||
Completed |
NCT04917783 -
Health Literacy - Neurocognitive Screening in Pediatric SCD
|
N/A | |
Completed |
NCT04134299 -
To Assess Safety, Tolerability and Physiological Effects on Structure and Function of AXA4010 in Subjects With Sickle Cell Disease
|
N/A | |
Completed |
NCT02580565 -
Prevalence of Problematic Use of Equimolar Mixture of Oxygen and Nitrous Oxide and Analgesics in the Sickle-cell Disease
|
||
Recruiting |
NCT04754711 -
Interest of Nutritional Care of Children With Sickle Cell Disease on Bone Mineral Density and Body Composition
|
N/A | |
Completed |
NCT04388241 -
Preliminary Feasibility and Efficacy of Behavioral Intervention to Reduce Pain-Related Disability in Pediatric SCD
|
N/A | |
Recruiting |
NCT05431088 -
A Phase 2/3 Study in Adult and Pediatric Participants With SCD
|
Phase 2/Phase 3 | |
Completed |
NCT01158794 -
Genes Influencing Iron Overload State
|
||
Recruiting |
NCT03027258 -
Point-of-Delivery Prenatal Test Results Through mHealth to Improve Birth Outcome
|
N/A | |
Withdrawn |
NCT02960503 -
Macrolide Therapy to Improve Forced Expiratory Volume in 1 Second in Adults With Sickle Cell Disease
|
Phase 1/Phase 2 | |
Completed |
NCT02567695 -
A Single-Dose Relative Bioavailability Study Of GBT440 300 mg Capsules in Healthy Subjects
|
Phase 1 | |
Completed |
NCT02565082 -
Evaluation of the Hemostatic Potential in Sickle Cell Disease Patients
|
N/A | |
Not yet recruiting |
NCT02525107 -
Prevention of Vaso-occlusive Painful Crisis by Using Omega-3 Fatty Acid Supplements
|
Phase 3 |