Expanded Access Protocol Thymus Transplantation for Immunodeficiency, Hematologic Malignancies, and Autoimmune Disease Related to Poor Thymic Function

Status: Completed
Intervention Type: Drug, Procedure, Biological
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

The primary purpose is to provide access for patients who have immunodeficiency or severe autoimmune disease related to poor thymic function to cultured thymus tissue for implantation. With no thymus function, bone marrow stem cells do not develop into educated T cells, which fight infection. Eligible participants receive cultured thymus tissue for implantation and may undergo biopsy. Immune suppression may be given depending on the immune status and clinical condition of the participant. Immune function testing is continued for one year post-implantation.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• an immunodeficiency or severe autoimmunity for which development of naïve T cells would be expected to lead to lead to clinical improvement.

• written consent (or consent of parent/legal guardian as applicable), review of medical testing, laboratory studies, and physical examinations are used to determine whether the patient is clinically stable and will potentially benefit from receiving cultured thymus tissue. Each participant is reviewed with the Data Safety and Monitoring Board (DSMB).

Time Frame
Start Date: 2014-08
Completion Date: 2023-08
Participants
Target number of participants: 11
Treatments
Experimental: Cultured thymus tissue implantation (CTTI)
Cultured thymus tissue for the treatment of immunodeficiency and autoimmune disorders
Sponsors
Leads: Sumitomo Pharma Switzerland GmbH

This content was sourced from clinicaltrials.gov