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RECRUITING
NCT05329935

Congenital Athymia Patient Registry

Sponsor: Sumitomo Pharma Switzerland GmbH

View on ClinicalTrials.gov

Summary

This Congenital Athymia Patient Registry is an observational exposure-based registry study. It uses a prospective cohort design to follow patients who have been treated with RETHYMIC. Clinical studies conducted with investigational RETHYMIC showed that treatment can result in immune reconstitution and prolong life. This treatment-based registry is being conducted to learn more about the reconstitution process following treatment and the impact of treatment on longer-term survival and the occurrence of adverse events of special interest (AESI).

Official title: Congenital Athymia Patient Registry of RETHYMIC

Key Details

Gender

All

Age Range

0 Years - 21 Years

Study Type

OBSERVATIONAL

Enrollment

75

Start Date

2022-05-25

Completion Date

2026-04

Last Updated

2025-08-19

Healthy Volunteers

Not specified

Interventions

BIOLOGICAL

Cultured Thymus Tissue

Product will be surgically administered into the quadriceps

Locations (1)

Duke University School of Medicine

Durham, North Carolina, United States