22q11.2 deletion syndrome is a genetic disorder that can cause heart defects, facial abnormalities, and developmental and learning disabilities. The severity o…

DiGeorge Syndrome22q11.2 Deletion Syndrome

~Estimated

~$10 – $750

Albert Einstein College of MedicineNCT00556530

Phase 2

Hematopoietic Stem Cell Transplantation (HSCT) for Common Variable Immunodeficiency (CVID) and Other Autoimmune Manifestations of Primary Immune Regulatory Disorders (PIRD)

This is a research protocol that will examine Hematopoietic Stem Cell Transplantation (HSCT) using a reduced conditioning regimen (RIC) with total body Irradia…

Common Variable Immunodeficiency (CVID)Primary Immune Regulatory DisorderImmune Dysregulation+12 more

~Estimated

~$10 – $7,500

Paul SzabolcsNCT07284641

Congenital Athymia Patient Registry of RETHYMIC

This Congenital Athymia Patient Registry is an observational exposure-based registry study. It uses a prospective cohort design to follow patients who have bee…

Complete DiGeorge AnomalyComplete DiGeorge SyndromeCongenital Athymia

~Estimated

~$10 – $8,750

Sumitomo Pharma Switzerland GmbHNCT05329935