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Study identifier: NCT05329935 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Congenital Athymia Patient Registry

Condition: Complete DiGeorge Anomaly · Complete DiGeorge Syndrome · Congenital Athymia  ·  Sponsor: Sumitomo Pharma Switzerland GmbH

PhaseN/A
Planned participants75
Who can joinAll sexes, 0 Years to 21 Years
Healthy volunteersNo

About this study

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).

This description comes directly from the study's public registry record.

Talk to the study team

John Sleasman, M.D.  ·  919-684-9914  ·  john.sleasman@duke.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Duke University School of MedicineDurham, North Carolina, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05329935