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Congenital Athymia Patient Registry

Recruiting · NCT05329935

Conditions: Complete DiGeorge Anomaly, Complete DiGeorge Syndrome, Congenital Athymia

At a glance

Research payments reported, 2025
$828,285
U.S. investigators named
8
Sites paid
8
Planned or actual enrollment
75

About the trial

Sponsor
Sumitomo Pharma Switzerland GmbH
Tested
Cultured Thymus Tissue (biological)
Dates
Started 2022-05-25; completion 2026-04
Results posted
Not yet

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).

From ClinicalTrials.gov, last updated 2025-08-19. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Sumitomo Pharma America, Inc. reported $828,285 in research payments for this study in 2025 (47 payments).

Products named: Rethymic

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.