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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Li-Fraumeni Syndrome/TP53 BiobankCongenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA repair disease, Li-Fraumeni syndrome, Li-fraumeni-like syndrome, Nutritional and Metabolic Diseases, hereditary disease, hereditary neoplastic syndrome, metabolic disease, neoplasmRecruitingNot stated2026-09-04NCT04367246

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2 results · Page 1 of 1

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Research sitesCityCountryLinked trials
Children's Hospital of PhiladelphiaPhildelphiaUnited States1
University of PennsylvaniaPhiladelphiaUnited States507