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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Celecoxib for Prevention of Progression in Peutz-Jeghers SyndromeCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Cronkhite-Canada syndrome, Digestive System Diseases, Hyperpigmentation, Melanosis, Peutz-Jeghers syndrome, Skin and Connective Tissue Diseases, digestive system disorder, hereditary disease, hereditary neoplastic syndrome, intestinal disorder, lentigo, neoplasm, skin disorder, skin pigmentation disorderRecruitingNot applicable2025-05-30NCT06722534