Viewing Study NCT00579527


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Study NCT ID: NCT00579527
Status: COMPLETED
Last Update Posted: 2022-03-25
First Post: 2007-12-20
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: Phase I/II Thymus Transplantation With Immunosuppression #950
Sponsor: Sumitomo Pharma Switzerland GmbH
Organization:

Study Overview

Official Title: Phase I/II Trial of Thymus Transplantation With Immunosuppression, #950
Status: COMPLETED
Status Verified Date: 2022-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: #950
Brief Summary: The study purpose is to determine if cultured thymus tissue implantation (CTTI) (previously described as transplantation) with tailored immunosuppression based on the recipient's pre-implantation T cell population is a safe and effective treatment for complete DiGeorge anomaly. This study will also evaluate whether cultured thymus tissue implantation and parathyroid transplantation with immunosuppression is a safe and effective treatment for complete DiGeorge anomaly and hypoparathyroidism.
Detailed Description: Complete DiGeorge anomaly is a congenital disorder characterized by athymia. Without successful treatment, children remain immunodeficient and usually die by age 2 years. In infants with complete DiGeorge anomaly and no T cells, cultured thymus tissue implantation (CTTI) without immunosuppression resulted in diverse T cell development and good T cell function. Some infants with no thymus have some T cells that presumably developed extrathymically; these T cells can reject a thymus graft.

The purpose of this study is to tailor immunosuppression use for complete DiGeorge anomaly subjects who have some T cells and different T cell function levels. This protocol includes tailored immunosuppression regimens to allow subjects with different T cell function levels to be suppressed adequately.

Patients with complete DiGeorge often have hypoparathyroidism, a life threatening condition. Successful CTTI does not result in improvement of the hypoparathyroidism. The patients must go to the clinic for frequent calcium levels and to the hospital for calcium infusions. These infants are at risk for seizures from low calcium. This study had a parental parathyroid transplant arm for subjects with hypoparathyroidism who require calcium replacement.

Whether or not a subject was enrolled in the parathyroid arm, the immunosuppression regimen the subject received was dependent on the immune findings as stated in the clinical protocol.

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
2R01AI047040-11A2 NIH None https://reporter.nih.gov/quic… View
R56 Bridge R01AI4704011A1 OTHER_GRANT [NIH American Recovery and Reinvestment Act (ARRA) of 2009] View
5K12HD043494-09 NIH None https://reporter.nih.gov/quic… View
R01AI047040 NIH None https://reporter.nih.gov/quic… View
R01AI054843 NIH None https://reporter.nih.gov/quic… View
950 OTHER Duke View