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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Multinational Glanzmann StudyCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Glanzmann thrombasthenia 1, Hemic and Lymphatic Diseases, blood coagulation disease, blood platelet disease, hematologic disorder, hemorrhagic disease, hereditary disease, inherited blood coagulation disorderNot yet recruitingNot stated2024-02-28NCT06204042

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UMC Utrecht140

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