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Clinical Trial Summary

The study purpose is to determine if thymus tissue cultured in a serum-free (SF) solution is a safe and effective treatment for atypical and typical complete DiGeorge anomaly. [Funding Source - FDA OOPD]


Clinical Trial Description

Complete DiGeorge anomaly is a congenital disorder characterized by athymia. Without successful treatment, patients remain immunodeficient and usually die by age 2 years. In "typical" complete DiGeorge subjects who have no T cells, thymus transplantation without immunosuppression has resulted in diverse T cell development and good T cell function. In "atypical" complete DiGeorge subjects who have no thymus, a rash, and some T cells that presumably developed extrathymically, thymus transplantation with immunosuppression has resulted in diverse T cell development and good T cell function. Thus far, thymus transplantation studies have used thymus cultured in fetal bovine serum (FBS medium). This protocol's purpose is to determine whether transplanted thymus cultured in serum free medium can safely support thymopoiesis and T cell reconstitution as does FBS medium cultured thymus tissue in DiGeorge anomaly subjects. This protocol includes 2 arms: atypical DiGeorge subjects who will receive immunosuppression and thymus transplantation; and, typical complete DiGeorge subjects who will receive thymus transplantation without immunosuppression. Serum free medium use would reduce concerns of animal product exposure including potential exposure to bovine spongiform encephalopathy(BSE). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00849888
Study type Interventional
Source Enzyvant Therapeutics GmBH
Contact
Status Terminated
Phase Phase 1
Start date April 2008
Completion date February 2011

See also
  Status Clinical Trial Phase
Completed NCT00576836 - Thymus Transplantation Dose in DiGeorge #932 Phase 2
Completed NCT00579709 - Thymus Transplantation With Immunosuppression Phase 1
Completed NCT00579527 - Phase I/II Thymus Transplantation With Immunosuppression #950 Phase 1/Phase 2
Approved for marketing NCT01220531 - Thymus Transplantation Safety-Efficacy